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<ValueSet xmlns="http://hl7.org/fhir">
  <id value="ValueSet-Genomics-ConditionCode-1" />
  <url value="https://simplifier.net/genomicsfhirprofiles/valueset-genomics-conditioncode-1" />
  <version value="1.0.0" />
  <name value="ValueSet-Genomics-ConditionCode-1" />
  <status value="draft" />
  <publisher value="NHS Digital" />
  <contact>
    <name value="Interoperability Team" />
    <telecom>
      <system value="email" />
      <value value="interoperabilityteam@nhs.net" />
      <use value="work" />
    </telecom>
  </contact>
  <description value="A ValueSet that contains a set of codes that describes the condition." />
  <copyright value="Copyright © 2018 NHS Digital" />
  <compose>
    <include>
      <system value="https://simplifier.net/genomicsfhirprofiles/codesystem-genomics-conditioncode-1" />
      <concept>
        <code value="OMIM:no_specific_disorder" />
        <display value="NO SPECIFIC DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:100050" />
        <display value="AARSKOG SYNDROME, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:100070" />
        <display value="AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:100100" />
        <display value="PRUNE BELLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:100200" />
        <display value="ABDUCENS PALSY" />
      </concept>
      <concept>
        <code value="OMIM:100300" />
        <display value="ADAMS-OLIVER SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:100600" />
        <display value="ACANTHOSIS NIGRICANS" />
      </concept>
      <concept>
        <code value="OMIM:100650" />
        <display value="ALDEHYDE DEHYDROGENASE 2 FAMILY" />
      </concept>
      <concept>
        <code value="OMIM:100675" />
        <display value="ACETAMINOPHEN METABOLISM" />
      </concept>
      <concept>
        <code value="OMIM:100700" />
        <display value="ACHARD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:100800" />
        <display value="ACHONDROPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:100820" />
        <display value="ACHOO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:101000" />
        <display value="NEUROFIBROMATOSIS, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:101120" />
        <display value="ACROCEPHALOPOLYSYNDACTYLY TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:101200" />
        <display value="APERT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:101400" />
        <display value="SAETHRE-CHOTZEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:101600" />
        <display value="PFEIFFER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:101800" />
        <display value="ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:101805" />
        <display value="ACROFACIAL DYSOSTOSIS, CATANIA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:101840" />
        <display value="ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT" />
      </concept>
      <concept>
        <code value="OMIM:101850" />
        <display value="PALMOPLANTAR KERATODERMA, PUNCTATE TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:101900" />
        <display value="ACROKERATOSIS VERRUCIFORMIS" />
      </concept>
      <concept>
        <code value="OMIM:102000" />
        <display value="ACROLEUKOPATHY, SYMMETRIC" />
      </concept>
      <concept>
        <code value="OMIM:102100" />
        <display value="ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA" />
      </concept>
      <concept>
        <code value="OMIM:102150" />
        <display value="ACROMEGALOID FACIAL APPEARANCE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:102200" />
        <display value="PITUITARY ADENOMA 1, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:102300" />
        <display value="RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:102350" />
        <display value="ACROMIAL DIMPLES" />
      </concept>
      <concept>
        <code value="OMIM:102370" />
        <display value="ACROMICRIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:102400" />
        <display value="ACROOSTEOLYSIS" />
      </concept>
      <concept>
        <code value="OMIM:102500" />
        <display value="HAJDU-CHENEY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:102510" />
        <display value="ACROPECTOROVERTEBRAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:102520" />
        <display value="ACRORENAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:102530" />
        <display value="SPERMATOGENIC FAILURE 6" />
      </concept>
      <concept>
        <code value="OMIM:102590" />
        <display value="ACYLASE, COBALT-ACTIVATED" />
      </concept>
      <concept>
        <code value="OMIM:102650" />
        <display value="ADACTYLIA, UNILATERAL" />
      </concept>
      <concept>
        <code value="OMIM:102660" />
        <display value="ADAMANTINOMA OF LONG BONES" />
      </concept>
      <concept>
        <code value="OMIM:102699" />
        <display value="ADENO-ASSOCIATED VIRUS INTEGRATION SITE 1" />
      </concept>
      <concept>
        <code value="OMIM:102700" />
        <display value="SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:102730" />
        <display value="ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:102800" />
        <display value="ADENOSINE TRIPHOSPHATASE DEFICIENCY, ANEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:102900" />
        <display value="ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES" />
      </concept>
      <concept>
        <code value="OMIM:103050" />
        <display value="ADENYLOSUCCINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:103100" />
        <display value="ADIE PUPIL" />
      </concept>
      <concept>
        <code value="OMIM:103200" />
        <display value="ADIPOSIS DOLOROSA" />
      </concept>
      <concept>
        <code value="OMIM:103230" />
        <display value="ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:103285" />
        <display value="ADULT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:103300" />
        <display value="HYPOGLOSSIA-HYPODACTYLIA" />
      </concept>
      <concept>
        <code value="OMIM:103400" />
        <display value="AINHUM" />
      </concept>
      <concept>
        <code value="OMIM:103420" />
        <display value="ALACRIMA, CONGENITAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:103470" />
        <display value="ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:103500" />
        <display value="TIETZ ALBINISM-DEAFNESS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:103580" />
        <display value="PSEUDOHYPOPARATHYROIDISM, TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:103780" />
        <display value="ALCOHOL DEPENDENCE" />
      </concept>
      <concept>
        <code value="OMIM:103900" />
        <display value="HYPERALDOSTERONISM, FAMILIAL, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:103920" />
        <display value="ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:104000" />
        <display value="ALOPECIA AREATA 1" />
      </concept>
      <concept>
        <code value="OMIM:104100" />
        <display value="PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1" />
      </concept>
      <concept>
        <code value="OMIM:104110" />
        <display value="ALOPECIA, FAMILIAL FOCAL" />
      </concept>
      <concept>
        <code value="OMIM:104130" />
        <display value="ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY" />
      </concept>
      <concept>
        <code value="OMIM:104200" />
        <display value="ALPORT SYNDROME, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:104250" />
        <display value="ALPHA-2C-ADRENERGIC RECEPTOR" />
      </concept>
      <concept>
        <code value="OMIM:104290" />
        <display value="ALTERNATING HEMIPLEGIA OF CHILDHOOD 1" />
      </concept>
      <concept>
        <code value="OMIM:104300" />
        <display value="ALZHEIMER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:104310" />
        <display value="ALZHEIMER DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:104350" />
        <display value="AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:104400" />
        <display value="AMELIA AND TERMINAL TRANSVERSE HEMIMELIA" />
      </concept>
      <concept>
        <code value="OMIM:104500" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IB" />
      </concept>
      <concept>
        <code value="OMIM:104510" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:104530" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:104570" />
        <display value="AMELOONYCHOHYPOHIDROTIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:104600" />
        <display value="AMENORRHEA-GALACTORRHEA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:105120" />
        <display value="AMYLOIDOSIS, FINNISH TYPE" />
      </concept>
      <concept>
        <code value="OMIM:105150" />
        <display value="CEREBRAL AMYLOID ANGIOPATHY, CST3-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:105200" />
        <display value="AMYLOIDOSIS, FAMILIAL VISCERAL" />
      </concept>
      <concept>
        <code value="OMIM:105210" />
        <display value="AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:105250" />
        <display value="AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1" />
      </concept>
      <concept>
        <code value="OMIM:105300" />
        <display value="AMYOTROPHIC DYSTONIC PARAPLEGIA" />
      </concept>
      <concept>
        <code value="OMIM:105400" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:105500" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1" />
      </concept>
      <concept>
        <code value="OMIM:105550" />
        <display value="FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:105563" />
        <display value="ANAL SPHINCTER DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:105565" />
        <display value="ANAL SPHINCTER MYOPATHY, INTERNAL" />
      </concept>
      <concept>
        <code value="OMIM:105570" />
        <display value="ANDROSTENONE, ABILITY TO SMELL" />
      </concept>
      <concept>
        <code value="OMIM:105580" />
        <display value="ANAL CANAL CARCINOMA" />
      </concept>
      <concept>
        <code value="OMIM:105600" />
        <display value="ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:105650" />
        <display value="DIAMOND-BLACKFAN ANEMIA 1" />
      </concept>
      <concept>
        <code value="OMIM:105800" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 1" />
      </concept>
      <concept>
        <code value="OMIM:105805" />
        <display value="ANEURYSM OF INTERVENTRICULAR SEPTUM" />
      </concept>
      <concept>
        <code value="OMIM:105830" />
        <display value="ANGELMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:105835" />
        <display value="ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:106050" />
        <display value="ANGIOMA SERPIGINOSUM, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:106070" />
        <display value="ANGIOMA, HEREDITARY NEUROCUTANEOUS" />
      </concept>
      <concept>
        <code value="OMIM:106100" />
        <display value="ANGIOEDEMA, HEREDITARY, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:106150" />
        <display value="ANGIOTENSINOGEN" />
      </concept>
      <concept>
        <code value="OMIM:106180" />
        <display value="ANGIOTENSIN I-CONVERTING ENZYME" />
      </concept>
      <concept>
        <code value="OMIM:106190" />
        <display value="ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS" />
      </concept>
      <concept>
        <code value="OMIM:106210" />
        <display value="ANIRIDIA 1" />
      </concept>
      <concept>
        <code value="OMIM:106220" />
        <display value="ANIRIDIA AND ABSENT PATELLA" />
      </concept>
      <concept>
        <code value="OMIM:106230" />
        <display value="ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT" />
      </concept>
      <concept>
        <code value="OMIM:106240" />
        <display value="ANISOCORIA" />
      </concept>
      <concept>
        <code value="OMIM:106250" />
        <display value="ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE" />
      </concept>
      <concept>
        <code value="OMIM:106260" />
        <display value="ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE" />
      </concept>
      <concept>
        <code value="OMIM:106280" />
        <display value="ANKYLOGLOSSIA" />
      </concept>
      <concept>
        <code value="OMIM:106300" />
        <display value="SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:106400" />
        <display value="ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSIS" />
      </concept>
      <concept>
        <code value="OMIM:106500" />
        <display value="ANNULAR ERYTHEMA" />
      </concept>
      <concept>
        <code value="OMIM:106600" />
        <display value="TOOTH AGENESIS, SELECTIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:106700" />
        <display value="TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1" />
      </concept>
      <concept>
        <code value="OMIM:106750" />
        <display value="ANONYCHIA WITH FLEXURAL PIGMENTATION" />
      </concept>
      <concept>
        <code value="OMIM:106900" />
        <display value="ANONYCHIA-ECTRODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:106990" />
        <display value="ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:106995" />
        <display value="ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES" />
      </concept>
      <concept>
        <code value="OMIM:107000" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:107100" />
        <display value="ANORECTAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:107200" />
        <display value="ANOSMIA, ISOLATED CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:107250" />
        <display value="ANTERIOR SEGMENT DYSGENESIS 1" />
      </concept>
      <concept>
        <code value="OMIM:107290" />
        <display value="ANTIPYRINE METABOLISM" />
      </concept>
      <concept>
        <code value="OMIM:107320" />
        <display value="ANTIPHOSPHOLIPID SYNDROME, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:107410" />
        <display value="SERPIN PEPTIDASE INHIBITOR, CLADE A, MEMBER 2, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:107440" />
        <display value="ANTIVIRAL STATE REPRESSOR, REGULATOR OF" />
      </concept>
      <concept>
        <code value="OMIM:107480" />
        <display value="TOWNES-BROCKS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:107500" />
        <display value="AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:107550" />
        <display value="AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA" />
      </concept>
      <concept>
        <code value="OMIM:107600" />
        <display value="APLASIA CUTIS CONGENITA, NONSYNDROMIC" />
      </concept>
      <concept>
        <code value="OMIM:107640" />
        <display value="APNEA, CENTRAL SLEEP" />
      </concept>
      <concept>
        <code value="OMIM:107650" />
        <display value="APNEA, OBSTRUCTIVE SLEEP" />
      </concept>
      <concept>
        <code value="OMIM:107670" />
        <display value="APOLIPOPROTEIN A-II" />
      </concept>
      <concept>
        <code value="OMIM:107680" />
        <display value="APOLIPOPROTEIN A-I" />
      </concept>
      <concept>
        <code value="OMIM:107700" />
        <display value="APPENDICITIS, PRONENESS TO" />
      </concept>
      <concept>
        <code value="OMIM:107730" />
        <display value="APOLIPOPROTEIN B" />
      </concept>
      <concept>
        <code value="OMIM:107750" />
        <display value="ARBITRARY RESTRICTION POLYMORPHISM 1" />
      </concept>
      <concept>
        <code value="OMIM:107800" />
        <display value="ARCUS CORNEAE" />
      </concept>
      <concept>
        <code value="OMIM:107850" />
        <display value="ARM FOLDING PREFERENCE" />
      </concept>
      <concept>
        <code value="OMIM:107900" />
        <display value="ARMS, MALFORMATION OF" />
      </concept>
      <concept>
        <code value="OMIM:107920" />
        <display value="AROMATIC ALPHA-KETO ACID REDUCTASE" />
      </concept>
      <concept>
        <code value="OMIM:107970" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:108000" />
        <display value="ARTERIES, ANOMALIES OF" />
      </concept>
      <concept>
        <code value="OMIM:108010" />
        <display value="ARTERIOVENOUS MALFORMATIONS OF THE BRAIN" />
      </concept>
      <concept>
        <code value="OMIM:108050" />
        <display value="ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS" />
      </concept>
      <concept>
        <code value="OMIM:108100" />
        <display value="ARTHRITIS, SACROILIAC" />
      </concept>
      <concept>
        <code value="OMIM:108120" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 1A" />
      </concept>
      <concept>
        <code value="OMIM:108145" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:108200" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:108300" />
        <display value="STICKLER SYNDROME, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:108320" />
        <display value="ARTICHOKE, MODIFICATION OF TASTE BY" />
      </concept>
      <concept>
        <code value="OMIM:108340" />
        <display value="ARYL HYDROCARBON HYDROXYLASE INDUCIBILITY" />
      </concept>
      <concept>
        <code value="OMIM:108390" />
        <display value="ASPARAGUS, SPECIFIC SMELL HYPERSENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:108420" />
        <display value="SPERMATOGENIC FAILURE 2" />
      </concept>
      <concept>
        <code value="OMIM:108450" />
        <display value="ASYMMETRIC SHORT STATURE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:108500" />
        <display value="EPISODIC ATAXIA, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:108600" />
        <display value="SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:108650" />
        <display value="SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:108700" />
        <display value="ATAXIA WITH FASCICULATIONS" />
      </concept>
      <concept>
        <code value="OMIM:108720" />
        <display value="ATELOSTEOGENESIS, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:108721" />
        <display value="ATELOSTEOGENESIS, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:108725" />
        <display value="ATHEROSCLEROSIS SUSCEPTIBILITY" />
      </concept>
      <concept>
        <code value="OMIM:108760" />
        <display value="ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTIVE DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:108770" />
        <display value="ATRIAL STANDSTILL 1" />
      </concept>
      <concept>
        <code value="OMIM:108800" />
        <display value="ATRIAL SEPTAL DEFECT 1" />
      </concept>
      <concept>
        <code value="OMIM:108900" />
        <display value="ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:108950" />
        <display value="ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL" />
      </concept>
      <concept>
        <code value="OMIM:108980" />
        <display value="PR INTERVAL, VARIATION IN" />
      </concept>
      <concept>
        <code value="OMIM:108985" />
        <display value="SVEINSSON CHORIORETINAL ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:109000" />
        <display value="AURICULOOSTEODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:109050" />
        <display value="AUROCEPHALOSYNDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:109100" />
        <display value="AUTOIMMUNE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:109120" />
        <display value="AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:109130" />
        <display value="AXIAL OSTEOMALACIA" />
      </concept>
      <concept>
        <code value="OMIM:109150" />
        <display value="MACHADO-JOSEPH DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:109160" />
        <display value="AZOTEMIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:109180" />
        <display value="BABOON M7 VIRUS INTEGRATION SITE" />
      </concept>
      <concept>
        <code value="OMIM:109200" />
        <display value="ALOPECIA, ANDROGENETIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:109270" />
        <display value="SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1" />
      </concept>
      <concept>
        <code value="OMIM:109300" />
        <display value="BANKI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:109350" />
        <display value="GASTROESOPHAGEAL REFLUX" />
      </concept>
      <concept>
        <code value="OMIM:109400" />
        <display value="BASAL CELL NEVUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:109500" />
        <display value="BASILAR IMPRESSION, PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:109540" />
        <display value="B-CELL GROWTH FACTOR" />
      </concept>
      <concept>
        <code value="OMIM:109543" />
        <display value="LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:109600" />
        <display value="BEETURIA" />
      </concept>
      <concept>
        <code value="OMIM:109630" />
        <display value="BETA-1-ADRENERGIC RECEPTOR" />
      </concept>
      <concept>
        <code value="OMIM:109650" />
        <display value="BEHCET SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:109660" />
        <display value="BETA-AMINO ACIDS, RENAL TRANSPORT OF" />
      </concept>
      <concept>
        <code value="OMIM:109670" />
        <display value="BETA-ADRENERGIC STIMULATION, RESPONSE TO" />
      </concept>
      <concept>
        <code value="OMIM:109690" />
        <display value="BETA-2-ADRENERGIC RECEPTOR" />
      </concept>
      <concept>
        <code value="OMIM:109720" />
        <display value="BILIARY CIRRHOSIS, PRIMARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:109730" />
        <display value="AORTIC VALVE DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:109740" />
        <display value="BIFID NOSE, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:109800" />
        <display value="BLADDER CANCER" />
      </concept>
      <concept>
        <code value="OMIM:109820" />
        <display value="BLADDER DIVERTICULUM" />
      </concept>
      <concept>
        <code value="OMIM:109900" />
        <display value="BLEPHAROCHALASIS AND DOUBLE LIP" />
      </concept>
      <concept>
        <code value="OMIM:110000" />
        <display value="BLEPHAROCHALASIS, SUPERIOR" />
      </concept>
      <concept>
        <code value="OMIM:110050" />
        <display value="BLEPHARONASOFACIAL MALFORMATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:110100" />
        <display value="BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS" />
      </concept>
      <concept>
        <code value="OMIM:110150" />
        <display value="BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS" />
      </concept>
      <concept>
        <code value="OMIM:110250" />
        <display value="BLOOD GROUP--ABO SUPPRESSOR" />
      </concept>
      <concept>
        <code value="OMIM:110310" />
        <display value="BLOOD GROUP--ABH ANTIGEN, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:110350" />
        <display value="BLOOD GROUP--AHONEN" />
      </concept>
      <concept>
        <code value="OMIM:110450" />
        <display value="BLOOD GROUP, COLTON SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:110500" />
        <display value="BLOOD GROUP, DIEGO SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:110700" />
        <display value="BLOOD GROUP, DUFFY SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:110720" />
        <display value="BLOOD GROUP--En" />
      </concept>
      <concept>
        <code value="OMIM:110800" />
        <display value="BLOOD GROUP, I SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:110900" />
        <display value="BLOOD GROUP--KELL SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:111000" />
        <display value="BLOOD GROUP, KIDD SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:111100" />
        <display value="FUCOSYLTRANSFERASE 3" />
      </concept>
      <concept>
        <code value="OMIM:111130" />
        <display value="BLOOD GROUP--LKE" />
      </concept>
      <concept>
        <code value="OMIM:111150" />
        <display value="BLOOD GROUP--LUTHERAN INHIBITOR" />
      </concept>
      <concept>
        <code value="OMIM:111200" />
        <display value="BLOOD GROUP--LUTHERAN SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:111250" />
        <display value="BLOOD GROUP SYSTEM, LANDSTEINER-WIENER" />
      </concept>
      <concept>
        <code value="OMIM:111300" />
        <display value="BLOOD GROUP, MN" />
      </concept>
      <concept>
        <code value="OMIM:111360" />
        <display value="BLOOD GROUP--NEWFOUNDLAND" />
      </concept>
      <concept>
        <code value="OMIM:111380" />
        <display value="BLOOD GROUP--OK" />
      </concept>
      <concept>
        <code value="OMIM:111400" />
        <display value="BLOOD GROUP, P1PK SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:111500" />
        <display value="BLOOD GROUP--PRIVATE SYSTEMS" />
      </concept>
      <concept>
        <code value="OMIM:111600" />
        <display value="BLOOD GROUP, LANGEREIS SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:111620" />
        <display value="RADIN BLOOD GROUP ANTIGEN" />
      </concept>
      <concept>
        <code value="OMIM:111740" />
        <display value="BLOOD GROUP, Ss" />
      </concept>
      <concept>
        <code value="OMIM:111750" />
        <display value="BLOOD GROUP--SCIANNA SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:111800" />
        <display value="BLOOD GROUP--STOLTZFUS SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:112000" />
        <display value="BLOOD GROUP--Ul SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:112010" />
        <display value="BLOOD GROUP--WALDNER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:112050" />
        <display value="BLOOD GROUP--WRIGHT ANTIGEN" />
      </concept>
      <concept>
        <code value="OMIM:112100" />
        <display value="YT BLOOD GROUP ANTIGEN" />
      </concept>
      <concept>
        <code value="OMIM:112200" />
        <display value="BLUE RUBBER BLEB NEVUS" />
      </concept>
      <concept>
        <code value="OMIM:112240" />
        <display value="COLE-CARPENTER SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:112250" />
        <display value="DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA" />
      </concept>
      <concept>
        <code value="OMIM:112270" />
        <display value="BONE PAIN, PERIODIC" />
      </concept>
      <concept>
        <code value="OMIM:112300" />
        <display value="BOOK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:112310" />
        <display value="BOOMERANG DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:112350" />
        <display value="WEISMANN-NETTER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:112370" />
        <display value="BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUS ADDUCTUS, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:112410" />
        <display value="HYPERTENSION AND BRACHYDACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:112430" />
        <display value="LONG-THUMB BRACHYDACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:112440" />
        <display value="BRACHYDACTYLY, COMBINED B AND E TYPES" />
      </concept>
      <concept>
        <code value="OMIM:112450" />
        <display value="BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION" />
      </concept>
      <concept>
        <code value="OMIM:112500" />
        <display value="BRACHYDACTYLY, TYPE A1" />
      </concept>
      <concept>
        <code value="OMIM:112600" />
        <display value="BRACHYDACTYLY, TYPE A2" />
      </concept>
      <concept>
        <code value="OMIM:112700" />
        <display value="BRACHYDACTYLY, TYPE A3" />
      </concept>
      <concept>
        <code value="OMIM:112800" />
        <display value="BRACHYDACTYLY, TYPE A4" />
      </concept>
      <concept>
        <code value="OMIM:112910" />
        <display value="OSEBOLD-REMONDINI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:113000" />
        <display value="BRACHYDACTYLY, TYPE B1" />
      </concept>
      <concept>
        <code value="OMIM:113100" />
        <display value="BRACHYDACTYLY, TYPE C" />
      </concept>
      <concept>
        <code value="OMIM:113200" />
        <display value="BRACHYDACTYLY, TYPE D" />
      </concept>
      <concept>
        <code value="OMIM:113300" />
        <display value="BRACHYDACTYLY, TYPE E1" />
      </concept>
      <concept>
        <code value="OMIM:113301" />
        <display value="BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:113310" />
        <display value="BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:113400" />
        <display value="BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:113450" />
        <display value="BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:113470" />
        <display value="BRACHYMESOMELIA-RENAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:113475" />
        <display value="BRACHYMETATARSUS IV" />
      </concept>
      <concept>
        <code value="OMIM:113477" />
        <display value="BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:113480" />
        <display value="BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:113500" />
        <display value="BRACHYOLMIA TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:113600" />
        <display value="BRANCHIAL CLEFT ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:113610" />
        <display value="BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:113620" />
        <display value="BRANCHIOOCULOFACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:113650" />
        <display value="BRANCHIOOTORENAL SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:113670" />
        <display value="HYPERTROPHY OF THE BREAST, JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:113700" />
        <display value="BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1" />
      </concept>
      <concept>
        <code value="OMIM:113721" />
        <display value="BREAST CANCER-RELATED REGULATOR OF TP53" />
      </concept>
      <concept>
        <code value="OMIM:113750" />
        <display value="ALBINISM, OCULOCUTANEOUS, TYPE VI" />
      </concept>
      <concept>
        <code value="OMIM:113800" />
        <display value="EPIDERMOLYTIC HYPERKERATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:113900" />
        <display value="PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:113950" />
        <display value="BUNDLE BRANCH BLOCK, FAMILIAL ISOLATED COMPLETE RIGHT" />
      </concept>
      <concept>
        <code value="OMIM:113960" />
        <display value="BUTYRYLESTERASE 1" />
      </concept>
      <concept>
        <code value="OMIM:113970" />
        <display value="BURKITT LYMPHOMA" />
      </concept>
      <concept>
        <code value="OMIM:114000" />
        <display value="CAFFEY DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:114030" />
        <display value="CAFE-AU-LAIT SPOTS, MULTIPLE" />
      </concept>
      <concept>
        <code value="OMIM:114065" />
        <display value="CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:114100" />
        <display value="BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:114140" />
        <display value="CALLOSITIES, HEREDITARY PAINFUL" />
      </concept>
      <concept>
        <code value="OMIM:114150" />
        <display value="CAMPTOBRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:114200" />
        <display value="CAMPTODACTYLY 1" />
      </concept>
      <concept>
        <code value="OMIM:114290" />
        <display value="CAMPOMELIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:114300" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:114450" />
        <display value="CANCER, FAMILIAL, WITH IN VITRO RADIORESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:114480" />
        <display value="BREAST CANCER" />
      </concept>
      <concept>
        <code value="OMIM:114500" />
        <display value="COLORECTAL CANCER" />
      </concept>
      <concept>
        <code value="OMIM:114550" />
        <display value="HEPATOCELLULAR CARCINOMA" />
      </concept>
      <concept>
        <code value="OMIM:114580" />
        <display value="CANDIDIASIS, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:114600" />
        <display value="CANINE TEETH, ABSENCE OF UPPER PERMANENT" />
      </concept>
      <concept>
        <code value="OMIM:114620" />
        <display value="CRANIOFACIOFRONTODIGITAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:114650" />
        <display value="CAR FACTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:114700" />
        <display value="CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH" />
      </concept>
      <concept>
        <code value="OMIM:114900" />
        <display value="CARCINOID TUMORS, INTESTINAL" />
      </concept>
      <concept>
        <code value="OMIM:115000" />
        <display value="CARDIAC ARRHYTHMIA" />
      </concept>
      <concept>
        <code value="OMIM:115080" />
        <display value="CARDIAC CONDUCTION DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:115150" />
        <display value="CARDIOFACIOCUTANEOUS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:115195" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:115196" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:115197" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4" />
      </concept>
      <concept>
        <code value="OMIM:115200" />
        <display value="CARDIOMYOPATHY, DILATED, 1A" />
      </concept>
      <concept>
        <code value="OMIM:115210" />
        <display value="CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:115250" />
        <display value="COLLAGENOMA, FAMILIAL CUTANEOUS" />
      </concept>
      <concept>
        <code value="OMIM:115300" />
        <display value="HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:115310" />
        <display value="PARAGANGLIOMAS 4" />
      </concept>
      <concept>
        <code value="OMIM:115400" />
        <display value="CARPAL DISPLACEMENT" />
      </concept>
      <concept>
        <code value="OMIM:115430" />
        <display value="CARPAL TUNNEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:115470" />
        <display value="CAT EYE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:115645" />
        <display value="CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:115650" />
        <display value="CATARACT 32, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:115660" />
        <display value="CATARACT 7" />
      </concept>
      <concept>
        <code value="OMIM:115665" />
        <display value="CATARACT 8, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:115700" />
        <display value="CATARACT 4, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:115800" />
        <display value="CATARACT 29" />
      </concept>
      <concept>
        <code value="OMIM:115900" />
        <display value="CATARACT 42" />
      </concept>
      <concept>
        <code value="OMIM:116100" />
        <display value="CATARACT 20, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:116200" />
        <display value="CATARACT 1, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:116300" />
        <display value="CATARACT 30, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:116400" />
        <display value="CATARACT 41" />
      </concept>
      <concept>
        <code value="OMIM:116600" />
        <display value="CATARACT 6, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:116700" />
        <display value="CATARACT 13 WITH ADULT i PHENOTYPE" />
      </concept>
      <concept>
        <code value="OMIM:116790" />
        <display value="CATECHOL-O-METHYLTRANSFERASE" />
      </concept>
      <concept>
        <code value="OMIM:116800" />
        <display value="CATARACT 5, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:116850" />
        <display value="CATATRICHY" />
      </concept>
      <concept>
        <code value="OMIM:116860" />
        <display value="CEREBRAL CAVERNOUS MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:116870" />
        <display value="CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENT OF DIAPHRAGM" />
      </concept>
      <concept>
        <code value="OMIM:116920" />
        <display value="LEUKOCYTE ADHESION DEFICIENCY, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:116950" />
        <display value="TEMPERATURE-SENSITIVE AF8 COMPLEMENT" />
      </concept>
      <concept>
        <code value="OMIM:117000" />
        <display value="CENTRAL CORE DISEASE OF MUSCLE" />
      </concept>
      <concept>
        <code value="OMIM:117100" />
        <display value="CENTRALOPATHIC EPILEPSY" />
      </concept>
      <concept>
        <code value="OMIM:117210" />
        <display value="SPINOCEREBELLAR ATAXIA 31" />
      </concept>
      <concept>
        <code value="OMIM:117300" />
        <display value="CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 2" />
      </concept>
      <concept>
        <code value="OMIM:117360" />
        <display value="SPINOCEREBELLAR ATAXIA 29" />
      </concept>
      <concept>
        <code value="OMIM:117550" />
        <display value="SOTOS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:117600" />
        <display value="CEREBRAL SARCOMA" />
      </concept>
      <concept>
        <code value="OMIM:117650" />
        <display value="CEREBROCOSTOMANDIBULAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:117800" />
        <display value="APOCRINE GLAND SECRETION, VARIATION IN" />
      </concept>
      <concept>
        <code value="OMIM:117850" />
        <display value="CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS" />
      </concept>
      <concept>
        <code value="OMIM:117900" />
        <display value="CERVICAL RIB" />
      </concept>
      <concept>
        <code value="OMIM:118000" />
        <display value="CERVICAL VERTEBRAL BRIDGE" />
      </concept>
      <concept>
        <code value="OMIM:118005" />
        <display value="CERVICAL VERTEBRAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:118100" />
        <display value="KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:118200" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B" />
      </concept>
      <concept>
        <code value="OMIM:118210" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1" />
      </concept>
      <concept>
        <code value="OMIM:118220" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A" />
      </concept>
      <concept>
        <code value="OMIM:118230" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:118300" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:118301" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM" />
      </concept>
      <concept>
        <code value="OMIM:118330" />
        <display value="CHEILITIS GLANDULARIS" />
      </concept>
      <concept>
        <code value="OMIM:118350" />
        <display value="CHEMODECTOMA, INTRAABDOMINAL, WITH CUTANEOUS ANGIOLIPOMAS" />
      </concept>
      <concept>
        <code value="OMIM:118400" />
        <display value="CHERUBISM" />
      </concept>
      <concept>
        <code value="OMIM:118420" />
        <display value="CHIARI MALFORMATION TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:118430" />
        <display value="CHLORPROPAMIDE-ALCOHOL FLUSHING" />
      </concept>
      <concept>
        <code value="OMIM:118450" />
        <display value="ALAGILLE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:118600" />
        <display value="CHONDROCALCINOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:118610" />
        <display value="CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION" />
      </concept>
      <concept>
        <code value="OMIM:118650" />
        <display value="CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:118651" />
        <display value="CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:118670" />
        <display value="CHONDRONECTIN" />
      </concept>
      <concept>
        <code value="OMIM:118700" />
        <display value="CHOREA, BENIGN HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:118750" />
        <display value="CHOREOATHETOSIS, FAMILIAL INVERTED" />
      </concept>
      <concept>
        <code value="OMIM:118800" />
        <display value="PAROXYSMAL NONKINESIGENIC DYSKINESIA 1" />
      </concept>
      <concept>
        <code value="OMIM:118830" />
        <display value="CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEIN LIPASE" />
      </concept>
      <concept>
        <code value="OMIM:118840" />
        <display value="CHROMATE RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:118865" />
        <display value="CHOROIDAL OSTEOMA, BILATERAL" />
      </concept>
      <concept>
        <code value="OMIM:118900" />
        <display value="CIRRHOSIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:118943" />
        <display value="CHYMOSIN PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:118980" />
        <display value="CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:119000" />
        <display value="CLEFT CHIN" />
      </concept>
      <concept>
        <code value="OMIM:119100" />
        <display value="SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1" />
      </concept>
      <concept>
        <code value="OMIM:119300" />
        <display value="VAN DER WOUDE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:119500" />
        <display value="POPLITEAL PTERYGIUM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:119530" />
        <display value="OROFACIAL CLEFT 1" />
      </concept>
      <concept>
        <code value="OMIM:119540" />
        <display value="CLEFT PALATE, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:119550" />
        <display value="SYNGNATHIA" />
      </concept>
      <concept>
        <code value="OMIM:119570" />
        <display value="CLEFT SOFT PALATE" />
      </concept>
      <concept>
        <code value="OMIM:119580" />
        <display value="BLEPHAROCHEILODONTIC SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:119600" />
        <display value="CLEIDOCRANIAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:119650" />
        <display value="CLEIDORHIZOMELIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:119800" />
        <display value="CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:119900" />
        <display value="DIGITAL CLUBBING, ISOLATED CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:119915" />
        <display value="CLUSTER HEADACHE, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:120000" />
        <display value="COARCTATION OF AORTA" />
      </concept>
      <concept>
        <code value="OMIM:120040" />
        <display value="COCHLEOSACCULAR DEGENERATION WITH PROGRESSIVE CATARACTS" />
      </concept>
      <concept>
        <code value="OMIM:120050" />
        <display value="COXSACKIEVIRUS B3 SUSCEPTIBILITY" />
      </concept>
      <concept>
        <code value="OMIM:120080" />
        <display value="COLCHICINE RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:120100" />
        <display value="FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:120140" />
        <display value="COLLAGEN, TYPE II, ALPHA-1" />
      </concept>
      <concept>
        <code value="OMIM:120150" />
        <display value="COLLAGEN, TYPE I, ALPHA-1" />
      </concept>
      <concept>
        <code value="OMIM:120200" />
        <display value="COLOBOMA, OCULAR, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:120300" />
        <display value="COLOBOMA OF MACULA" />
      </concept>
      <concept>
        <code value="OMIM:120330" />
        <display value="PAPILLORENAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:120400" />
        <display value="COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:120430" />
        <display value="COLOBOMA OF OPTIC NERVE" />
      </concept>
      <concept>
        <code value="OMIM:120433" />
        <display value="COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:120435" />
        <display value="LYNCH SYNDROME I" />
      </concept>
      <concept>
        <code value="OMIM:120440" />
        <display value="COLONIC VARICES WITHOUT PORTAL HYPERTENSION" />
      </concept>
      <concept>
        <code value="OMIM:120450" />
        <display value="COMEDONES, FAMILIAL DYSKERATOTIC" />
      </concept>
      <concept>
        <code value="OMIM:120500" />
        <display value="COMMISSURAL LIP PITS" />
      </concept>
      <concept>
        <code value="OMIM:120502" />
        <display value="BRANCHIOOTIC SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:120790" />
        <display value="COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:120970" />
        <display value="CONE-ROD DYSTROPHY 2" />
      </concept>
      <concept>
        <code value="OMIM:121050" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 9" />
      </concept>
      <concept>
        <code value="OMIM:121070" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 2E" />
      </concept>
      <concept>
        <code value="OMIM:121200" />
        <display value="SEIZURES, BENIGN FAMILIAL NEONATAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:121201" />
        <display value="SEIZURES, BENIGN FAMILIAL NEONATAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:121210" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:121270" />
        <display value="COPPER DEFICIENCY, FAMILIAL BENIGN" />
      </concept>
      <concept>
        <code value="OMIM:121300" />
        <display value="COPROPORPHYRIA, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:121350" />
        <display value="CORACOCLAVICULAR JOINT, ANOMALOUS" />
      </concept>
      <concept>
        <code value="OMIM:121390" />
        <display value="CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS" />
      </concept>
      <concept>
        <code value="OMIM:121400" />
        <display value="CORNEA PLANA 1, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:121450" />
        <display value="CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:121800" />
        <display value="SCHNYDER CORNEAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:121820" />
        <display value="CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE" />
      </concept>
      <concept>
        <code value="OMIM:121850" />
        <display value="CORNEAL DYSTROPHY, FLECK" />
      </concept>
      <concept>
        <code value="OMIM:121900" />
        <display value="CORNEAL DYSTROPHY, GROENOUW TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:122000" />
        <display value="CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1" />
      </concept>
      <concept>
        <code value="OMIM:122100" />
        <display value="CORNEAL DYSTROPHY, MEESMANN" />
      </concept>
      <concept>
        <code value="OMIM:122200" />
        <display value="CORNEAL DYSTROPHY, LATTICE TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:122400" />
        <display value="EPITHELIAL RECURRENT EROSION DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:122430" />
        <display value="CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS, UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:122440" />
        <display value="CORNEODERMATOOSSEOUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:122450" />
        <display value="CORNEAL HYPESTHESIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:122455" />
        <display value="CORONARY ARTERY DISSECTION, SPONTANEOUS" />
      </concept>
      <concept>
        <code value="OMIM:122460" />
        <display value="HUMAN CORONAVIRUS SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:122470" />
        <display value="CORNELIA DE LANGE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:122550" />
        <display value="CORTICOSTERONE SIDE-CHAIN ISOMERASE" />
      </concept>
      <concept>
        <code value="OMIM:122580" />
        <display value="COSTOCORACOID LIGAMENT, CONGENITALLY SHORT" />
      </concept>
      <concept>
        <code value="OMIM:122600" />
        <display value="SPONDYLOCOSTAL DYSOSTOSIS 5" />
      </concept>
      <concept>
        <code value="OMIM:122700" />
        <display value="COUMARIN RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:122720" />
        <display value="CYTOCHROME P450, SUBFAMILY IIA, POLYPEPTIDE 6" />
      </concept>
      <concept>
        <code value="OMIM:122750" />
        <display value="COXA VARA" />
      </concept>
      <concept>
        <code value="OMIM:122780" />
        <display value="COXOAURICULAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:122850" />
        <display value="CRANIOACROFACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:122860" />
        <display value="CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:122880" />
        <display value="CRANIOFACIAL-DEAFNESS-HAND SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:122900" />
        <display value="CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:123000" />
        <display value="CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:123050" />
        <display value="CRANIORHINY" />
      </concept>
      <concept>
        <code value="OMIM:123100" />
        <display value="CRANIOSYNOSTOSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:123150" />
        <display value="JACKSON-WEISS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:123155" />
        <display value="HYDROCEPHALUS, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:123270" />
        <display value="CREATINE KINASE, BRAIN TYPE, ECTOPIC EXPRESSION OF" />
      </concept>
      <concept>
        <code value="OMIM:123320" />
        <display value="CREATINE PHOSPHOKINASE, ELEVATED SERUM" />
      </concept>
      <concept>
        <code value="OMIM:123400" />
        <display value="CREUTZFELDT-JAKOB DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:123450" />
        <display value="CRI-DU-CHAT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:123500" />
        <display value="CROUZON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:123540" />
        <display value="CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:123550" />
        <display value="CRYOGLOBULINEMIA, FAMILIAL MIXED" />
      </concept>
      <concept>
        <code value="OMIM:123557" />
        <display value="CRYPTOTIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:123560" />
        <display value="CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:123570" />
        <display value="CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:123700" />
        <display value="CUTIS LAXA, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:123790" />
        <display value="BEARE-STEVENSON CUTIS GYRATA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:123853" />
        <display value="CYPRUS FACIAL NEUROMUSCULOSKELETAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:123880" />
        <display value="CYSTIC ANGIOMATOSIS OF BONE, DIFFUSE" />
      </concept>
      <concept>
        <code value="OMIM:123997" />
        <display value="CYTOCHROME c OXIDASE, SUBUNIT 7A2, PSEUDOGENE 2" />
      </concept>
      <concept>
        <code value="OMIM:124000" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:124060" />
        <display value="CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 2" />
      </concept>
      <concept>
        <code value="OMIM:124100" />
        <display value="DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:124200" />
        <display value="DARIER-WHITE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:124300" />
        <display value="DARWINIAN TUBERCLE OF PINNA" />
      </concept>
      <concept>
        <code value="OMIM:124400" />
        <display value="DARWINIAN TUBERCLE OF PINNA" />
      </concept>
      <concept>
        <code value="OMIM:124480" />
        <display value="DEAFNESS, CONGENITAL, WITH ONYCHODYSTROPHY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:124490" />
        <display value="DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY" />
      </concept>
      <concept>
        <code value="OMIM:124500" />
        <display value="VOHWINKEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:124700" />
        <display value="DEAFNESS, MID-TONE NEURAL" />
      </concept>
      <concept>
        <code value="OMIM:124900" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:124950" />
        <display value="DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:125000" />
        <display value="DEAFNESS, UNILATERAL" />
      </concept>
      <concept>
        <code value="OMIM:125050" />
        <display value="DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:125230" />
        <display value="DEAFNESS-CRANIOFACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:125250" />
        <display value="OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:125260" />
        <display value="DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF" />
      </concept>
      <concept>
        <code value="OMIM:125280" />
        <display value="DENS EVAGINATUS" />
      </concept>
      <concept>
        <code value="OMIM:125300" />
        <display value="DENS IN DENTE AND PALATAL INVAGINATIONS" />
      </concept>
      <concept>
        <code value="OMIM:125310" />
        <display value="CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:125320" />
        <display value="DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES" />
      </concept>
      <concept>
        <code value="OMIM:125350" />
        <display value="FAILURE OF TOOTH ERUPTION, PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:125370" />
        <display value="DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:125400" />
        <display value="DENTIN DYSPLASIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:125420" />
        <display value="DENTIN DYSPLASIA, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:125440" />
        <display value="DENTIN DYSPLASIA WITH SCLEROTIC BONES" />
      </concept>
      <concept>
        <code value="OMIM:125460" />
        <display value="DEOXYRIBOSE-5-PHOSPHATE ALDOLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:125480" />
        <display value="MAJOR AFFECTIVE DISORDER 1" />
      </concept>
      <concept>
        <code value="OMIM:125490" />
        <display value="DENTINOGENESIS IMPERFECTA 1" />
      </concept>
      <concept>
        <code value="OMIM:125500" />
        <display value="DENTINOGENESIS IMPERFECTA, SHIELDS TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:125520" />
        <display value="CAYLER CARDIOFACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:125530" />
        <display value="DERMAL RIDGES, NELSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:125540" />
        <display value="DERMAL RIDGES, PATTERNLESS" />
      </concept>
      <concept>
        <code value="OMIM:125550" />
        <display value="DERMAL RIDGES-OFF-THE-END" />
      </concept>
      <concept>
        <code value="OMIM:125570" />
        <display value="DERMATOGLYPHICS--ARCH ON ANY DIGIT" />
      </concept>
      <concept>
        <code value="OMIM:125580" />
        <display value="DERMATOGLYPHICS--FINGER RIDGE COUNT" />
      </concept>
      <concept>
        <code value="OMIM:125590" />
        <display value="DERMATOGLYPHICS--FINGERPRINT PATTERN" />
      </concept>
      <concept>
        <code value="OMIM:125595" />
        <display value="DERMATOPATHIA PIGMENTOSA RETICULARIS" />
      </concept>
      <concept>
        <code value="OMIM:125600" />
        <display value="DERMATOSIS PAPULOSA NIGRA" />
      </concept>
      <concept>
        <code value="OMIM:125630" />
        <display value="VIBRATORY URTICARIA" />
      </concept>
      <concept>
        <code value="OMIM:125635" />
        <display value="DERMOGRAPHISM, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:125640" />
        <display value="DERMOODONTODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:125700" />
        <display value="DIABETES INSIPIDUS, NEUROHYPOPHYSEAL" />
      </concept>
      <concept>
        <code value="OMIM:125800" />
        <display value="DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:125850" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:125851" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:125852" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 2" />
      </concept>
      <concept>
        <code value="OMIM:125853" />
        <display value="DIABETES MELLITUS, NONINSULIN-DEPENDENT" />
      </concept>
      <concept>
        <code value="OMIM:125860" />
        <display value="NAD(P)H DEHYDROGENASE, QUINONE 1" />
      </concept>
      <concept>
        <code value="OMIM:125890" />
        <display value="DIARRHEA, GLUCOSE-STIMULATED SECRETORY, WITH COMMON VARIABLE IMMUNODEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:125900" />
        <display value="DIASTEMA, DENTAL MEDIAL" />
      </concept>
      <concept>
        <code value="OMIM:126050" />
        <display value="DIGITOTALAR DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:126070" />
        <display value="DILUTION, PIGMENTARY" />
      </concept>
      <concept>
        <code value="OMIM:126100" />
        <display value="DIMPLES, FACIAL" />
      </concept>
      <concept>
        <code value="OMIM:126180" />
        <display value="DISCRIMINATION, TWO-POINT, REDUCTION IN" />
      </concept>
      <concept>
        <code value="OMIM:126190" />
        <display value="DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS" />
      </concept>
      <concept>
        <code value="OMIM:126200" />
        <display value="MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:126250" />
        <display value="DISTAL OSTEOSCLEROSIS" />
      </concept>
      <concept>
        <code value="OMIM:126300" />
        <display value="DISTICHIASIS" />
      </concept>
      <concept>
        <code value="OMIM:126320" />
        <display value="DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL VASCULATURE" />
      </concept>
      <concept>
        <code value="OMIM:126370" />
        <display value="DNA, SATELLITE, III" />
      </concept>
      <concept>
        <code value="OMIM:126390" />
        <display value="DNA, LOW-REPETITIVE SEQUENCES OF" />
      </concept>
      <concept>
        <code value="OMIM:126410" />
        <display value="DNA, SATELLITE, ALPHA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:126500" />
        <display value="DOUBLE NAIL FOR FIFTH TOE" />
      </concept>
      <concept>
        <code value="OMIM:126550" />
        <display value="DOUGHNUT LESIONS OF SKULL, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:126600" />
        <display value="DOYNE HONEYCOMB RETINAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:126700" />
        <display value="BASAL LAMINAR DRUSEN" />
      </concept>
      <concept>
        <code value="OMIM:126800" />
        <display value="DUANE RETRACTION SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:126840" />
        <display value="DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:126850" />
        <display value="DUODENAL ULCER, HYPERPEPSINOGENEMIC I" />
      </concept>
      <concept>
        <code value="OMIM:126900" />
        <display value="DUPUYTREN CONTRACTURE" />
      </concept>
      <concept>
        <code value="OMIM:126950" />
        <display value="DWARFISM WITH TALL VERTEBRAE" />
      </concept>
      <concept>
        <code value="OMIM:127000" />
        <display value="KENNY-CAFFEY SYNDROME, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:127100" />
        <display value="DWARFISM, LEVI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:127200" />
        <display value="DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:127300" />
        <display value="LERI-WEILL DYSCHONDROSTEOSIS" />
      </concept>
      <concept>
        <code value="OMIM:127350" />
        <display value="DYSCHONDROSTEOSIS AND NEPHRITIS" />
      </concept>
      <concept>
        <code value="OMIM:127400" />
        <display value="DYSCHROMATOSIS SYMMETRICA HEREDITARIA" />
      </concept>
      <concept>
        <code value="OMIM:127500" />
        <display value="DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1" />
      </concept>
      <concept>
        <code value="OMIM:127550" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:127600" />
        <display value="DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL" />
      </concept>
      <concept>
        <code value="OMIM:127700" />
        <display value="DYSLEXIA, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:127750" />
        <display value="DEMENTIA, LEWY BODY" />
      </concept>
      <concept>
        <code value="OMIM:127800" />
        <display value="DYSPLASIA EPIPHYSEALIS HEMIMELICA" />
      </concept>
      <concept>
        <code value="OMIM:127820" />
        <display value="DYSPLASIA EPIPHYSEALIS HEMIMELICA WITH CHONDROMAS AND OSTEOCHONDROMAS" />
      </concept>
      <concept>
        <code value="OMIM:128000" />
        <display value="DYSTELEPHALANGY" />
      </concept>
      <concept>
        <code value="OMIM:128100" />
        <display value="DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:128101" />
        <display value="DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:128200" />
        <display value="EPISODIC KINESIGENIC DYSKINESIA 1" />
      </concept>
      <concept>
        <code value="OMIM:128230" />
        <display value="DYSTONIA, DOPA-RESPONSIVE" />
      </concept>
      <concept>
        <code value="OMIM:128235" />
        <display value="DYSTONIA 12" />
      </concept>
      <concept>
        <code value="OMIM:128290" />
        <display value="EAR ANTITRAGUS, TAG AT BASE OF" />
      </concept>
      <concept>
        <code value="OMIM:128300" />
        <display value="EAR EXOSTOSES" />
      </concept>
      <concept>
        <code value="OMIM:128400" />
        <display value="EAR FLARE" />
      </concept>
      <concept>
        <code value="OMIM:128500" />
        <display value="EAR FOLDING" />
      </concept>
      <concept>
        <code value="OMIM:128600" />
        <display value="EAR MALFORMATION" />
      </concept>
      <concept>
        <code value="OMIM:128700" />
        <display value="PREAURICULAR FISTULAE, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:128710" />
        <display value="EAR PITS, POSTERIOR HELICAL" />
      </concept>
      <concept>
        <code value="OMIM:128800" />
        <display value="EAR WITHOUT HELIX" />
      </concept>
      <concept>
        <code value="OMIM:128900" />
        <display value="EARLOBE ATTACHMENT, ATTACHED VS UNATTACHED" />
      </concept>
      <concept>
        <code value="OMIM:128950" />
        <display value="EARLOBE CREASE" />
      </concept>
      <concept>
        <code value="OMIM:128980" />
        <display value="EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIAL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:129000" />
        <display value="EARRING HOLES, NATURAL" />
      </concept>
      <concept>
        <code value="OMIM:129100" />
        <display value="EARS, ABILITY TO MOVE" />
      </concept>
      <concept>
        <code value="OMIM:129150" />
        <display value="ECHO VIRUS 11 SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:129200" />
        <display value="BASAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:129400" />
        <display value="RAPP-HODGKIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:129490" />
        <display value="ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:129500" />
        <display value="CLOUSTON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:129510" />
        <display value="ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:129540" />
        <display value="ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE AND PREAXIAL POLYDACTYLY OF FEET" />
      </concept>
      <concept>
        <code value="OMIM:129550" />
        <display value="ECTODERMAL DYSPLASIA WITH ADRENAL CYST" />
      </concept>
      <concept>
        <code value="OMIM:129600" />
        <display value="ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:129750" />
        <display value="ECTOPIA PUPILLAE" />
      </concept>
      <concept>
        <code value="OMIM:129810" />
        <display value="ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE" />
      </concept>
      <concept>
        <code value="OMIM:129830" />
        <display value="ECTRODACTYLY-CLEFT PALATE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:129840" />
        <display value="EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL" />
      </concept>
      <concept>
        <code value="OMIM:129850" />
        <display value="EDINBURGH MALFORMATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:129900" />
        <display value="ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:129905" />
        <display value="EGASYN" />
      </concept>
      <concept>
        <code value="OMIM:130000" />
        <display value="EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1" />
      </concept>
      <concept>
        <code value="OMIM:130010" />
        <display value="EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2" />
      </concept>
      <concept>
        <code value="OMIM:130020" />
        <display value="EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:130050" />
        <display value="EHLERS-DANLOS SYNDROME, VASCULAR TYPE" />
      </concept>
      <concept>
        <code value="OMIM:130060" />
        <display value="EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1" />
      </concept>
      <concept>
        <code value="OMIM:130070" />
        <display value="EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1" />
      </concept>
      <concept>
        <code value="OMIM:130080" />
        <display value="EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1" />
      </concept>
      <concept>
        <code value="OMIM:130090" />
        <display value="EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED" />
      </concept>
      <concept>
        <code value="OMIM:130100" />
        <display value="ELASTOSIS PERFORANS SERPIGINOSA" />
      </concept>
      <concept>
        <code value="OMIM:130180" />
        <display value="ELECTROENCEPHALOGRAM, LOW-VOLTAGE" />
      </concept>
      <concept>
        <code value="OMIM:130190" />
        <display value="ELECTROENCEPHALOGRAPHIC PATTERN, BETA FREQUENCY, QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:130200" />
        <display value="ELECTROENCEPHALOGRAPHIC PECULIARITY: 14 AND 6 PER SEC. POSITIVE SPIKE PHENOMENON" />
      </concept>
      <concept>
        <code value="OMIM:130300" />
        <display value="ELECTROENCEPHALOGRAPHIC PECULIARITY: FRONTO-PRECENTRAL BETA WAVE GROUPS" />
      </concept>
      <concept>
        <code value="OMIM:130400" />
        <display value="ELECTROENCEPHALOGRAPHIC PECULIARITY: OCCIPITAL SLOW BETA WAVES" />
      </concept>
      <concept>
        <code value="OMIM:130600" />
        <display value="ELLIPTOCYTOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:130650" />
        <display value="BECKWITH-WIEDEMANN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:130700" />
        <display value="EMPHYSEMA, HEREDITARY PULMONARY" />
      </concept>
      <concept>
        <code value="OMIM:130710" />
        <display value="EMPHYSEMA, CONGENITAL LOBAR" />
      </concept>
      <concept>
        <code value="OMIM:130720" />
        <display value="LATERAL MENINGOCELE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:130900" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IIIA" />
      </concept>
      <concept>
        <code value="OMIM:130950" />
        <display value="ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD" />
      </concept>
      <concept>
        <code value="OMIM:131100" />
        <display value="MULTIPLE ENDOCRINE NEOPLASIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:131200" />
        <display value="ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:131240" />
        <display value="ENDOTHELIN 1" />
      </concept>
      <concept>
        <code value="OMIM:131300" />
        <display value="CAMURATI-ENGELMANN DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:131375" />
        <display value="ENOLASE, SPERM SPECIFIC" />
      </concept>
      <concept>
        <code value="OMIM:131400" />
        <display value="EOSINOPHILIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:131430" />
        <display value="EOSINOPHILOPENIA" />
      </concept>
      <concept>
        <code value="OMIM:131440" />
        <display value="MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA" />
      </concept>
      <concept>
        <code value="OMIM:131450" />
        <display value="EPIBLEPHARON OF LOWER LID" />
      </concept>
      <concept>
        <code value="OMIM:131460" />
        <display value="EPIBLEPHARON OF UPPER LID" />
      </concept>
      <concept>
        <code value="OMIM:131500" />
        <display value="EPICANTHUS" />
      </concept>
      <concept>
        <code value="OMIM:131600" />
        <display value="EPIDERMOID CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:131705" />
        <display value="TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN" />
      </concept>
      <concept>
        <code value="OMIM:131750" />
        <display value="EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:131760" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:131800" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX, LOCALIZED" />
      </concept>
      <concept>
        <code value="OMIM:131850" />
        <display value="EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL" />
      </concept>
      <concept>
        <code value="OMIM:131880" />
        <display value="EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE" />
      </concept>
      <concept>
        <code value="OMIM:131900" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED" />
      </concept>
      <concept>
        <code value="OMIM:131950" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:131960" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION" />
      </concept>
      <concept>
        <code value="OMIM:132000" />
        <display value="EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS" />
      </concept>
      <concept>
        <code value="OMIM:132090" />
        <display value="EPILEPSY, BENIGN OCCIPITAL" />
      </concept>
      <concept>
        <code value="OMIM:132100" />
        <display value="PHOTOPAROXYSMAL RESPONSE 1" />
      </concept>
      <concept>
        <code value="OMIM:132300" />
        <display value="EPILEPSY, READING" />
      </concept>
      <concept>
        <code value="OMIM:132400" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, 1" />
      </concept>
      <concept>
        <code value="OMIM:132450" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:132500" />
        <display value="EPISTAXIS, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:132600" />
        <display value="PILOMATRIXOMA" />
      </concept>
      <concept>
        <code value="OMIM:132700" />
        <display value="CYLINDROMATOSIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:132800" />
        <display value="MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:132850" />
        <display value="EPSTEIN-BARR VIRUS INSERTION SITE 1" />
      </concept>
      <concept>
        <code value="OMIM:132900" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 4" />
      </concept>
      <concept>
        <code value="OMIM:132990" />
        <display value="ERYTHEMA NODOSUM, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:133000" />
        <display value="ERYTHEMA PALMARE HEREDITARIUM" />
      </concept>
      <concept>
        <code value="OMIM:133020" />
        <display value="ERYTHERMALGIA, PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:133100" />
        <display value="ERYTHROCYTOSIS, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:133180" />
        <display value="ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:133190" />
        <display value="SPINOCEREBELLAR ATAXIA 34" />
      </concept>
      <concept>
        <code value="OMIM:133200" />
        <display value="ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1" />
      </concept>
      <concept>
        <code value="OMIM:133239" />
        <display value="ESOPHAGEAL CANCER" />
      </concept>
      <concept>
        <code value="OMIM:133240" />
        <display value="ESOPHAGEAL RING, LOWER" />
      </concept>
      <concept>
        <code value="OMIM:133260" />
        <display value="ESTERASE B" />
      </concept>
      <concept>
        <code value="OMIM:133270" />
        <display value="ESTERASE C" />
      </concept>
      <concept>
        <code value="OMIM:133300" />
        <display value="ESTERASE ES-2, REGULATOR FOR" />
      </concept>
      <concept>
        <code value="OMIM:133430" />
        <display value="ESTROGEN RECEPTOR 1" />
      </concept>
      <concept>
        <code value="OMIM:133500" />
        <display value="EXCHONDROSIS OF PINNA, POSTERIOR" />
      </concept>
      <concept>
        <code value="OMIM:133540" />
        <display value="COCKAYNE SYNDROME B" />
      </concept>
      <concept>
        <code value="OMIM:133600" />
        <display value="EXOSTOSES OF HEEL" />
      </concept>
      <concept>
        <code value="OMIM:133690" />
        <display value="EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E" />
      </concept>
      <concept>
        <code value="OMIM:133700" />
        <display value="EXOSTOSES, MULTIPLE, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:133701" />
        <display value="EXOSTOSES, MULTIPLE, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:133705" />
        <display value="EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS" />
      </concept>
      <concept>
        <code value="OMIM:133750" />
        <display value="EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATION AND MICROCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:133780" />
        <display value="EXUDATIVE VITREORETINOPATHY 1" />
      </concept>
      <concept>
        <code value="OMIM:133800" />
        <display value="EYEBROW, WHORL IN" />
      </concept>
      <concept>
        <code value="OMIM:133900" />
        <display value="HEMIFACIAL HYPERPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:134000" />
        <display value="FACIAL HYPERTRICHOSIS" />
      </concept>
      <concept>
        <code value="OMIM:134200" />
        <display value="FACIAL PALSY, FAMILIAL RECURRENT PERIPHERAL" />
      </concept>
      <concept>
        <code value="OMIM:134300" />
        <display value="FACIAL SPASM" />
      </concept>
      <concept>
        <code value="OMIM:134400" />
        <display value="FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS" />
      </concept>
      <concept>
        <code value="OMIM:134430" />
        <display value="FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:134500" />
        <display value="FACTOR VIII DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:134510" />
        <display value="FACTOR VIII AND FACTOR IX, COMBINED DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:134520" />
        <display value="FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:134540" />
        <display value="FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:134600" />
        <display value="FANCONI RENOTUBULAR SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:134610" />
        <display value="FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:134720" />
        <display value="FECUNDITY GENE, BOOROOLA, OF SHEEP, HOMOLOG OF" />
      </concept>
      <concept>
        <code value="OMIM:134750" />
        <display value="FELTY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:134780" />
        <display value="FEMORAL-FACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:134900" />
        <display value="FIBRINOLYTIC DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:135100" />
        <display value="FIBRODYSPLASIA OSSIFICANS PROGRESSIVA" />
      </concept>
      <concept>
        <code value="OMIM:135150" />
        <display value="BIRT-HOGG-DUBE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:135290" />
        <display value="DESMOID DISEASE, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:135300" />
        <display value="FIBROMATOSIS, GINGIVAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:135400" />
        <display value="HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:135500" />
        <display value="ZIMMERMANN-LABAND SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:135550" />
        <display value="FIBROMATOSIS, GINGIVAL, WITH PROGRESSIVE DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:135580" />
        <display value="FIBROMUSCULAR DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:135610" />
        <display value="FIBRONECTIN-LIKE 2" />
      </concept>
      <concept>
        <code value="OMIM:135700" />
        <display value="FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:135750" />
        <display value="LAURIN-SANDROW SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:135800" />
        <display value="FIBULA, RECURRENT DISLOCATION OF HEAD OF" />
      </concept>
      <concept>
        <code value="OMIM:135900" />
        <display value="COFFIN-SIRIS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:135950" />
        <display value="FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION AND PROPORTIONATE SHORT STATURE" />
      </concept>
      <concept>
        <code value="OMIM:136000" />
        <display value="ADERMATOGLYPHIA" />
      </concept>
      <concept>
        <code value="OMIM:136100" />
        <display value="FINGERS, RELATIVE LENGTH OF" />
      </concept>
      <concept>
        <code value="OMIM:136120" />
        <display value="FISH-EYE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:136140" />
        <display value="FLOATING-HARBOR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:136150" />
        <display value="FLOOD FACTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:136200" />
        <display value="FLUSHING OF EARS AND SOMNOLENCE" />
      </concept>
      <concept>
        <code value="OMIM:136300" />
        <display value="FLYNN-AIRD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:136400" />
        <display value="FOCAL EPITHELIAL HYPERPLASIA OF THE ORAL MUCOSA" />
      </concept>
      <concept>
        <code value="OMIM:136480" />
        <display value="FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:136500" />
        <display value="FOCAL FACIAL DERMAL DYSPLASIA 1, BRAUER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:136520" />
        <display value="FOVEAL HYPOPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:136540" />
        <display value="FRAGILE SITE 10q23" />
      </concept>
      <concept>
        <code value="OMIM:136550" />
        <display value="MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:136570" />
        <display value="CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KB" />
      </concept>
      <concept>
        <code value="OMIM:136580" />
        <display value="FRAGILE SITE, DISTAMYCIN A TYPE, RARE, FRA(16)(q22.1)" />
      </concept>
      <concept>
        <code value="OMIM:136590" />
        <display value="FRAGILE SITE 20p11" />
      </concept>
      <concept>
        <code value="OMIM:136600" />
        <display value="FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURAL DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:136620" />
        <display value="FRAGILE SITE 10q25" />
      </concept>
      <concept>
        <code value="OMIM:136630" />
        <display value="MENTAL RETARDATION, FRA12A TYPE" />
      </concept>
      <concept>
        <code value="OMIM:136640" />
        <display value="FRAGILE SITE 9q32" />
      </concept>
      <concept>
        <code value="OMIM:136660" />
        <display value="FRAGILE SITE 17p12" />
      </concept>
      <concept>
        <code value="OMIM:136680" />
        <display value="FRASIER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:136760" />
        <display value="FRONTONASAL DYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:136800" />
        <display value="CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:136830" />
        <display value="FUCOSIDASE REGULATOR" />
      </concept>
      <concept>
        <code value="OMIM:136880" />
        <display value="FUNDUS ALBIPUNCTATUS" />
      </concept>
      <concept>
        <code value="OMIM:136900" />
        <display value="SORSBY FUNDUS DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:137000" />
        <display value="FUTCHER LINE" />
      </concept>
      <concept>
        <code value="OMIM:137040" />
        <display value="GALLBLADDER, AGENESIS OF" />
      </concept>
      <concept>
        <code value="OMIM:137050" />
        <display value="GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF" />
      </concept>
      <concept>
        <code value="OMIM:137100" />
        <display value="IMMUNOGLOBULIN A DEFICIENCY 1" />
      </concept>
      <concept>
        <code value="OMIM:137130" />
        <display value="GASTRIC SNEEZING" />
      </concept>
      <concept>
        <code value="OMIM:137200" />
        <display value="NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:137210" />
        <display value="GASTRIC VOLVULUS, INTRATHORACIC" />
      </concept>
      <concept>
        <code value="OMIM:137215" />
        <display value="GASTRIC CANCER, HEREDITARY DIFFUSE" />
      </concept>
      <concept>
        <code value="OMIM:137220" />
        <display value="GASTRIC JUICE PEPTIDES" />
      </concept>
      <concept>
        <code value="OMIM:137241" />
        <display value="GASTRIC INHIBITORY POLYPEPTIDE RECEPTOR" />
      </concept>
      <concept>
        <code value="OMIM:137245" />
        <display value="LYMPHOMA, MUCOSA-ASSOCIATED LYMPHOID TYPE" />
      </concept>
      <concept>
        <code value="OMIM:137270" />
        <display value="GASTROCUTANEOUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:137280" />
        <display value="GASTRITIS, FAMILIAL GIANT HYPERTROPHIC" />
      </concept>
      <concept>
        <code value="OMIM:137360" />
        <display value="GENOCHONDROMATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:137370" />
        <display value="GENU VALGUM, ST. HELENA FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:137400" />
        <display value="GEOGRAPHIC AND FISSURED TONGUE" />
      </concept>
      <concept>
        <code value="OMIM:137440" />
        <display value="GERSTMANN-STRAUSSLER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:137500" />
        <display value="GIANT NEUTROPHIL LEUKOCYTES" />
      </concept>
      <concept>
        <code value="OMIM:137550" />
        <display value="MELANOCYTIC NEVUS SYNDROME, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:137575" />
        <display value="GIGANTIFORM CEMENTOMA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:137580" />
        <display value="GILLES DE LA TOURETTE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:137600" />
        <display value="ANTERIOR SEGMENT DYSGENESIS 4" />
      </concept>
      <concept>
        <code value="OMIM:137700" />
        <display value="GLAUCOMA WITH ELEVATED EPISCLERAL VENOUS PRESSURE" />
      </concept>
      <concept>
        <code value="OMIM:137750" />
        <display value="GLAUCOMA 1, OPEN ANGLE, A" />
      </concept>
      <concept>
        <code value="OMIM:137760" />
        <display value="GLAUCOMA, PRIMARY OPEN ANGLE" />
      </concept>
      <concept>
        <code value="OMIM:137763" />
        <display value="GLAUCOMA AND SLEEP APNEA" />
      </concept>
      <concept>
        <code value="OMIM:137800" />
        <display value="GLIOMA SUSCEPTIBILITY 1" />
      </concept>
      <concept>
        <code value="OMIM:137900" />
        <display value="GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN" />
      </concept>
      <concept>
        <code value="OMIM:137920" />
        <display value="RENAL CYSTS AND DIABETES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:137940" />
        <display value="HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:137950" />
        <display value="GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1" />
      </concept>
      <concept>
        <code value="OMIM:138000" />
        <display value="GLOMUVENOUS MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:138060" />
        <display value="GLUCOCORTICOID RECEPTOR-LIKE 1" />
      </concept>
      <concept>
        <code value="OMIM:138070" />
        <display value="GLUCOGLYCINURIA" />
      </concept>
      <concept>
        <code value="OMIM:138110" />
        <display value="GLUCOSE-6-PHOSPHATE DEHYDROGENASE-LIKE" />
      </concept>
      <concept>
        <code value="OMIM:138277" />
        <display value="GLUTAMIC ACID DECARBOXYLASE, BRAIN, MEMBRANE FORM" />
      </concept>
      <concept>
        <code value="OMIM:138300" />
        <display value="GLUTATHIONE REDUCTASE" />
      </concept>
      <concept>
        <code value="OMIM:138340" />
        <display value="GLUTATHIONE TRANSFERASE ACTIVITY TOWARD TRANS-STILBENE OXIDE" />
      </concept>
      <concept>
        <code value="OMIM:138500" />
        <display value="HYPERGLYCINURIA" />
      </concept>
      <concept>
        <code value="OMIM:138710" />
        <display value="GLYCOPROTEIN, RENAL" />
      </concept>
      <concept>
        <code value="OMIM:138770" />
        <display value="GMS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:138790" />
        <display value="GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:138800" />
        <display value="GOITER, MULTINODULAR 1, WITH OR WITHOUT SERTOLI-LEYDIG CELL TUMORS" />
      </concept>
      <concept>
        <code value="OMIM:138900" />
        <display value="URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:138920" />
        <display value="GRANDDAD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:138930" />
        <display value="GRANT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:138990" />
        <display value="GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL DOMINANT TYPE" />
      </concept>
      <concept>
        <code value="OMIM:139000" />
        <display value="GRANULOSIS RUBRA NASI" />
      </concept>
      <concept>
        <code value="OMIM:139090" />
        <display value="GRAY PLATELET SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:139100" />
        <display value="GRAYING OF HAIR, PRECOCIOUS" />
      </concept>
      <concept>
        <code value="OMIM:139210" />
        <display value="MYHRE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:139280" />
        <display value="GUANYLATE KINASE 2" />
      </concept>
      <concept>
        <code value="OMIM:139290" />
        <display value="GUANYLATE KINASE 3" />
      </concept>
      <concept>
        <code value="OMIM:139300" />
        <display value="AROMATASE EXCESS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:139393" />
        <display value="GUILLAIN-BARRE SYNDROME, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:139400" />
        <display value="HAIR WHORL" />
      </concept>
      <concept>
        <code value="OMIM:139450" />
        <display value="HAIR MORPHOLOGY 2" />
      </concept>
      <concept>
        <code value="OMIM:139500" />
        <display value="HAIRY EARS" />
      </concept>
      <concept>
        <code value="OMIM:139600" />
        <display value="HAIRY ELBOWS" />
      </concept>
      <concept>
        <code value="OMIM:139630" />
        <display value="HAIRY NOSE TIP" />
      </concept>
      <concept>
        <code value="OMIM:139650" />
        <display value="HAIRY PALMS AND SOLES" />
      </concept>
      <concept>
        <code value="OMIM:139750" />
        <display value="HAND AND FOOT DEFORMITY WITH FLAT FACIES" />
      </concept>
      <concept>
        <code value="OMIM:139800" />
        <display value="HAND CLASPING PATTERN" />
      </concept>
      <concept>
        <code value="OMIM:139900" />
        <display value="HAND SKILL, RELATIVE" />
      </concept>
      <concept>
        <code value="OMIM:140000" />
        <display value="HAND-FOOT-GENITAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:140300" />
        <display value="HASHIMOTO THYROIDITIS" />
      </concept>
      <concept>
        <code value="OMIM:140350" />
        <display value="HAWKINSINURIA" />
      </concept>
      <concept>
        <code value="OMIM:140400" />
        <display value="PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:140450" />
        <display value="HEART-HAND SYNDROME, SPANISH TYPE" />
      </concept>
      <concept>
        <code value="OMIM:140500" />
        <display value="HEART, MALFORMATION OF" />
      </concept>
      <concept>
        <code value="OMIM:140600" />
        <display value="OSTEOARTHRITIS SUSCEPTIBILITY 2" />
      </concept>
      <concept>
        <code value="OMIM:140700" />
        <display value="HEINZ BODY ANEMIAS" />
      </concept>
      <concept>
        <code value="OMIM:140850" />
        <display value="HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE" />
      </concept>
      <concept>
        <code value="OMIM:140900" />
        <display value="HEMANGIOMAS OF SMALL INTESTINE" />
      </concept>
      <concept>
        <code value="OMIM:141000" />
        <display value="HEMANGIOMA-THROMBOCYTOPENIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:141200" />
        <display value="HEMATURIA, BENIGN FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:141300" />
        <display value="HEMIFACIAL ATROPHY, PROGRESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:141350" />
        <display value="HEMIFACIAL HYPERPLASIA WITH STRABISMUS" />
      </concept>
      <concept>
        <code value="OMIM:141400" />
        <display value="HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:141405" />
        <display value="HEMIFACIAL SPASM, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:141500" />
        <display value="MIGRAINE, FAMILIAL HEMIPLEGIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:141700" />
        <display value="HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES" />
      </concept>
      <concept>
        <code value="OMIM:141749" />
        <display value="FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:141750" />
        <display value="ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:142309" />
        <display value="HEMOGLOBIN--VARIANTS FOR WHICH THE CHAIN CARRYING THE MUTATION IS UNKNOWN OR UNCERTAIN" />
      </concept>
      <concept>
        <code value="OMIM:142330" />
        <display value="HEPATIC ADENOMAS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:142335" />
        <display value="FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:142340" />
        <display value="DIAPHRAGMATIC HERNIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:142350" />
        <display value="HERNIA, DOUBLE INGUINAL" />
      </concept>
      <concept>
        <code value="OMIM:142395" />
        <display value="HEPATITIS B VACCINE, RESPONSE TO" />
      </concept>
      <concept>
        <code value="OMIM:142400" />
        <display value="HERNIA, HIATUS" />
      </concept>
      <concept>
        <code value="OMIM:142470" />
        <display value="FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:142500" />
        <display value="HETEROCHROMIA IRIDIS" />
      </concept>
      <concept>
        <code value="OMIM:142623" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:142625" />
        <display value="HIRSUTISM, SKELETAL DYSPLASIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:142630" />
        <display value="HISTIOCYTOSIS, PROGRESSIVE MUCINOUS" />
      </concept>
      <concept>
        <code value="OMIM:142660" />
        <display value="HEXOSAMINIDASE C" />
      </concept>
      <concept>
        <code value="OMIM:142669" />
        <display value="BEUKES HIP DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:142680" />
        <display value="PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:142690" />
        <display value="ACNE INVERSA, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:142700" />
        <display value="DEVELOPMENTAL DYSPLASIA OF THE HIP 1" />
      </concept>
      <concept>
        <code value="OMIM:142730" />
        <display value="HISTIOCYTIC DERMATOARTHRITIS" />
      </concept>
      <concept>
        <code value="OMIM:142770" />
        <display value="HLA MODIFIER" />
      </concept>
      <concept>
        <code value="OMIM:142830" />
        <display value="MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, B" />
      </concept>
      <concept>
        <code value="OMIM:142900" />
        <display value="HOLT-ORAM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:142910" />
        <display value="3-HYDROXY-3-METHYLGLUTARYL-CoA REDUCTASE" />
      </concept>
      <concept>
        <code value="OMIM:142945" />
        <display value="HOLOPROSENCEPHALY 3" />
      </concept>
      <concept>
        <code value="OMIM:142946" />
        <display value="HOLOPROSENCEPHALY 4" />
      </concept>
      <concept>
        <code value="OMIM:143000" />
        <display value="HORNER SYNDROME, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:143020" />
        <display value="HPA I RECOGNITION POLYMORPHISM, BETA-GLOBIN-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:143050" />
        <display value="HUMERORADIAL SYNOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:143095" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS" />
      </concept>
      <concept>
        <code value="OMIM:143100" />
        <display value="HUNTINGTON DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:143200" />
        <display value="WAGNER VITREORETINOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:143400" />
        <display value="CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2" />
      </concept>
      <concept>
        <code value="OMIM:143460" />
        <display value="5-HYDROXYTRYPTAMINE OXYGENASE REGULATOR" />
      </concept>
      <concept>
        <code value="OMIM:143465" />
        <display value="ATTENTION DEFICIT-HYPERACTIVITY DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:143470" />
        <display value="HYPERALPHALIPOPROTEINEMIA 1" />
      </concept>
      <concept>
        <code value="OMIM:143500" />
        <display value="GILBERT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:143850" />
        <display value="ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:143860" />
        <display value="HYPERCHLORHIDROSIS, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:143870" />
        <display value="HYPERCALCIURIA, ABSORPTIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:143880" />
        <display value="HYPERCALCEMIA, INFANTILE, 1" />
      </concept>
      <concept>
        <code value="OMIM:143890" />
        <display value="HYPERCHOLESTEROLEMIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:144010" />
        <display value="HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B" />
      </concept>
      <concept>
        <code value="OMIM:144020" />
        <display value="HYPERCHOLESTEROLEMIA SUPPRESSOR" />
      </concept>
      <concept>
        <code value="OMIM:144050" />
        <display value="HYPERHEPARINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:144100" />
        <display value="HYPERHIDROSIS, GUSTATORY" />
      </concept>
      <concept>
        <code value="OMIM:144110" />
        <display value="HYPERHIDROSIS PALMARIS ET PLANTARIS" />
      </concept>
      <concept>
        <code value="OMIM:144120" />
        <display value="HYPERIMMUNOGLOBULIN G1(A1) SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:144150" />
        <display value="HYPERKERATOSIS LENTICULARIS PERSTANS" />
      </concept>
      <concept>
        <code value="OMIM:144190" />
        <display value="HYPERKERATOSIS-HYPERPIGMENTATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:144200" />
        <display value="PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC" />
      </concept>
      <concept>
        <code value="OMIM:144250" />
        <display value="HYPERLIPIDEMIA, FAMILIAL COMBINED" />
      </concept>
      <concept>
        <code value="OMIM:144300" />
        <display value="HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:144600" />
        <display value="HYPERLIPOPROTEINEMIA, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:144650" />
        <display value="HYPERLIPOPROTEINEMIA, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:144700" />
        <display value="RENAL CELL CARCINOMA, NONPAPILLARY" />
      </concept>
      <concept>
        <code value="OMIM:144750" />
        <display value="ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:144755" />
        <display value="HYPEROSTOSIS CRANIALIS INTERNA" />
      </concept>
      <concept>
        <code value="OMIM:144800" />
        <display value="HYPEROSTOSIS FRONTALIS INTERNA" />
      </concept>
      <concept>
        <code value="OMIM:145000" />
        <display value="HYPERPARATHYROIDISM 1" />
      </concept>
      <concept>
        <code value="OMIM:145001" />
        <display value="HYPERPARATHYROIDISM 2 WITH JAW TUMORS" />
      </concept>
      <concept>
        <code value="OMIM:145100" />
        <display value="HYPERPIGMENTATION OF EYELIDS" />
      </concept>
      <concept>
        <code value="OMIM:145200" />
        <display value="HYPERPIGMENTATION OF FULDAUER AND KUIJPERS" />
      </concept>
      <concept>
        <code value="OMIM:145250" />
        <display value="HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:145260" />
        <display value="PSEUDOHYPOALDOSTERONISM, TYPE IIA" />
      </concept>
      <concept>
        <code value="OMIM:145270" />
        <display value="HYPERPROGLUCAGONEMIA" />
      </concept>
      <concept>
        <code value="OMIM:145290" />
        <display value="HYPERREFLEXIA" />
      </concept>
      <concept>
        <code value="OMIM:145295" />
        <display value="HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:145300" />
        <display value="HYPERSENSITIVITY PNEUMONITIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:145350" />
        <display value="HYPERTAURINURIC CARDIOMYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:145400" />
        <display value="HYPERTELORISM" />
      </concept>
      <concept>
        <code value="OMIM:145410" />
        <display value="OPITZ GBBB SYNDROME, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:145420" />
        <display value="HYPERTELORISM, TEEBI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:145500" />
        <display value="HYPERTENSION, ESSENTIAL" />
      </concept>
      <concept>
        <code value="OMIM:145590" />
        <display value="HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA" />
      </concept>
      <concept>
        <code value="OMIM:145600" />
        <display value="MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:145650" />
        <display value="THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY" />
      </concept>
      <concept>
        <code value="OMIM:145680" />
        <display value="HYPERTHYROXINEMIA, DYSTRANSTHYRETINEMIC" />
      </concept>
      <concept>
        <code value="OMIM:145700" />
        <display value="HYPERTRICHOSIS LANUGINOSA CONGENITA" />
      </concept>
      <concept>
        <code value="OMIM:145701" />
        <display value="HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:145750" />
        <display value="HYPERTRIGLYCERIDEMIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:145800" />
        <display value="HYPERTROPHIA MUSCULORUM VERA" />
      </concept>
      <concept>
        <code value="OMIM:145900" />
        <display value="HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS" />
      </concept>
      <concept>
        <code value="OMIM:145980" />
        <display value="HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:145981" />
        <display value="HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:146000" />
        <display value="HYPOCHONDROPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:146110" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:146160" />
        <display value="HYPOMELIA WITH MULLERIAN DUCT ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:146200" />
        <display value="HYPOPARATHYROIDISM, FAMILIAL ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:146255" />
        <display value="HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:146300" />
        <display value="HYPOPHOSPHATASIA, ADULT" />
      </concept>
      <concept>
        <code value="OMIM:146350" />
        <display value="HYPOPHOSPHATEMIC BONE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:146390" />
        <display value="CHROMOSOME 18p DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:146450" />
        <display value="HYPOSPADIAS 3, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:146500" />
        <display value="MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:146510" />
        <display value="PALLISTER-HALL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:146520" />
        <display value="HYPOTRICHOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:146550" />
        <display value="HYPOTRICHOSIS 4" />
      </concept>
      <concept>
        <code value="OMIM:146580" />
        <display value="HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE SUPPRESSOR" />
      </concept>
      <concept>
        <code value="OMIM:146590" />
        <display value="ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:146600" />
        <display value="ICHTHYOSIS HYSTRIX GRAVIOR" />
      </concept>
      <concept>
        <code value="OMIM:146700" />
        <display value="ICHTHYOSIS VULGARIS" />
      </concept>
      <concept>
        <code value="OMIM:146720" />
        <display value="ICHTHYOSIS--CHEEK--EYEBROW SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:146750" />
        <display value="ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:146800" />
        <display value="ICHTHYOSIS BULLOSA OF SIEMENS" />
      </concept>
      <concept>
        <code value="OMIM:146810" />
        <display value="IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRPHEGAL" />
      </concept>
      <concept>
        <code value="OMIM:146820" />
        <display value="IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGAT" />
      </concept>
      <concept>
        <code value="OMIM:146830" />
        <display value="IMMUNE DEFICIENCY, FAMILIAL VARIABLE" />
      </concept>
      <concept>
        <code value="OMIM:146840" />
        <display value="IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST" />
      </concept>
      <concept>
        <code value="OMIM:146850" />
        <display value="IMMUNE SUPPRESSION" />
      </concept>
      <concept>
        <code value="OMIM:146950" />
        <display value="IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRHGAL" />
      </concept>
      <concept>
        <code value="OMIM:146960" />
        <display value="IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRTGAL" />
      </concept>
      <concept>
        <code value="OMIM:146990" />
        <display value="IMMUNOGLOBULIN HEAVY CHAIN DIVERSITY REGION 2" />
      </concept>
      <concept>
        <code value="OMIM:147050" />
        <display value="IgE RESPONSIVENESS, ATOPIC" />
      </concept>
      <concept>
        <code value="OMIM:147060" />
        <display value="HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:147061" />
        <display value="IMMUNOGLOBULIN E CONCENTRATION, SERUM" />
      </concept>
      <concept>
        <code value="OMIM:147080" />
        <display value="IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGLPHE 1" />
      </concept>
      <concept>
        <code value="OMIM:147090" />
        <display value="IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGLPHE 2" />
      </concept>
      <concept>
        <code value="OMIM:147250" />
        <display value="SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR" />
      </concept>
      <concept>
        <code value="OMIM:147251" />
        <display value="INCISORS, FUSED MANDIBULAR" />
      </concept>
      <concept>
        <code value="OMIM:147260" />
        <display value="IMMUNOGLOBULIN SWITCH SEQUENCES" />
      </concept>
      <concept>
        <code value="OMIM:147300" />
        <display value="INCISORS, LONG UPPER CENTRAL" />
      </concept>
      <concept>
        <code value="OMIM:147320" />
        <display value="INSULIN RECEPTORS, FAMILIAL INCREASE IN" />
      </concept>
      <concept>
        <code value="OMIM:147330" />
        <display value="INCISORS, LOWER CENTRAL, ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:147350" />
        <display value="INCISORS, ROTATION OF UPPER CENTRAL" />
      </concept>
      <concept>
        <code value="OMIM:147400" />
        <display value="INCISORS, SHOVEL-SHAPED" />
      </concept>
      <concept>
        <code value="OMIM:147421" />
        <display value="INCLUSION BODY MYOSITIS" />
      </concept>
      <concept>
        <code value="OMIM:147430" />
        <display value="MARSILI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:147480" />
        <display value="CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1" />
      </concept>
      <concept>
        <code value="OMIM:147530" />
        <display value="INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:147540" />
        <display value="INSECT STINGS, HYPERSENSITIVITY TO" />
      </concept>
      <concept>
        <code value="OMIM:147545" />
        <display value="INSULIN RECEPTOR SUBSTRATE 1" />
      </concept>
      <concept>
        <code value="OMIM:147560" />
        <display value="INTERFERON ANTIVIRAL DEPRESSOR" />
      </concept>
      <concept>
        <code value="OMIM:147610" />
        <display value="IRIS PIGMENT LAYER, CLEAVAGE OF" />
      </concept>
      <concept>
        <code value="OMIM:147630" />
        <display value="INSULINOMATOSIS AND DIABETES MELLITUS" />
      </concept>
      <concept>
        <code value="OMIM:147710" />
        <display value="INTUSSUSCEPTION" />
      </concept>
      <concept>
        <code value="OMIM:147750" />
        <display value="IVIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:147770" />
        <display value="JOHNSON NEUROECTODERMAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:147791" />
        <display value="JACOBSEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:147800" />
        <display value="AASE-SMITH SYNDROME I" />
      </concept>
      <concept>
        <code value="OMIM:147820" />
        <display value="INTERNAL CAROTID ARTERY, SPONTANEOUS DISSECTION OF" />
      </concept>
      <concept>
        <code value="OMIM:147860" />
        <display value="INTERFERON, BETA-3" />
      </concept>
      <concept>
        <code value="OMIM:147891" />
        <display value="ISCHIOCOXOPODOPATELLAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:147900" />
        <display value="JOINT LAXITY, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:147920" />
        <display value="KABUKI SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:147950" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:148000" />
        <display value="KAPOSI SARCOMA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:148050" />
        <display value="KBG SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:148100" />
        <display value="KELOID FORMATION" />
      </concept>
      <concept>
        <code value="OMIM:148190" />
        <display value="KERATITIS, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:148200" />
        <display value="KERATOENDOTHELIITIS FUGAX HEREDITARIA" />
      </concept>
      <concept>
        <code value="OMIM:148210" />
        <display value="KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:148300" />
        <display value="KERATOCONUS 1" />
      </concept>
      <concept>
        <code value="OMIM:148350" />
        <display value="KERATODERMA, PALMOPLANTAR, WITH DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:148360" />
        <display value="KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORY NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:148370" />
        <display value="KERATOLYTIC WINTER ERYTHEMA" />
      </concept>
      <concept>
        <code value="OMIM:148390" />
        <display value="KERATOSIS, FAMILIAL ACTINIC" />
      </concept>
      <concept>
        <code value="OMIM:148500" />
        <display value="TYLOSIS WITH ESOPHAGEAL CANCER" />
      </concept>
      <concept>
        <code value="OMIM:148520" />
        <display value="KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:148600" />
        <display value="PALMOPLANTAR KERATODERMA, PUNCTATE TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:148700" />
        <display value="PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE" />
      </concept>
      <concept>
        <code value="OMIM:148730" />
        <display value="KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL" />
      </concept>
      <concept>
        <code value="OMIM:148800" />
        <display value="KLEEBLATTSCHAEDEL" />
      </concept>
      <concept>
        <code value="OMIM:148820" />
        <display value="WAARDENBURG SYNDROME, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:148840" />
        <display value="KLEINE-LEVIN HIBERNATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:149000" />
        <display value="KLIPPEL-TRENAUNAY-WEBER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:149100" />
        <display value="KNUCKLE PADS" />
      </concept>
      <concept>
        <code value="OMIM:149200" />
        <display value="KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:149300" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:149400" />
        <display value="HYPEREKPLEXIA 1" />
      </concept>
      <concept>
        <code value="OMIM:149500" />
        <display value="KYRLE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:149600" />
        <display value="LABIA MINORA, INCOMPLETE ADHESION OF" />
      </concept>
      <concept>
        <code value="OMIM:149700" />
        <display value="LACRIMAL DUCT DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:149730" />
        <display value="LACRIMOAURICULODENTODIGITAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:150170" />
        <display value="LACTIC ACIDOSIS, CHRONIC ADULT FORM" />
      </concept>
      <concept>
        <code value="OMIM:150230" />
        <display value="TRICHORHINOPHALANGEAL SYNDROME, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:150250" />
        <display value="LARSEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:150260" />
        <display value="LARYNGEAL ABDUCTOR PARALYSIS" />
      </concept>
      <concept>
        <code value="OMIM:150270" />
        <display value="LARYNGEAL ADDUCTOR PARALYSIS" />
      </concept>
      <concept>
        <code value="OMIM:150280" />
        <display value="LARYNGOMALACIA" />
      </concept>
      <concept>
        <code value="OMIM:150300" />
        <display value="LARYNX, CONGENITAL PARTIAL ATRESIA OF" />
      </concept>
      <concept>
        <code value="OMIM:150360" />
        <display value="LARYNGEAL WEB, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:150400" />
        <display value="TOOTH AGENESIS, SELECTIVE, 4" />
      </concept>
      <concept>
        <code value="OMIM:150500" />
        <display value="LATTICE DEGENERATION OF RETINA LEADING TO RETINAL DETACHMENT" />
      </concept>
      <concept>
        <code value="OMIM:150550" />
        <display value="LAZY LEUKOCYTE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:150590" />
        <display value="LEG ULCERS, FAMILIAL, OF JUVENILE ONSET" />
      </concept>
      <concept>
        <code value="OMIM:150600" />
        <display value="LEGG-CALVE-PERTHES DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:150699" />
        <display value="LEIOMYOMA, UTERINE" />
      </concept>
      <concept>
        <code value="OMIM:150700" />
        <display value="LEIOMYOMA OF VULVA AND ESOPHAGUS" />
      </concept>
      <concept>
        <code value="OMIM:150800" />
        <display value="HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER" />
      </concept>
      <concept>
        <code value="OMIM:150900" />
        <display value="LENTIGINES" />
      </concept>
      <concept>
        <code value="OMIM:151000" />
        <display value="LENTIGINOSIS, CENTROFACIAL NEURODYSRAPHIC" />
      </concept>
      <concept>
        <code value="OMIM:151001" />
        <display value="LENTIGINOSIS, INHERITED PATTERNED" />
      </concept>
      <concept>
        <code value="OMIM:151050" />
        <display value="LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM" />
      </concept>
      <concept>
        <code value="OMIM:151100" />
        <display value="LEOPARD SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:151200" />
        <display value="CHROMOSOME 8q22.1 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:151210" />
        <display value="PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:151380" />
        <display value="LEUKEMIA, ACUTE MONOCYTIC" />
      </concept>
      <concept>
        <code value="OMIM:151400" />
        <display value="LEUKEMIA, CHRONIC LYMPHOCYTIC" />
      </concept>
      <concept>
        <code value="OMIM:151430" />
        <display value="B-CELL CLL/LYMPHOMA 2" />
      </concept>
      <concept>
        <code value="OMIM:151450" />
        <display value="LEUKOCYTE ANTIGEN GROUP FIVE" />
      </concept>
      <concept>
        <code value="OMIM:151500" />
        <display value="LEUKOCYTE NUCLEAR APPENDAGES, HEREDITARY PREVALENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:151590" />
        <display value="LICHEN SCLEROSUS ET ATROPHICUS" />
      </concept>
      <concept>
        <code value="OMIM:151600" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:151610" />
        <display value="LEVATOR-MEDIAL RECTUS SYNKINESIS" />
      </concept>
      <concept>
        <code value="OMIM:151620" />
        <display value="LICHEN PLANUS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:151623" />
        <display value="LI-FRAUMENI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:151630" />
        <display value="LIP, MEDIAN NODULE OF UPPER" />
      </concept>
      <concept>
        <code value="OMIM:151640" />
        <display value="LIP, HAMARTOMATOUS" />
      </concept>
      <concept>
        <code value="OMIM:151660" />
        <display value="LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:151700" />
        <display value="LIPOMA OF THE CONJUNCTIVA" />
      </concept>
      <concept>
        <code value="OMIM:151800" />
        <display value="LIPOMATOSIS, MULTIPLE SYMMETRIC" />
      </concept>
      <concept>
        <code value="OMIM:151900" />
        <display value="LIPOMATOSIS, MULTIPLE" />
      </concept>
      <concept>
        <code value="OMIM:152100" />
        <display value="LIPOPROTEIN TYPES--Ld SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:152200" />
        <display value="APOLIPOPROTEIN(a)" />
      </concept>
      <concept>
        <code value="OMIM:152300" />
        <display value="LIPOPROTEIN TYPES--Lt SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:152400" />
        <display value="LIPOPROTEIN, VARIANT OF BETA" />
      </concept>
      <concept>
        <code value="OMIM:152420" />
        <display value="LITHIUM TRANSPORT" />
      </concept>
      <concept>
        <code value="OMIM:152430" />
        <display value="LONGEVITY 1" />
      </concept>
      <concept>
        <code value="OMIM:152450" />
        <display value="LOW DENSITY LIPOPROTEIN, VARIATION IN MOLECULAR WEIGHT OF" />
      </concept>
      <concept>
        <code value="OMIM:152550" />
        <display value="LUMBAR STENOSIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:152600" />
        <display value="LUNULAE OF FINGERNAILS" />
      </concept>
      <concept>
        <code value="OMIM:152700" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS" />
      </concept>
      <concept>
        <code value="OMIM:152800" />
        <display value="LYMPHANGIECTASIA, INTESTINAL" />
      </concept>
      <concept>
        <code value="OMIM:152900" />
        <display value="LYMPHEDEMA AND CEREBRAL ARTERIOVENOUS ANOMALY" />
      </concept>
      <concept>
        <code value="OMIM:152950" />
        <display value="MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:153100" />
        <display value="LYMPHEDEMA, HEREDITARY, IA" />
      </concept>
      <concept>
        <code value="OMIM:153200" />
        <display value="LYMPHEDEMA, HEREDITARY, II" />
      </concept>
      <concept>
        <code value="OMIM:153245" />
        <display value="LYMPHOID ENHANCER-BINDING FACTOR 1" />
      </concept>
      <concept>
        <code value="OMIM:153280" />
        <display value="LYMPHOCYTE CYTOSOL POLYPEPTIDE, 40-KD" />
      </concept>
      <concept>
        <code value="OMIM:153290" />
        <display value="LYMPHOCYTE CYTOSOL POLYPEPTIDE, 49-KD" />
      </concept>
      <concept>
        <code value="OMIM:153300" />
        <display value="YELLOW NAIL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:153400" />
        <display value="LYMPHEDEMA-DISTICHIASIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:153470" />
        <display value="MACROCEPHALY, BENIGN FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:153550" />
        <display value="CHROMOSOME 5q DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:153600" />
        <display value="MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:153630" />
        <display value="MACROGLOSSIA" />
      </concept>
      <concept>
        <code value="OMIM:153670" />
        <display value="BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:153700" />
        <display value="MACULAR DYSTROPHY, VITELLIFORM, 2" />
      </concept>
      <concept>
        <code value="OMIM:153800" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 2" />
      </concept>
      <concept>
        <code value="OMIM:153840" />
        <display value="MACULAR DYSTROPHY, VITELLIFORM, 1" />
      </concept>
      <concept>
        <code value="OMIM:153870" />
        <display value="MACULAR DYSTROPHY, CONCENTRIC ANNULAR" />
      </concept>
      <concept>
        <code value="OMIM:153880" />
        <display value="MACULAR DYSTROPHY, DOMINANT CYSTOID" />
      </concept>
      <concept>
        <code value="OMIM:153890" />
        <display value="MACULAR DYSTROPHY, FENESTRATED SHEEN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:154020" />
        <display value="HYPOMAGNESEMIA 2, RENAL" />
      </concept>
      <concept>
        <code value="OMIM:154230" />
        <display value="46,XY SEX REVERSAL 4" />
      </concept>
      <concept>
        <code value="OMIM:154275" />
        <display value="MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:154276" />
        <display value="MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:154300" />
        <display value="MALOCCLUSION DUE TO PROTUBERANT UPPER FRONT TEETH" />
      </concept>
      <concept>
        <code value="OMIM:154370" />
        <display value="MAMMASTATIN" />
      </concept>
      <concept>
        <code value="OMIM:154400" />
        <display value="ACROFACIAL DYSOSTOSIS 1, NAGER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:154500" />
        <display value="TREACHER COLLINS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:154570" />
        <display value="MANNOSE 6-PHOSPHATE RECEPTOR RECOGNITION DEFECT, LEBANESE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:154600" />
        <display value="MARCUS GUNN PHENOMENON" />
      </concept>
      <concept>
        <code value="OMIM:154700" />
        <display value="MARFAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:154750" />
        <display value="MARFANOID HYPERMOBILITY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:154780" />
        <display value="MARSHALL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:154800" />
        <display value="MASTOCYTOSIS, CUTANEOUS" />
      </concept>
      <concept>
        <code value="OMIM:154850" />
        <display value="MASTICATORY MUSCLES, HYPERTROPHY OF" />
      </concept>
      <concept>
        <code value="OMIM:155000" />
        <display value="MAXILLOFACIAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:155050" />
        <display value="MAXILLONASAL DYSPLASIA, BINDER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:155100" />
        <display value="MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS" />
      </concept>
      <concept>
        <code value="OMIM:155140" />
        <display value="MECKEL DIVERTICULUM" />
      </concept>
      <concept>
        <code value="OMIM:155145" />
        <display value="CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA" />
      </concept>
      <concept>
        <code value="OMIM:155150" />
        <display value="MEDIAN-ULNAR NERVE COMMUNICATIONS" />
      </concept>
      <concept>
        <code value="OMIM:155200" />
        <display value="MEDIOSTERNAL DEPIGMENTATION LINE" />
      </concept>
      <concept>
        <code value="OMIM:155240" />
        <display value="THYROID CARCINOMA, FAMILIAL MEDULLARY" />
      </concept>
      <concept>
        <code value="OMIM:155255" />
        <display value="MEDULLOBLASTOMA" />
      </concept>
      <concept>
        <code value="OMIM:155310" />
        <display value="VISCERAL MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:155350" />
        <display value="MEGALENCEPHALY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:155500" />
        <display value="MACRODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:155600" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:155601" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:155700" />
        <display value="MELANOMA, MALIGNANT FAMILIAL INTRAOCULAR" />
      </concept>
      <concept>
        <code value="OMIM:155720" />
        <display value="MELANOMA, UVEAL" />
      </concept>
      <concept>
        <code value="OMIM:155755" />
        <display value="MELANOMA-ASTROCYTOMA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:155770" />
        <display value="MELANOMA TUMOR ANTIGEN GP90" />
      </concept>
      <concept>
        <code value="OMIM:155900" />
        <display value="MELKERSSON-ROSENTHAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:155950" />
        <display value="MELORHEOSTOSIS, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:155980" />
        <display value="MEMBRANOUS CRANIAL OSSIFICATION, DELAYED" />
      </concept>
      <concept>
        <code value="OMIM:156000" />
        <display value="MENIERE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:156190" />
        <display value="MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA" />
      </concept>
      <concept>
        <code value="OMIM:156200" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:156220" />
        <display value="MERALGIA PARAESTHETICA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:156230" />
        <display value="MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:156232" />
        <display value="MESOMELIC DYSPLASIA, KANTAPUTRA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:156240" />
        <display value="MESOTHELIOMA, MALIGNANT" />
      </concept>
      <concept>
        <code value="OMIM:156250" />
        <display value="METACHONDROMATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:156300" />
        <display value="METACHROMASIA OF FIBROBLASTS" />
      </concept>
      <concept>
        <code value="OMIM:156310" />
        <display value="METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASE A" />
      </concept>
      <concept>
        <code value="OMIM:156400" />
        <display value="METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:156500" />
        <display value="METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE" />
      </concept>
      <concept>
        <code value="OMIM:156510" />
        <display value="METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA WITH OR WITHOUT BRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:156520" />
        <display value="METATARSUS VARUS, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:156530" />
        <display value="METATROPIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:156550" />
        <display value="KNIEST DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:156580" />
        <display value="MICROCEPHALY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:156600" />
        <display value="MICROCORIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:156610" />
        <display value="SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:156620" />
        <display value="MICROCEPHALY-DEAFNESS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:156700" />
        <display value="MICROCORNEA, GLAUCOMA, AND ABSENT FRONTAL SINUSES" />
      </concept>
      <concept>
        <code value="OMIM:156810" />
        <display value="MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION" />
      </concept>
      <concept>
        <code value="OMIM:156830" />
        <display value="MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL" />
      </concept>
      <concept>
        <code value="OMIM:156850" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH CATARACT 1" />
      </concept>
      <concept>
        <code value="OMIM:156900" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH CORECTOPIA" />
      </concept>
      <concept>
        <code value="OMIM:157150" />
        <display value="MICROSPHEROPHAKIA WITH HERNIA" />
      </concept>
      <concept>
        <code value="OMIM:157151" />
        <display value="MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:157170" />
        <display value="HOLOPROSENCEPHALY 2" />
      </concept>
      <concept>
        <code value="OMIM:157200" />
        <display value="MIDPHALANGEAL HAIR" />
      </concept>
      <concept>
        <code value="OMIM:157300" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:157400" />
        <display value="MILIA, MULTIPLE ERUPTIVE" />
      </concept>
      <concept>
        <code value="OMIM:157600" />
        <display value="MIRROR MOVEMENTS 1" />
      </concept>
      <concept>
        <code value="OMIM:157640" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:157700" />
        <display value="MITRAL VALVE PROLAPSE 1" />
      </concept>
      <concept>
        <code value="OMIM:157800" />
        <display value="CARDIOSPONDYLOCARPOFACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:157900" />
        <display value="MOEBIUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:157950" />
        <display value="PERMANENT MOLARS, SECONDARY RETENTION OF" />
      </concept>
      <concept>
        <code value="OMIM:157960" />
        <display value="MOLONEY LEUKEMIA VIRUS INTEGRATION SITE 2, MOUSE, HOMOLOG OF" />
      </concept>
      <concept>
        <code value="OMIM:157980" />
        <display value="MOMO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:158000" />
        <display value="MONILETHRIX" />
      </concept>
      <concept>
        <code value="OMIM:158030" />
        <display value="ANTIGEN DEFINED BY MONOCLONAL ANTIBODY AJ9" />
      </concept>
      <concept>
        <code value="OMIM:158040" />
        <display value="ANTIGEN DEFINED BY MONOCLONAL ANTIBODY T87" />
      </concept>
      <concept>
        <code value="OMIM:158050" />
        <display value="MONKEY RED BLOOD CELL RECEPTOR" />
      </concept>
      <concept>
        <code value="OMIM:158100" />
        <display value="MONOPHALANGY OF GREAT TOE" />
      </concept>
      <concept>
        <code value="OMIM:158105" />
        <display value="CHEMOKINE, CC MOTIF, LIGAND 2" />
      </concept>
      <concept>
        <code value="OMIM:158170" />
        <display value="CHROMOSOME 9p DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:158250" />
        <display value="NONDISJUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:158280" />
        <display value="MOTION SICKNESS" />
      </concept>
      <concept>
        <code value="OMIM:158300" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:158310" />
        <display value="MUCOEPITHELIAL DYSPLASIA, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:158320" />
        <display value="MUIR-TORRE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:158330" />
        <display value="MULLERIAN APLASIA AND HYPERANDROGENISM" />
      </concept>
      <concept>
        <code value="OMIM:158345" />
        <display value="MULTIPLE EXOSTOSES WITH SPASTIC TETRAPARESIS" />
      </concept>
      <concept>
        <code value="OMIM:158350" />
        <display value="COWDEN SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:158400" />
        <display value="MUSCLE CRAMPS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:158500" />
        <display value="MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS" />
      </concept>
      <concept>
        <code value="OMIM:158580" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA" />
      </concept>
      <concept>
        <code value="OMIM:158590" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA" />
      </concept>
      <concept>
        <code value="OMIM:158600" />
        <display value="SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:158650" />
        <display value="MUSCULAR ATROPHY, MALIGNANT NEUROGENIC" />
      </concept>
      <concept>
        <code value="OMIM:158800" />
        <display value="MUSCULAR DYSTROPHY, BARNES TYPE" />
      </concept>
      <concept>
        <code value="OMIM:158810" />
        <display value="BETHLEM MYOPATHY 1" />
      </concept>
      <concept>
        <code value="OMIM:158900" />
        <display value="FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1" />
      </concept>
      <concept>
        <code value="OMIM:158901" />
        <display value="FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2" />
      </concept>
      <concept>
        <code value="OMIM:159050" />
        <display value="MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, WITH INTERNALIZED CAPILLARIES" />
      </concept>
      <concept>
        <code value="OMIM:159100" />
        <display value="MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE" />
      </concept>
      <concept>
        <code value="OMIM:159300" />
        <display value="MUSICAL PERFECT PITCH" />
      </concept>
      <concept>
        <code value="OMIM:159400" />
        <display value="MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE" />
      </concept>
      <concept>
        <code value="OMIM:159410" />
        <display value="MYDRIATIC RESPONSE TO PHARMACOLOGIC AGENTS" />
      </concept>
      <concept>
        <code value="OMIM:159420" />
        <display value="MYDRIASIS, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:159500" />
        <display value="MYELINATED OPTIC NERVE FIBERS" />
      </concept>
      <concept>
        <code value="OMIM:159550" />
        <display value="ATAXIA-PANCYTOPENIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:159555" />
        <display value="LYSINE-SPECIFIC METHYLTRANSFERASE 2A" />
      </concept>
      <concept>
        <code value="OMIM:159580" />
        <display value="MYELOPATHY, HTLV-1-ASSOCIATED" />
      </concept>
      <concept>
        <code value="OMIM:159595" />
        <display value="MYELOPROLIFERATIVE SYNDROME, TRANSIENT" />
      </concept>
      <concept>
        <code value="OMIM:159600" />
        <display value="MYOCLONIC EPILEPSY, HARTUNG TYPE" />
      </concept>
      <concept>
        <code value="OMIM:159700" />
        <display value="MYOCLONUS AND ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:159800" />
        <display value="MYOCLONUS, CEREBELLAR ATAXIA, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:159900" />
        <display value="DYSTONIA 11, MYOCLONIC" />
      </concept>
      <concept>
        <code value="OMIM:159950" />
        <display value="SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY" />
      </concept>
      <concept>
        <code value="OMIM:160010" />
        <display value="MYOGLOBINURIA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:160120" />
        <display value="EPISODIC ATAXIA, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:160150" />
        <display value="MYOPATHY, CENTRONUCLEAR, 1" />
      </concept>
      <concept>
        <code value="OMIM:160300" />
        <display value="MYOPATHY, DISTAL, INFANTILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:160500" />
        <display value="MYOPATHY, DISTAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:160565" />
        <display value="MYOPATHY, TUBULAR AGGREGATE, 1" />
      </concept>
      <concept>
        <code value="OMIM:160570" />
        <display value="MYOPATHY WITH STORAGE OF GLYCOPROTEINS AND GLYCOSAMINOGLYCANS" />
      </concept>
      <concept>
        <code value="OMIM:160700" />
        <display value="MYOPIA 2, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:160750" />
        <display value="MYOSITIS" />
      </concept>
      <concept>
        <code value="OMIM:160800" />
        <display value="MYOTONIA CONGENITA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:160900" />
        <display value="MYOTONIC DYSTROPHY 1" />
      </concept>
      <concept>
        <code value="OMIM:160980" />
        <display value="CARNEY COMPLEX, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:160990" />
        <display value="MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS" />
      </concept>
      <concept>
        <code value="OMIM:161000" />
        <display value="NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:161050" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:161070" />
        <display value="NAIL HIGH-SULFUR PROTEIN" />
      </concept>
      <concept>
        <code value="OMIM:161080" />
        <display value="NAIL LOW-SULFUR PROTEIN" />
      </concept>
      <concept>
        <code value="OMIM:161100" />
        <display value="NAILBEDS, PIGMENTATION OF" />
      </concept>
      <concept>
        <code value="OMIM:161200" />
        <display value="NAIL-PATELLA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:161400" />
        <display value="NARCOLEPSY 1" />
      </concept>
      <concept>
        <code value="OMIM:161470" />
        <display value="NASAL ALAR COLLAPSE, BILATERAL" />
      </concept>
      <concept>
        <code value="OMIM:161480" />
        <display value="NASAL BONES, ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:161500" />
        <display value="NASAL GROOVE, FAMILIAL TRANSVERSE" />
      </concept>
      <concept>
        <code value="OMIM:161530" />
        <display value="NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE" />
      </concept>
      <concept>
        <code value="OMIM:161550" />
        <display value="NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:161600" />
        <display value="NAVICULAR BONE, ACCESSORY" />
      </concept>
      <concept>
        <code value="OMIM:161700" />
        <display value="NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT" />
      </concept>
      <concept>
        <code value="OMIM:161800" />
        <display value="NEMALINE MYOPATHY 3" />
      </concept>
      <concept>
        <code value="OMIM:161900" />
        <display value="RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION" />
      </concept>
      <concept>
        <code value="OMIM:161950" />
        <display value="IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:162000" />
        <display value="HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1" />
      </concept>
      <concept>
        <code value="OMIM:162020" />
        <display value="NERVE GROWTH FACTOR, ALPHA SUBUNIT" />
      </concept>
      <concept>
        <code value="OMIM:162091" />
        <display value="SCHWANNOMATOSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:162100" />
        <display value="AMYOTROPHY, HEREDITARY NEURALGIC" />
      </concept>
      <concept>
        <code value="OMIM:162200" />
        <display value="NEUROFIBROMATOSIS, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:162210" />
        <display value="NEUROFIBROMATOSIS, FAMILIAL SPINAL" />
      </concept>
      <concept>
        <code value="OMIM:162240" />
        <display value="NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:162260" />
        <display value="NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL" />
      </concept>
      <concept>
        <code value="OMIM:162270" />
        <display value="NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI" />
      </concept>
      <concept>
        <code value="OMIM:162300" />
        <display value="MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB" />
      </concept>
      <concept>
        <code value="OMIM:162350" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:162370" />
        <display value="NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX" />
      </concept>
      <concept>
        <code value="OMIM:162380" />
        <display value="NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE" />
      </concept>
      <concept>
        <code value="OMIM:162400" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:162500" />
        <display value="NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES" />
      </concept>
      <concept>
        <code value="OMIM:162600" />
        <display value="NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE" />
      </concept>
      <concept>
        <code value="OMIM:162700" />
        <display value="NEUTROPENIA, CHRONIC FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:162800" />
        <display value="CYCLIC NEUTROPENIA" />
      </concept>
      <concept>
        <code value="OMIM:162820" />
        <display value="NEUTROPHIL MIGRATION" />
      </concept>
      <concept>
        <code value="OMIM:162830" />
        <display value="NEUTROPHILIA, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:162880" />
        <display value="NEUTROPHIL-SPECIFIC ANTIGEN: ND1" />
      </concept>
      <concept>
        <code value="OMIM:162900" />
        <display value="NEVUS, EPIDERMAL" />
      </concept>
      <concept>
        <code value="OMIM:163000" />
        <display value="CAPILLARY MALFORMATIONS, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:163050" />
        <display value="NEVUS ANEMICUS" />
      </concept>
      <concept>
        <code value="OMIM:163100" />
        <display value="NEVUS FLAMMEUS OF NAPE OF NECK" />
      </concept>
      <concept>
        <code value="OMIM:163200" />
        <display value="SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:163400" />
        <display value="NIEVERGELT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:163500" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:163600" />
        <display value="NIPPLES INVERTED" />
      </concept>
      <concept>
        <code value="OMIM:163700" />
        <display value="NIPPLES, SUPERNUMERARY" />
      </concept>
      <concept>
        <code value="OMIM:163729" />
        <display value="NITRIC OXIDE SYNTHASE 3" />
      </concept>
      <concept>
        <code value="OMIM:163800" />
        <display value="SICK SINUS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:163850" />
        <display value="NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:163950" />
        <display value="NOONAN SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:164000" />
        <display value="NOSE, ANOMALOUS SHAPE OF" />
      </concept>
      <concept>
        <code value="OMIM:164100" />
        <display value="NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:164150" />
        <display value="NYSTAGMUS, HEREDITARY VERTICAL" />
      </concept>
      <concept>
        <code value="OMIM:164170" />
        <display value="NYSTAGMUS, VOLUNTARY" />
      </concept>
      <concept>
        <code value="OMIM:164180" />
        <display value="OCULOCEREBROCUTANEOUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:164185" />
        <display value="OCULAR CICATRICIAL PEMPHIGOID" />
      </concept>
      <concept>
        <code value="OMIM:164190" />
        <display value="OCULAR DOMINANCE" />
      </concept>
      <concept>
        <code value="OMIM:164200" />
        <display value="OCULODENTODIGITAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:164210" />
        <display value="HEMIFACIAL MICROSOMIA" />
      </concept>
      <concept>
        <code value="OMIM:164220" />
        <display value="SCHILBACH-ROTT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:164230" />
        <display value="OBSESSIVE-COMPULSIVE DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:164280" />
        <display value="FEINGOLD SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:164300" />
        <display value="OCULOPHARYNGEAL MUSCULAR DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:164310" />
        <display value="OCULOPHARYNGODISTAL MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:164330" />
        <display value="ODONTOMA-DYSPHAGIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:164400" />
        <display value="SPINOCEREBELLAR ATAXIA 1" />
      </concept>
      <concept>
        <code value="OMIM:164500" />
        <display value="SPINOCEREBELLAR ATAXIA 7" />
      </concept>
      <concept>
        <code value="OMIM:164680" />
        <display value="ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR" />
      </concept>
      <concept>
        <code value="OMIM:164700" />
        <display value="OLIVOPONTOCEREBELLAR ATROPHY V" />
      </concept>
      <concept>
        <code value="OMIM:164745" />
        <display value="OMODYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:164750" />
        <display value="OMPHALOCELE, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:164800" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:164900" />
        <display value="OPHTHALMOMANDIBULOMELIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:165000" />
        <display value="OPHTHALMOPLEGIA, FAMILIAL STATIC" />
      </concept>
      <concept>
        <code value="OMIM:165098" />
        <display value="OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION" />
      </concept>
      <concept>
        <code value="OMIM:165150" />
        <display value="OPHTHALMOPLEGIA, PROGRESSIVE, WITH SCROTAL TONGUE AND MENTAL DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:165199" />
        <display value="OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:165200" />
        <display value="OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS" />
      </concept>
      <concept>
        <code value="OMIM:165210" />
        <display value="ONCOGENE BMYC" />
      </concept>
      <concept>
        <code value="OMIM:165290" />
        <display value="ONCOGENE RMYC" />
      </concept>
      <concept>
        <code value="OMIM:165300" />
        <display value="OPTIC ATROPHY 3, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:165500" />
        <display value="OPTIC ATROPHY 1" />
      </concept>
      <concept>
        <code value="OMIM:165510" />
        <display value="OPTIC ATROPHY WITH NEGATIVE ELECTRORETINOGRAMS" />
      </concept>
      <concept>
        <code value="OMIM:165550" />
        <display value="OPTIC NERVE HYPOPLASIA, BILATERAL" />
      </concept>
      <concept>
        <code value="OMIM:165590" />
        <display value="OROFACIODIGITAL SYNDROME X" />
      </concept>
      <concept>
        <code value="OMIM:165600" />
        <display value="ORBITAL MARGIN, HYPOPLASIA OF" />
      </concept>
      <concept>
        <code value="OMIM:165660" />
        <display value="OSLAM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:165670" />
        <display value="OSSIFIED EAR CARTILAGES" />
      </concept>
      <concept>
        <code value="OMIM:165680" />
        <display value="OSSICULAR MALFORMATIONS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:165700" />
        <display value="THIEMANN DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:165720" />
        <display value="OSTEOARTHRITIS SUSCEPTIBILITY 1" />
      </concept>
      <concept>
        <code value="OMIM:165800" />
        <display value="SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS" />
      </concept>
      <concept>
        <code value="OMIM:166000" />
        <display value="ENCHONDROMATOSIS, MULTIPLE, OLLIER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:166200" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:166210" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:166220" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:166230" />
        <display value="OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES" />
      </concept>
      <concept>
        <code value="OMIM:166250" />
        <display value="OSTEOGLOPHONIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:166260" />
        <display value="GNATHODIAPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:166300" />
        <display value="MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:166350" />
        <display value="OSSEOUS HETEROPLASIA, PROGRESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:166400" />
        <display value="OSTEOMAS OF MANDIBLE" />
      </concept>
      <concept>
        <code value="OMIM:166450" />
        <display value="OSTEOMESOPYKNOSIS" />
      </concept>
      <concept>
        <code value="OMIM:166600" />
        <display value="OSTEOPETROSIS, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:166700" />
        <display value="BUSCHKE-OLLENDORFF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:166705" />
        <display value="OSTEOPOIKILOSIS AND DACRYOCYSTITIS" />
      </concept>
      <concept>
        <code value="OMIM:166710" />
        <display value="OSTEOPOROSIS" />
      </concept>
      <concept>
        <code value="OMIM:166740" />
        <display value="OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES" />
      </concept>
      <concept>
        <code value="OMIM:166750" />
        <display value="OTODENTAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:166760" />
        <display value="OTITIS MEDIA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:166780" />
        <display value="OTOFACIOCERVICAL SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:166800" />
        <display value="OTOSCLEROSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:166900" />
        <display value="OVALOCYTOSIS, SOUTHEAST ASIAN" />
      </concept>
      <concept>
        <code value="OMIM:166910" />
        <display value="OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS" />
      </concept>
      <concept>
        <code value="OMIM:166950" />
        <display value="TERATOMA, OVARIAN" />
      </concept>
      <concept>
        <code value="OMIM:166970" />
        <display value="OVARIAN FIBROMATA" />
      </concept>
      <concept>
        <code value="OMIM:166990" />
        <display value="OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA, HYDROCEPHALUS, AND HYPERTENSION" />
      </concept>
      <concept>
        <code value="OMIM:167000" />
        <display value="OVARIAN CANCER" />
      </concept>
      <concept>
        <code value="OMIM:167030" />
        <display value="NEPHROLITHIASIS, CALCIUM OXALATE" />
      </concept>
      <concept>
        <code value="OMIM:167100" />
        <display value="HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:167200" />
        <display value="PACHYONYCHIA CONGENITA 1" />
      </concept>
      <concept>
        <code value="OMIM:167210" />
        <display value="PACHYONYCHIA CONGENITA 2" />
      </concept>
      <concept>
        <code value="OMIM:167220" />
        <display value="PACMAN DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:167250" />
        <display value="PAGET DISEASE OF BONE 3" />
      </concept>
      <concept>
        <code value="OMIM:167300" />
        <display value="PAGET DISEASE, EXTRAMAMMARY" />
      </concept>
      <concept>
        <code value="OMIM:167320" />
        <display value="INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1" />
      </concept>
      <concept>
        <code value="OMIM:167400" />
        <display value="PAROXYSMAL EXTREME PAIN DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:167500" />
        <display value="PALATOPHARYNGEAL INCOMPETENCE" />
      </concept>
      <concept>
        <code value="OMIM:167600" />
        <display value="PALMARIS LONGUS MUSCLE, ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:167700" />
        <display value="PALMOMENTAL REFLEX" />
      </concept>
      <concept>
        <code value="OMIM:167730" />
        <display value="NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:167750" />
        <display value="PANCREAS, ANNULAR" />
      </concept>
      <concept>
        <code value="OMIM:167755" />
        <display value="PANCREAS, DORSAL, AGENESIS OF" />
      </concept>
      <concept>
        <code value="OMIM:167800" />
        <display value="PANCREATITIS, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:167850" />
        <display value="PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:167870" />
        <display value="PANIC DISORDER 1" />
      </concept>
      <concept>
        <code value="OMIM:167900" />
        <display value="PAPILLOMATOSIS, CONFLUENT AND RETICULATED" />
      </concept>
      <concept>
        <code value="OMIM:167950" />
        <display value="PAPILLOMATOSIS, FLORID, OF NIPPLE" />
      </concept>
      <concept>
        <code value="OMIM:167959" />
        <display value="HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 1" />
      </concept>
      <concept>
        <code value="OMIM:167960" />
        <display value="HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 2" />
      </concept>
      <concept>
        <code value="OMIM:168000" />
        <display value="PARAGANGLIOMAS 1" />
      </concept>
      <concept>
        <code value="OMIM:168100" />
        <display value="PARALYSIS AGITANS, JUVENILE, OF HUNT" />
      </concept>
      <concept>
        <code value="OMIM:168200" />
        <display value="PARAMOLAR TUBERCLE OF BOLK" />
      </concept>
      <concept>
        <code value="OMIM:168300" />
        <display value="PARAMYOTONIA CONGENITA OF VON EULENBURG" />
      </concept>
      <concept>
        <code value="OMIM:168400" />
        <display value="PARASTREMMATIC DWARFISM" />
      </concept>
      <concept>
        <code value="OMIM:168500" />
        <display value="PARIETAL FORAMINA 1" />
      </concept>
      <concept>
        <code value="OMIM:168550" />
        <display value="PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:168600" />
        <display value="PARKINSON DISEASE, LATE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:168601" />
        <display value="PARKINSON DISEASE 1, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:168605" />
        <display value="PERRY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:168710" />
        <display value="PAROTID PROLINE-RICH SALIVARY PROTEIN Pc" />
      </concept>
      <concept>
        <code value="OMIM:168800" />
        <display value="PAROTIDOMEGALY, HEREDITARY BILATERAL" />
      </concept>
      <concept>
        <code value="OMIM:168820" />
        <display value="PARAOXONASE 1" />
      </concept>
      <concept>
        <code value="OMIM:168830" />
        <display value="PASSOVOY FACTOR DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:168860" />
        <display value="PATELLA APLASIA-HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:168885" />
        <display value="PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:168900" />
        <display value="PATELLA, CHONDROMALACIA OF" />
      </concept>
      <concept>
        <code value="OMIM:169000" />
        <display value="PATELLA, FAMILIAL RECURRENT DISLOCATION OF" />
      </concept>
      <concept>
        <code value="OMIM:169100" />
        <display value="CHAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:169150" />
        <display value="MACULAR DYSTROPHY, PATTERNED, 1" />
      </concept>
      <concept>
        <code value="OMIM:169170" />
        <display value="PATTERSON PSEUDOLEPRECHAUNISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:169200" />
        <display value="PECHET FACTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:169300" />
        <display value="PECTUS EXCAVATUM" />
      </concept>
      <concept>
        <code value="OMIM:169400" />
        <display value="PELGER-HUET ANOMALY" />
      </concept>
      <concept>
        <code value="OMIM:169500" />
        <display value="LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:169545" />
        <display value="PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA" />
      </concept>
      <concept>
        <code value="OMIM:169550" />
        <display value="PELVIS-SHOULDER DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:169600" />
        <display value="BENIGN CHRONIC PEMPHIGUS" />
      </concept>
      <concept>
        <code value="OMIM:169610" />
        <display value="PEMPHIGUS VULGARIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:169710" />
        <display value="PEPSINOGEN 3, GROUP I" />
      </concept>
      <concept>
        <code value="OMIM:170100" />
        <display value="PROLIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:170390" />
        <display value="ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS" />
      </concept>
      <concept>
        <code value="OMIM:170400" />
        <display value="HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:170500" />
        <display value="HYPERKALEMIC PERIODIC PARALYSIS" />
      </concept>
      <concept>
        <code value="OMIM:170600" />
        <display value="NORMOKALEMIC PERIODIC PARALYSIS" />
      </concept>
      <concept>
        <code value="OMIM:170650" />
        <display value="PERIODONTITIS, AGGRESSIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:170700" />
        <display value="PERIPHERAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:170900" />
        <display value="PERNICIOUS ANEMIA" />
      </concept>
      <concept>
        <code value="OMIM:170980" />
        <display value="PERONEAL NERVE, ACCESSORY DEEP" />
      </concept>
      <concept>
        <code value="OMIM:170990" />
        <display value="PEROXIDASE, SALIVARY" />
      </concept>
      <concept>
        <code value="OMIM:170998" />
        <display value="PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-ALPHA" />
      </concept>
      <concept>
        <code value="OMIM:171000" />
        <display value="PEYRONIE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:171100" />
        <display value="PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN" />
      </concept>
      <concept>
        <code value="OMIM:171200" />
        <display value="THIOUREA TASTING" />
      </concept>
      <concept>
        <code value="OMIM:171300" />
        <display value="PHEOCHROMOCYTOMA" />
      </concept>
      <concept>
        <code value="OMIM:171400" />
        <display value="MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA" />
      </concept>
      <concept>
        <code value="OMIM:171420" />
        <display value="PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:171450" />
        <display value="PHLEBECTASIA OF LIPS" />
      </concept>
      <concept>
        <code value="OMIM:171480" />
        <display value="PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA" />
      </concept>
      <concept>
        <code value="OMIM:171660" />
        <display value="PHOSPHATASE, ACID, OF TISSUES" />
      </concept>
      <concept>
        <code value="OMIM:171720" />
        <display value="ALKALINE PHOSPHATASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:172110" />
        <display value="PHOSPHOGLUCOMUTASE 4" />
      </concept>
      <concept>
        <code value="OMIM:172150" />
        <display value="6-PHOSPHOGLUCONOLACTONASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:172290" />
        <display value="PHOSPHOGLYCOPROTEIN 1" />
      </concept>
      <concept>
        <code value="OMIM:172425" />
        <display value="PHOSPHOLIPID TRANSFER PROTEIN" />
      </concept>
      <concept>
        <code value="OMIM:172500" />
        <display value="PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:172700" />
        <display value="PICK DISEASE OF BRAIN" />
      </concept>
      <concept>
        <code value="OMIM:172800" />
        <display value="PIEBALD TRAIT" />
      </concept>
      <concept>
        <code value="OMIM:172850" />
        <display value="PIEBALD TRAIT WITH NEUROLOGIC DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:172870" />
        <display value="PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:172880" />
        <display value="PIERRE ROBIN SYNDROME AND OLIGODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:172900" />
        <display value="PIGMENTED PURPURIC ERUPTION" />
      </concept>
      <concept>
        <code value="OMIM:173000" />
        <display value="PILONIDAL SINUS" />
      </concept>
      <concept>
        <code value="OMIM:173100" />
        <display value="ISOLATED GROWTH HORMONE DEFICIENCY, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:173200" />
        <display value="PITYRIASIS RUBRA PILARIS" />
      </concept>
      <concept>
        <code value="OMIM:173395" />
        <display value="PLATELET ADENYLATE CYCLASE ACTIVITY" />
      </concept>
      <concept>
        <code value="OMIM:173400" />
        <display value="PLATELET AGGREGATION, SPONTANEOUS" />
      </concept>
      <concept>
        <code value="OMIM:173420" />
        <display value="PLATELET DISORDER, UNDEFINED" />
      </concept>
      <concept>
        <code value="OMIM:173450" />
        <display value="PLATELET FACTOR 3 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:173500" />
        <display value="PLATELET GROUPS--Ko SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:173540" />
        <display value="PLATELET GROUPS--Pl(E) SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:173560" />
        <display value="PLATELET MEMBRANE FLUIDITY" />
      </concept>
      <concept>
        <code value="OMIM:173580" />
        <display value="PLATELET RESPONSIVENESS TO ADRENALINE, DEPRESSED" />
      </concept>
      <concept>
        <code value="OMIM:173590" />
        <display value="PLATELET SIGNAL PROCESSING DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:173600" />
        <display value="PNEUMOTHORAX, PRIMARY SPONTANEOUS" />
      </concept>
      <concept>
        <code value="OMIM:173650" />
        <display value="KINDLER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:173700" />
        <display value="POIKILODERMA, HEREDITARY SCLEROSING" />
      </concept>
      <concept>
        <code value="OMIM:173800" />
        <display value="POLAND SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:173900" />
        <display value="POLYCYSTIC KIDNEY DISEASE 1 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:174000" />
        <display value="MEDULLARY CYSTIC KIDNEY DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:174050" />
        <display value="POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:174200" />
        <display value="POLYDACTYLY, POSTAXIAL, TYPE A1" />
      </concept>
      <concept>
        <code value="OMIM:174300" />
        <display value="OROFACIODIGITAL SYNDROME V" />
      </concept>
      <concept>
        <code value="OMIM:174310" />
        <display value="POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA" />
      </concept>
      <concept>
        <code value="OMIM:174400" />
        <display value="POLYDACTYLY, PREAXIAL I" />
      </concept>
      <concept>
        <code value="OMIM:174500" />
        <display value="POLYDACTYLY, PREAXIAL II" />
      </concept>
      <concept>
        <code value="OMIM:174600" />
        <display value="POLYDACTYLY, PREAXIAL III" />
      </concept>
      <concept>
        <code value="OMIM:174700" />
        <display value="POLYDACTYLY, PREAXIAL IV" />
      </concept>
      <concept>
        <code value="OMIM:174750" />
        <display value="POLYKARYOCYTOSIS INDUCER" />
      </concept>
      <concept>
        <code value="OMIM:174770" />
        <display value="ACTINIC PRURIGO" />
      </concept>
      <concept>
        <code value="OMIM:174800" />
        <display value="MCCUNE-ALBRIGHT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:174810" />
        <display value="FAMILIAL EXPANSILE OSTEOLYSIS" />
      </concept>
      <concept>
        <code value="OMIM:174900" />
        <display value="JUVENILE POLYPOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:175020" />
        <display value="POLYPOSIS, GASTRIC" />
      </concept>
      <concept>
        <code value="OMIM:175050" />
        <display value="JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:175100" />
        <display value="FAMILIAL ADENOMATOUS POLYPOSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:175200" />
        <display value="PEUTZ-JEGHERS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:175400" />
        <display value="POLYPOSIS, INTESTINAL, SCATTERED AND DISCRETE" />
      </concept>
      <concept>
        <code value="OMIM:175450" />
        <display value="POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES" />
      </concept>
      <concept>
        <code value="OMIM:175500" />
        <display value="POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES" />
      </concept>
      <concept>
        <code value="OMIM:175505" />
        <display value="POLYPOSIS OF GASTRIC FUNDUS WITHOUT POLYPOSIS COLI" />
      </concept>
      <concept>
        <code value="OMIM:175510" />
        <display value="POLYPS, MULTIPLE AND RECURRENT INFLAMMATORY FIBROID, GASTROINTESTINAL" />
      </concept>
      <concept>
        <code value="OMIM:175690" />
        <display value="POLYSYNDACTYLY, CROSSED" />
      </concept>
      <concept>
        <code value="OMIM:175700" />
        <display value="GREIG CEPHALOPOLYSYNDACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:175750" />
        <display value="POPLITEAL CYST" />
      </concept>
      <concept>
        <code value="OMIM:175780" />
        <display value="PORENCEPHALY 1" />
      </concept>
      <concept>
        <code value="OMIM:175800" />
        <display value="POROKERATOSIS 1, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:175850" />
        <display value="POROKERATOSIS 2, PALMAR, PLANTAR, AND DISSEMINATED TYPE" />
      </concept>
      <concept>
        <code value="OMIM:175860" />
        <display value="PALMOPLANTAR KERATODERMA, PUNCTATE TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:175900" />
        <display value="POROKERATOSIS 3, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:176000" />
        <display value="PORPHYRIA, ACUTE INTERMITTENT" />
      </concept>
      <concept>
        <code value="OMIM:176090" />
        <display value="PORPHYRIA CUTANEA TARDA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:176100" />
        <display value="PORPHYRIA CUTANEA TARDA" />
      </concept>
      <concept>
        <code value="OMIM:176200" />
        <display value="PORPHYRIA VARIEGATA" />
      </concept>
      <concept>
        <code value="OMIM:176240" />
        <display value="POSTAXIAL OLIGODACTYLY, TETRAMELIC" />
      </concept>
      <concept>
        <code value="OMIM:176250" />
        <display value="POSTERIOR COLUMN ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:176270" />
        <display value="PRADER-WILLI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:176305" />
        <display value="PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS" />
      </concept>
      <concept>
        <code value="OMIM:176400" />
        <display value="PRECOCIOUS PUBERTY, CENTRAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:176410" />
        <display value="PRECOCIOUS PUBERTY, MALE-LIMITED" />
      </concept>
      <concept>
        <code value="OMIM:176430" />
        <display value="PREMATURE CHROMATID SEPARATION TRAIT" />
      </concept>
      <concept>
        <code value="OMIM:176450" />
        <display value="CURRARINO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:176500" />
        <display value="CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1" />
      </concept>
      <concept>
        <code value="OMIM:176600" />
        <display value="PRESENILE DEMENTIA, KRAEPELIN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:176620" />
        <display value="PRIAPISM, FAMILIAL IDIOPATHIC" />
      </concept>
      <concept>
        <code value="OMIM:176630" />
        <display value="PRIMARY RELEASE DISORDER OF PLATELETS" />
      </concept>
      <concept>
        <code value="OMIM:176670" />
        <display value="HUTCHINSON-GILFORD PROGERIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:176690" />
        <display value="PROGEROID SHORT STATURE WITH PIGMENTED NEVI" />
      </concept>
      <concept>
        <code value="OMIM:176700" />
        <display value="PROGNATHISM, MANDIBULAR" />
      </concept>
      <concept>
        <code value="OMIM:176770" />
        <display value="PROLINE-NEGATIVE AUXOTROPH OF HAMSTER, COMPLEMENTATION OF" />
      </concept>
      <concept>
        <code value="OMIM:176780" />
        <display value="PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:176800" />
        <display value="PRONATION-SUPINATION OF THE FOREARM, IMPAIRMENT OF" />
      </concept>
      <concept>
        <code value="OMIM:176807" />
        <display value="PROSTATE CANCER" />
      </concept>
      <concept>
        <code value="OMIM:176860" />
        <display value="THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:176900" />
        <display value="PROTEOLYTIC CAPACITY OF PLASMA" />
      </concept>
      <concept>
        <code value="OMIM:176920" />
        <display value="PROTEUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:177000" />
        <display value="PROTOPORPHYRIA, ERYTHROPOIETIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:177050" />
        <display value="PROTRUSIO ACETABULI" />
      </concept>
      <concept>
        <code value="OMIM:177100" />
        <display value="PRURITUS, HEREDITARY LOCALIZED" />
      </concept>
      <concept>
        <code value="OMIM:177170" />
        <display value="PSEUDOACHONDROPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:177200" />
        <display value="LIDDLE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:177300" />
        <display value="PSEUDOARTHROGRYPOSIS" />
      </concept>
      <concept>
        <code value="OMIM:177350" />
        <display value="PSEUDOATROPHODERMA COLLI" />
      </concept>
      <concept>
        <code value="OMIM:177600" />
        <display value="PSEUDOCHOLINESTERASE, INCREASE IN PLASMA LEVEL OF" />
      </concept>
      <concept>
        <code value="OMIM:177650" />
        <display value="EXFOLIATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:177700" />
        <display value="GLAUCOMA 1, OPEN ANGLE, P" />
      </concept>
      <concept>
        <code value="OMIM:177735" />
        <display value="PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:177750" />
        <display value="PSEUDOMONILETHRIX" />
      </concept>
      <concept>
        <code value="OMIM:177800" />
        <display value="PSEUDOPAPILLEDEMA" />
      </concept>
      <concept>
        <code value="OMIM:177820" />
        <display value="PSEUDO-VON WILLEBRAND DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:177850" />
        <display value="PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE" />
      </concept>
      <concept>
        <code value="OMIM:177900" />
        <display value="PSORIASIS 1, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:177980" />
        <display value="PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:177990" />
        <display value="PTERYGIUM COLLI, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:178000" />
        <display value="PTERYGIUM OF CONJUNCTIVA AND CORNEA" />
      </concept>
      <concept>
        <code value="OMIM:178110" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 8" />
      </concept>
      <concept>
        <code value="OMIM:178200" />
        <display value="PTERYGIUM, ANTECUBITAL" />
      </concept>
      <concept>
        <code value="OMIM:178300" />
        <display value="PTOSIS, HEREDITARY CONGENITAL 1" />
      </concept>
      <concept>
        <code value="OMIM:178330" />
        <display value="PTOSIS, STRABISMUS, AND ECTOPIC PUPILS" />
      </concept>
      <concept>
        <code value="OMIM:178350" />
        <display value="PUBIC BONE DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:178370" />
        <display value="PULMONARY ATRESIA WITH VENTRICULAR SEPTAL DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:178400" />
        <display value="PULMONARY EDEMA OF MOUNTAINEERS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:178500" />
        <display value="PULMONARY FIBROSIS, IDIOPATHIC" />
      </concept>
      <concept>
        <code value="OMIM:178550" />
        <display value="PULMONARY HEMOSIDEROSIS" />
      </concept>
      <concept>
        <code value="OMIM:178600" />
        <display value="PULMONARY HYPERTENSION, PRIMARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:178610" />
        <display value="PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:178650" />
        <display value="PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHIC ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:178651" />
        <display value="PULMONIC STENOSIS AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:178800" />
        <display value="PUPIL, EGG-SHAPED" />
      </concept>
      <concept>
        <code value="OMIM:178900" />
        <display value="PUPILLARY MEMBRANE, PERSISTENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:178995" />
        <display value="PRURITIC URTICARIAL PAPULES AND PLAQUES OF PREGNANCY" />
      </concept>
      <concept>
        <code value="OMIM:179000" />
        <display value="PURPURA SIMPLEX" />
      </concept>
      <concept>
        <code value="OMIM:179010" />
        <display value="PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:179200" />
        <display value="RADIAL HEADS, POSTERIOR DISLOCATION OF" />
      </concept>
      <concept>
        <code value="OMIM:179250" />
        <display value="RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARY DIASTEMA" />
      </concept>
      <concept>
        <code value="OMIM:179270" />
        <display value="RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:179280" />
        <display value="RADIAL-RENAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:179300" />
        <display value="RADIOULNAR SYNOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:179400" />
        <display value="RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE" />
      </concept>
      <concept>
        <code value="OMIM:179450" />
        <display value="RAGWEED SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:179500" />
        <display value="RAINDROP HYPOPIGMENTATION" />
      </concept>
      <concept>
        <code value="OMIM:179600" />
        <display value="RAYNAUD DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:179613" />
        <display value="RECOMBINANT CHROMOSOME 8 SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:179620" />
        <display value="RAPH BLOOD GROUP SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:179650" />
        <display value="RED CELL PERMEABILITY DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:179700" />
        <display value="RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS" />
      </concept>
      <concept>
        <code value="OMIM:179800" />
        <display value="RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:179830" />
        <display value="RENAL TUBULAR ACIDOSIS, PROXIMAL" />
      </concept>
      <concept>
        <code value="OMIM:179840" />
        <display value="RETICULAR DYSTROPHY OF RETINAL PIGMENT EPITHELIUM" />
      </concept>
      <concept>
        <code value="OMIM:179850" />
        <display value="DOWLING-DEGOS DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:179900" />
        <display value="RETINAL APLASIA" />
      </concept>
      <concept>
        <code value="OMIM:180000" />
        <display value="RETINAL ARTERIES, TORTUOSITY OF" />
      </concept>
      <concept>
        <code value="OMIM:180020" />
        <display value="RETINAL CONE DYSTROPHY 1" />
      </concept>
      <concept>
        <code value="OMIM:180050" />
        <display value="RETINAL DETACHMENT" />
      </concept>
      <concept>
        <code value="OMIM:180080" />
        <display value="RETINAL VENOUS BEADING" />
      </concept>
      <concept>
        <code value="OMIM:180100" />
        <display value="RETINITIS PIGMENTOSA 1" />
      </concept>
      <concept>
        <code value="OMIM:180104" />
        <display value="RETINITIS PIGMENTOSA 9" />
      </concept>
      <concept>
        <code value="OMIM:180105" />
        <display value="RETINITIS PIGMENTOSA 10" />
      </concept>
      <concept>
        <code value="OMIM:180200" />
        <display value="RETINOBLASTOMA" />
      </concept>
      <concept>
        <code value="OMIM:180210" />
        <display value="RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:180270" />
        <display value="RETINOSCHISIS, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:180295" />
        <display value="RHABDOMYOSARCOMA, EMBRYONAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:180300" />
        <display value="RHEUMATOID ARTHRITIS" />
      </concept>
      <concept>
        <code value="OMIM:180350" />
        <display value="RHEUMATOID NODULOSIS" />
      </concept>
      <concept>
        <code value="OMIM:180360" />
        <display value="RHINY" />
      </concept>
      <concept>
        <code value="OMIM:180500" />
        <display value="AXENFELD-RIEGER SYNDROME, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:180550" />
        <display value="RING DERMOID OF CORNEA" />
      </concept>
      <concept>
        <code value="OMIM:180600" />
        <display value="RINGED HAIR" />
      </concept>
      <concept>
        <code value="OMIM:180700" />
        <display value="ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:180730" />
        <display value="ROMBO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:180750" />
        <display value="ROBINOW-SORAUF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:180800" />
        <display value="ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA" />
      </concept>
      <concept>
        <code value="OMIM:180849" />
        <display value="RUBINSTEIN-TAYBI SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:180860" />
        <display value="SILVER-RUSSELL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:180870" />
        <display value="RUVALCABA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:180900" />
        <display value="RUTHERFURD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:180920" />
        <display value="APLASIA OF LACRIMAL AND SALIVARY GLANDS" />
      </concept>
      <concept>
        <code value="OMIM:180950" />
        <display value="SALIVARY SUBSTANCE, CLOSTRIDIUM BOTULINUM TYPE" />
      </concept>
      <concept>
        <code value="OMIM:181000" />
        <display value="SARCOIDOSIS, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:181010" />
        <display value="SALIVARY DUCT CALCULI" />
      </concept>
      <concept>
        <code value="OMIM:181030" />
        <display value="SALIVARY GLAND ADENOMA, PLEOMORPHIC" />
      </concept>
      <concept>
        <code value="OMIM:181180" />
        <display value="SAY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:181200" />
        <display value="SC(1) TRAIT OF SALIVA" />
      </concept>
      <concept>
        <code value="OMIM:181250" />
        <display value="SCALP DEFECTS AND POSTAXIAL POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:181270" />
        <display value="SCALP-EAR-NIPPLE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:181300" />
        <display value="SCAPULA, CONTOUR OF VERTEBRAL BORDER OF" />
      </concept>
      <concept>
        <code value="OMIM:181350" />
        <display value="EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:181400" />
        <display value="SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:181405" />
        <display value="SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:181430" />
        <display value="SCAPULOPERONEAL MYOPATHY, MYH7-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:181440" />
        <display value="SCHEUERMANN DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:181450" />
        <display value="ULNAR-MAMMARY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:181460" />
        <display value="SCHISTOSOMA MANSONI INFECTION, SUSCEPTIBILITY/RESISTANCE TO" />
      </concept>
      <concept>
        <code value="OMIM:181500" />
        <display value="SCHIZOPHRENIA" />
      </concept>
      <concept>
        <code value="OMIM:181510" />
        <display value="SCHIZOPHRENIA 1" />
      </concept>
      <concept>
        <code value="OMIM:181600" />
        <display value="HURIEZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:181700" />
        <display value="SCLEROCORNEA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:181750" />
        <display value="SCLERODERMA, FAMILIAL PROGRESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:181800" />
        <display value="SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:182000" />
        <display value="KERATOSIS, SEBORRHEIC" />
      </concept>
      <concept>
        <code value="OMIM:182100" />
        <display value="FUCOSYLTRANSFERASE 2" />
      </concept>
      <concept>
        <code value="OMIM:182150" />
        <display value="SIMOSA CRANIOFACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:182170" />
        <display value="ANEMIA, SIDEROBLASTIC, 4" />
      </concept>
      <concept>
        <code value="OMIM:182190" />
        <display value="SINUS NODE DISEASE AND MYOPIA" />
      </concept>
      <concept>
        <code value="OMIM:182200" />
        <display value="SELLA TURCICA, BRIDGED" />
      </concept>
      <concept>
        <code value="OMIM:182210" />
        <display value="SHPRINTZEN OMPHALOCELE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:182212" />
        <display value="SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:182220" />
        <display value="SISTER CHROMATID EXCHANGE, FREQUENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:182230" />
        <display value="SEPTOOPTIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:182250" />
        <display value="SINGLETON-MERTEN SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:182255" />
        <display value="SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION" />
      </concept>
      <concept>
        <code value="OMIM:182260" />
        <display value="SLIPPED FEMORAL CAPITAL EPIPHYSES" />
      </concept>
      <concept>
        <code value="OMIM:182269" />
        <display value="SMALL PROLINE-RICH PROTEIN 2C, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:182270" />
        <display value="KETONE COMPOUNDS, ABILITY TO SMELL" />
      </concept>
      <concept>
        <code value="OMIM:182280" />
        <display value="SMALL CELL CANCER OF THE LUNG" />
      </concept>
      <concept>
        <code value="OMIM:182290" />
        <display value="SMITH-MAGENIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:182400" />
        <display value="SOMATOMEDIN, EMBRYONIC" />
      </concept>
      <concept>
        <code value="OMIM:182410" />
        <display value="SNEDDON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:182455" />
        <display value="SOMATOSTATIN RECEPTOR 5" />
      </concept>
      <concept>
        <code value="OMIM:182600" />
        <display value="SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:182601" />
        <display value="SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:182610" />
        <display value="SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:182690" />
        <display value="SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND PROGRESSIVE NEPHROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:182800" />
        <display value="SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS" />
      </concept>
      <concept>
        <code value="OMIM:182815" />
        <display value="SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA" />
      </concept>
      <concept>
        <code value="OMIM:182820" />
        <display value="SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY" />
      </concept>
      <concept>
        <code value="OMIM:182830" />
        <display value="SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:182875" />
        <display value="SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, AND TRANSVERSE EARLOBE CREASE" />
      </concept>
      <concept>
        <code value="OMIM:182882" />
        <display value="SPERM PROTAMINE P4" />
      </concept>
      <concept>
        <code value="OMIM:182900" />
        <display value="SPHEROCYTOSIS, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:182920" />
        <display value="MYOPATHY, SPHEROID BODY" />
      </concept>
      <concept>
        <code value="OMIM:182940" />
        <display value="NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:182950" />
        <display value="SPINAL ARACHNOIDITIS" />
      </concept>
      <concept>
        <code value="OMIM:182960" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:182970" />
        <display value="SPINAL MUSCULAR ATROPHY, FACIOSCAPULOHUMERAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:182980" />
        <display value="SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:182990" />
        <display value="SPINAL INTRADURAL ARACHNOID CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:183020" />
        <display value="SPINAL MUSCULAR ATROPHY, SEGMENTAL" />
      </concept>
      <concept>
        <code value="OMIM:183050" />
        <display value="SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:183086" />
        <display value="SPINOCEREBELLAR ATAXIA 6" />
      </concept>
      <concept>
        <code value="OMIM:183090" />
        <display value="SPINOCEREBELLAR ATAXIA 2" />
      </concept>
      <concept>
        <code value="OMIM:183100" />
        <display value="SPINOCEREBELLAR ATROPHY WITH PUPILLARY PARALYSIS" />
      </concept>
      <concept>
        <code value="OMIM:183300" />
        <display value="SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA" />
      </concept>
      <concept>
        <code value="OMIM:183350" />
        <display value="SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA AND REDUCED CIRCULATING T HELPER CELLS" />
      </concept>
      <concept>
        <code value="OMIM:183400" />
        <display value="SPLIT LOWER LIP" />
      </concept>
      <concept>
        <code value="OMIM:183500" />
        <display value="SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA" />
      </concept>
      <concept>
        <code value="OMIM:183600" />
        <display value="SPLIT-HAND/FOOT MALFORMATION 1" />
      </concept>
      <concept>
        <code value="OMIM:183700" />
        <display value="SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:183800" />
        <display value="SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS" />
      </concept>
      <concept>
        <code value="OMIM:183802" />
        <display value="SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATIC DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:183840" />
        <display value="SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:183849" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS" />
      </concept>
      <concept>
        <code value="OMIM:183850" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA WITH PUNCTATE CORNEAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:183900" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA" />
      </concept>
      <concept>
        <code value="OMIM:184000" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:184095" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE" />
      </concept>
      <concept>
        <code value="OMIM:184100" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:184200" />
        <display value="SPONDYLOLISTHESIS" />
      </concept>
      <concept>
        <code value="OMIM:184250" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE" />
      </concept>
      <concept>
        <code value="OMIM:184252" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:184253" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:184255" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:184260" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA" />
      </concept>
      <concept>
        <code value="OMIM:184300" />
        <display value="SPONDYLOSIS, CERVICAL" />
      </concept>
      <concept>
        <code value="OMIM:184400" />
        <display value="SPRENGEL DEFORMITY" />
      </concept>
      <concept>
        <code value="OMIM:184450" />
        <display value="STUTTERING, FAMILIAL PERSISTENT, 1" />
      </concept>
      <concept>
        <code value="OMIM:184460" />
        <display value="STAPES ANKYLOSIS WITH BROAD THUMBS AND TOES" />
      </concept>
      <concept>
        <code value="OMIM:184500" />
        <display value="STEATOCYSTOMA MULTIPLEX" />
      </concept>
      <concept>
        <code value="OMIM:184510" />
        <display value="STEATOCYSTOMA MULTIPLEX WITH NATAL TEETH" />
      </concept>
      <concept>
        <code value="OMIM:184700" />
        <display value="POLYCYSTIC OVARY SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:184705" />
        <display value="STEINFELD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:184800" />
        <display value="STERNUM, PREMATURE OBLITERATION OF SUTURES OF" />
      </concept>
      <concept>
        <code value="OMIM:184840" />
        <display value="OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:184850" />
        <display value="STIFF-PERSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:184900" />
        <display value="STIFF SKIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:185000" />
        <display value="OVERHYDRATED HEREDITARY STOMATOCYTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:185020" />
        <display value="CRYOHYDROCYTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:185050" />
        <display value="STORAGE POOL PLATELET DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:185069" />
        <display value="STORM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:185070" />
        <display value="STORMORKEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:185100" />
        <display value="STRABISMUS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:185120" />
        <display value="STRATTON-PARKER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:185200" />
        <display value="STRIAE DISTENSAE, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:185300" />
        <display value="STURGE-WEBER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:185460" />
        <display value="SULFHEMOGLOBINEMIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:185480" />
        <display value="SUPRABULBAR PARESIS, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:185500" />
        <display value="SUPRAVALVULAR AORTIC STENOSIS" />
      </concept>
      <concept>
        <code value="OMIM:185540" />
        <display value="SURFACE ANTIGEN, GLYCOPROTEIN 75" />
      </concept>
      <concept>
        <code value="OMIM:185600" />
        <display value="SYMPHALANGISM OF TOES" />
      </concept>
      <concept>
        <code value="OMIM:185610" />
        <display value="SURFACE POLYPEPTIDES, ANONYMOUS" />
      </concept>
      <concept>
        <code value="OMIM:185650" />
        <display value="SYMPHALANGISM, C. S. LEWIS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:185700" />
        <display value="SYMPHALANGISM, DISTAL" />
      </concept>
      <concept>
        <code value="OMIM:185750" />
        <display value="SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET" />
      </concept>
      <concept>
        <code value="OMIM:185800" />
        <display value="SYMPHALANGISM, PROXIMAL, 1A" />
      </concept>
      <concept>
        <code value="OMIM:185900" />
        <display value="CHROMOSOME 2q35 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:186000" />
        <display value="SYNPOLYDACTYLY 1" />
      </concept>
      <concept>
        <code value="OMIM:186100" />
        <display value="SYNDACTYLY, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:186200" />
        <display value="SYNDACTYLY, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:186300" />
        <display value="SYNDACTYLY, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:186350" />
        <display value="SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:186400" />
        <display value="SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL" />
      </concept>
      <concept>
        <code value="OMIM:186500" />
        <display value="MULTIPLE SYNOSTOSES SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:186550" />
        <display value="LIEBENBERG SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:186570" />
        <display value="TARSAL-CARPAL COALITION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:186575" />
        <display value="SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM" />
      </concept>
      <concept>
        <code value="OMIM:186580" />
        <display value="BLAU SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:186600" />
        <display value="SYRINGOMAS, MULTIPLE" />
      </concept>
      <concept>
        <code value="OMIM:186700" />
        <display value="SYRINGOMYELIA, NONCOMMUNICATING ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:186750" />
        <display value="TALONAVICULAR COALITION" />
      </concept>
      <concept>
        <code value="OMIM:186850" />
        <display value="TARSAL COALITION" />
      </concept>
      <concept>
        <code value="OMIM:186890" />
        <display value="TEAR PROTEIN, ANODAL" />
      </concept>
      <concept>
        <code value="OMIM:186950" />
        <display value="T-CELL SUBGROUPS, NON-HLA-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:187000" />
        <display value="TEETH, ODD SHAPES OF" />
      </concept>
      <concept>
        <code value="OMIM:187030" />
        <display value="T-COMPLEX LOCUS TCP10B" />
      </concept>
      <concept>
        <code value="OMIM:187050" />
        <display value="TEETH PRESENT AT BIRTH" />
      </concept>
      <concept>
        <code value="OMIM:187100" />
        <display value="TEETH, SUPERNUMERARY" />
      </concept>
      <concept>
        <code value="OMIM:187260" />
        <display value="TELANGIECTASIA, HEREDITARY BENIGN" />
      </concept>
      <concept>
        <code value="OMIM:187290" />
        <display value="TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, H142" />
      </concept>
      <concept>
        <code value="OMIM:187300" />
        <display value="TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:187310" />
        <display value="TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, K12" />
      </concept>
      <concept>
        <code value="OMIM:187320" />
        <display value="TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, ts13" />
      </concept>
      <concept>
        <code value="OMIM:187330" />
        <display value="TEMPERATURE SENSITIVITY COMPLEMENTATION, CELL CYCLE SPECIFIC, ts546" />
      </concept>
      <concept>
        <code value="OMIM:187340" />
        <display value="TEMPERATURE-SENSITIVE LETHAL MUTATION" />
      </concept>
      <concept>
        <code value="OMIM:187350" />
        <display value="TELECANTHUS" />
      </concept>
      <concept>
        <code value="OMIM:187360" />
        <display value="TEMPORAL ARTERITIS" />
      </concept>
      <concept>
        <code value="OMIM:187370" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 10" />
      </concept>
      <concept>
        <code value="OMIM:187390" />
        <display value="TENDONS, EXTENSOR, OF FINGERS, ANOMALOUS INSERTION OF" />
      </concept>
      <concept>
        <code value="OMIM:187395" />
        <display value="TERATOCARCINOMA-DERIVED GROWTH FACTOR 1" />
      </concept>
      <concept>
        <code value="OMIM:187400" />
        <display value="TESTICULAR TORSION" />
      </concept>
      <concept>
        <code value="OMIM:187500" />
        <display value="TETRALOGY OF FALLOT" />
      </concept>
      <concept>
        <code value="OMIM:187501" />
        <display value="TETRALOGY OF FALLOT AND GLAUCOMA" />
      </concept>
      <concept>
        <code value="OMIM:187510" />
        <display value="TETRAMELIC MONODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:187550" />
        <display value="THALASSEMIA, BETA+, SILENT ALLELE" />
      </concept>
      <concept>
        <code value="OMIM:187600" />
        <display value="THANATOPHORIC DYSPLASIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:187601" />
        <display value="THANATOPHORIC DYSPLASIA, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:187650" />
        <display value="THEOPHYLLINE BIOTRANSFORMATION" />
      </concept>
      <concept>
        <code value="OMIM:187750" />
        <display value="THORACIC DYSOSTOSIS, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:187760" />
        <display value="THORACOLARYNGOPELVIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:187770" />
        <display value="THORACOPELVIC DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:187800" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 16" />
      </concept>
      <concept>
        <code value="OMIM:187900" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 17" />
      </concept>
      <concept>
        <code value="OMIM:187940" />
        <display value="THROMBOCYTE B" />
      </concept>
      <concept>
        <code value="OMIM:187950" />
        <display value="THROMBOCYTHEMIA 1" />
      </concept>
      <concept>
        <code value="OMIM:188000" />
        <display value="THROMBOCYTOPENIA 2" />
      </concept>
      <concept>
        <code value="OMIM:188020" />
        <display value="THROMBOCYTOPENIA, CYCLIC" />
      </concept>
      <concept>
        <code value="OMIM:188025" />
        <display value="THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE" />
      </concept>
      <concept>
        <code value="OMIM:188030" />
        <display value="THROMBOCYTOPENIC PURPURA, AUTOIMMUNE" />
      </concept>
      <concept>
        <code value="OMIM:188050" />
        <display value="THROMBOPHILIA DUE TO THROMBIN DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:188055" />
        <display value="THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:188100" />
        <display value="THUMB DEFORMITY" />
      </concept>
      <concept>
        <code value="OMIM:188150" />
        <display value="THUMB DEFORMITY AND ALOPECIA" />
      </concept>
      <concept>
        <code value="OMIM:188201" />
        <display value="THUMBS, STIFF, WITH BRACHYDACTYLY TYPE A1 AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:188400" />
        <display value="DIGEORGE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:188455" />
        <display value="THYROGLOSSAL DUCT CYST, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:188470" />
        <display value="THYROID CANCER, NONMEDULLARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:188545" />
        <display value="THYROTROPIN-RELEASING HORMONE RECEPTOR" />
      </concept>
      <concept>
        <code value="OMIM:188550" />
        <display value="THYROID CANCER, NONMEDULLARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:188560" />
        <display value="THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:188570" />
        <display value="THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:188580" />
        <display value="THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:188700" />
        <display value="BLOUNT DISEASE, INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:188740" />
        <display value="TIBIA, HYPOPLASIA OR APLASIA OF, WITH POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:188800" />
        <display value="TIBIAL TORSION, BILATERAL MEDIAL" />
      </concept>
      <concept>
        <code value="OMIM:188850" />
        <display value="TL ANTIGEN" />
      </concept>
      <concept>
        <code value="OMIM:188890" />
        <display value="TOBACCO ADDICTION, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:189000" />
        <display value="TOE, FIFTH, NUMBER OF PHALANGES IN" />
      </concept>
      <concept>
        <code value="OMIM:189100" />
        <display value="TOE, MISSHAPEN" />
      </concept>
      <concept>
        <code value="OMIM:189150" />
        <display value="TOE, ROTATED FIFTH" />
      </concept>
      <concept>
        <code value="OMIM:189200" />
        <display value="TOES, RELATIVE LENGTH OF FIRST AND SECOND" />
      </concept>
      <concept>
        <code value="OMIM:189230" />
        <display value="TOES, SPACE BETWEEN FIRST AND SECOND" />
      </concept>
      <concept>
        <code value="OMIM:189300" />
        <display value="TONGUE CURLING, FOLDING, OR ROLLING" />
      </concept>
      <concept>
        <code value="OMIM:189490" />
        <display value="MALPOSITION OF TEETH WITH OR WITHOUT HYPODONTIA/OLIGODONTIA" />
      </concept>
      <concept>
        <code value="OMIM:189500" />
        <display value="WITKOP SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:189600" />
        <display value="TORTICOLLIS" />
      </concept>
      <concept>
        <code value="OMIM:189700" />
        <display value="TORUS PALATINUS AND TORUS MANDIBULARIS" />
      </concept>
      <concept>
        <code value="OMIM:189800" />
        <display value="PREECLAMPSIA/ECLAMPSIA 1" />
      </concept>
      <concept>
        <code value="OMIM:189960" />
        <display value="TRACHEOESOPHAGEAL FISTULA WITH OR WITHOUT ESOPHAGEAL ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:189961" />
        <display value="TRACHEOPATHIA OSTEOPLASTICA" />
      </concept>
      <concept>
        <code value="OMIM:190100" />
        <display value="GENIOSPASM 1" />
      </concept>
      <concept>
        <code value="OMIM:190200" />
        <display value="TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS" />
      </concept>
      <concept>
        <code value="OMIM:190300" />
        <display value="TREMOR, HEREDITARY ESSENTIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:190310" />
        <display value="TREMOR, NYSTAGMUS, AND DUODENAL ULCER" />
      </concept>
      <concept>
        <code value="OMIM:190320" />
        <display value="TRICHODENTOOSSEOUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:190330" />
        <display value="TRICHOMEGALY" />
      </concept>
      <concept>
        <code value="OMIM:190340" />
        <display value="DISCOID FIBROMAS, FAMILIAL MULTIPLE" />
      </concept>
      <concept>
        <code value="OMIM:190345" />
        <display value="TRICHOEPITHELIOMAS, MULTIPLE DESMOPLASTIC" />
      </concept>
      <concept>
        <code value="OMIM:190350" />
        <display value="TRICHORHINOPHALANGEAL SYNDROME, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:190351" />
        <display value="TRICHORHINOPHALANGEAL SYNDROME, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:190360" />
        <display value="TRICHODYSPLASIA-XERODERMA" />
      </concept>
      <concept>
        <code value="OMIM:190400" />
        <display value="TRIGEMINAL NEURALGIA" />
      </concept>
      <concept>
        <code value="OMIM:190410" />
        <display value="TRIGGER THUMB" />
      </concept>
      <concept>
        <code value="OMIM:190420" />
        <display value="TRIGLYCERIDE STORAGE DISEASE, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:190430" />
        <display value="TRIGLYCERIDE STORAGE DISEASE, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:190440" />
        <display value="TRIGONOCEPHALY 1" />
      </concept>
      <concept>
        <code value="OMIM:190445" />
        <display value="TRIIODOTHYRONINE RECEPTOR AUXILIARY PROTEIN" />
      </concept>
      <concept>
        <code value="OMIM:190500" />
        <display value="TRIPHALANGEAL THUMB WITH DOUBLE PHALANGES" />
      </concept>
      <concept>
        <code value="OMIM:190600" />
        <display value="TRIPHALANGEAL THUMB, NONOPPOSABLE" />
      </concept>
      <concept>
        <code value="OMIM:190650" />
        <display value="TRIPHALANGEAL THUMBS AND DISLOCATION OF PATELLA" />
      </concept>
      <concept>
        <code value="OMIM:190680" />
        <display value="TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:190685" />
        <display value="DOWN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:190800" />
        <display value="TRISTICHIASIS" />
      </concept>
      <concept>
        <code value="OMIM:190900" />
        <display value="TRITANOPIA" />
      </concept>
      <concept>
        <code value="OMIM:191000" />
        <display value="TROCHLEA OF THE HUMERUS, APLASIA OF" />
      </concept>
      <concept>
        <code value="OMIM:191100" />
        <display value="TUBEROUS SCLEROSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:191150" />
        <display value="TUFTSIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:191181" />
        <display value="SUPPRESSOR OF TUMORIGENICITY 3" />
      </concept>
      <concept>
        <code value="OMIM:191200" />
        <display value="TUNE DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:191250" />
        <display value="TWINNING DUE TO SUPERFETATION" />
      </concept>
      <concept>
        <code value="OMIM:191270" />
        <display value="TYROSINASE-LIKE" />
      </concept>
      <concept>
        <code value="OMIM:191390" />
        <display value="INFLAMMATORY BOWEL DISEASE 11" />
      </concept>
      <concept>
        <code value="OMIM:191400" />
        <display value="ULNA AND FIBULA, HYPOPLASIA OF" />
      </concept>
      <concept>
        <code value="OMIM:191420" />
        <display value="ULNA METAPHYSEAL DYSPLASIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:191440" />
        <display value="ULNAR HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:191480" />
        <display value="UNCOMBABLE HAIR SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:191482" />
        <display value="UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, AND BRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:191500" />
        <display value="UNDRITZ ANOMALY" />
      </concept>
      <concept>
        <code value="OMIM:191520" />
        <display value="UPINGTON DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:191530" />
        <display value="URATE-BINDING GLOBULIN, DECREASE IN" />
      </concept>
      <concept>
        <code value="OMIM:191540" />
        <display value="URATE OXIDASE, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:191550" />
        <display value="URETER, BIFID OR DOUBLE" />
      </concept>
      <concept>
        <code value="OMIM:191600" />
        <display value="URETER, CANCER OF" />
      </concept>
      <concept>
        <code value="OMIM:191650" />
        <display value="URETEROCELE" />
      </concept>
      <concept>
        <code value="OMIM:191700" />
        <display value="UROLITHIASIS, URIC ACID, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:191800" />
        <display value="URINARY BLADDER, ATONY OF" />
      </concept>
      <concept>
        <code value="OMIM:191830" />
        <display value="RENAL HYPODYSPLASIA/APLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:191850" />
        <display value="URTICARIA, AQUAGENIC" />
      </concept>
      <concept>
        <code value="OMIM:191900" />
        <display value="MUCKLE-WELLS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:191950" />
        <display value="URTICARIA, FAMILIAL LOCALIZED HEAT" />
      </concept>
      <concept>
        <code value="OMIM:192000" />
        <display value="UTERINE ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:192050" />
        <display value="UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:192100" />
        <display value="UVULA, BIFID" />
      </concept>
      <concept>
        <code value="OMIM:192200" />
        <display value="VARICOSE VEINS" />
      </concept>
      <concept>
        <code value="OMIM:192300" />
        <display value="VASCULAR HELIX OF UMBILICAL CORD" />
      </concept>
      <concept>
        <code value="OMIM:192310" />
        <display value="VASCULITIS, LYMPHOCYTIC, NODULAR" />
      </concept>
      <concept>
        <code value="OMIM:192315" />
        <display value="VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:192350" />
        <display value="VATER/VACTERL ASSOCIATION" />
      </concept>
      <concept>
        <code value="OMIM:192400" />
        <display value="VEINS, PATTERN OF, ON ANTERIOR THORAX" />
      </concept>
      <concept>
        <code value="OMIM:192430" />
        <display value="VELOCARDIOFACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:192445" />
        <display value="VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE" />
      </concept>
      <concept>
        <code value="OMIM:192500" />
        <display value="LONG QT SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:192600" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:192605" />
        <display value="VENTRICULAR TACHYCARDIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:192700" />
        <display value="VENULAR INSUFFICIENCY, SYSTEMIC" />
      </concept>
      <concept>
        <code value="OMIM:192800" />
        <display value="VERTEBRAL FUSION, POSTERIOR LUMBOSACRAL, WITH BLEPHAROPTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:192900" />
        <display value="VERTEBRAL HYPOPLASIA WITH LUMBAR KYPHOSIS" />
      </concept>
      <concept>
        <code value="OMIM:192950" />
        <display value="VERTICAL TALUS, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:193000" />
        <display value="VESICOURETERAL REFLUX 1" />
      </concept>
      <concept>
        <code value="OMIM:193003" />
        <display value="NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:193005" />
        <display value="VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:193007" />
        <display value="VERTIGO, BENIGN RECURRENT" />
      </concept>
      <concept>
        <code value="OMIM:193070" />
        <display value="VIRUS RD114 RNA COMPLEMENTARITY" />
      </concept>
      <concept>
        <code value="OMIM:193090" />
        <display value="TRANSCOBALAMIN I DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:193100" />
        <display value="HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:193200" />
        <display value="VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6" />
      </concept>
      <concept>
        <code value="OMIM:193220" />
        <display value="VITREORETINOCHOROIDOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:193230" />
        <display value="VITREORETINAL DEGENERATION, SNOWFLAKE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:193235" />
        <display value="VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY" />
      </concept>
      <concept>
        <code value="OMIM:193240" />
        <display value="VOCAL CORD PARALYSIS AND PTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:193250" />
        <display value="VOLVULUS OF MIDGUT" />
      </concept>
      <concept>
        <code value="OMIM:193300" />
        <display value="VON HIPPEL-LINDAU SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:193400" />
        <display value="VON WILLEBRAND DISEASE, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:193450" />
        <display value="VULVOVAGINITIS, ALLERGIC SEMINAL" />
      </concept>
      <concept>
        <code value="OMIM:193500" />
        <display value="WAARDENBURG SYNDROME, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:193510" />
        <display value="WAARDENBURG SYNDROME, TYPE 2A" />
      </concept>
      <concept>
        <code value="OMIM:193520" />
        <display value="WATSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:193530" />
        <display value="WEYERS ACROFACIAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:193670" />
        <display value="WHIM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:193700" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 2A" />
      </concept>
      <concept>
        <code value="OMIM:193900" />
        <display value="WHITE SPONGE NEVUS 1" />
      </concept>
      <concept>
        <code value="OMIM:194000" />
        <display value="WIDOW'S PEAK" />
      </concept>
      <concept>
        <code value="OMIM:194050" />
        <display value="WILLIAMS-BEUREN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:194070" />
        <display value="WILMS TUMOR 1" />
      </concept>
      <concept>
        <code value="OMIM:194071" />
        <display value="WILMS TUMOR 2" />
      </concept>
      <concept>
        <code value="OMIM:194072" />
        <display value="WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:194080" />
        <display value="DENYS-DRASH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:194090" />
        <display value="WILMS TUMOR 3" />
      </concept>
      <concept>
        <code value="OMIM:194190" />
        <display value="WOLF-HIRSCHHORN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:194200" />
        <display value="WOLFF-PARKINSON-WHITE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:194300" />
        <display value="WOOLLY HAIR, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:194320" />
        <display value="WORONETS TRAIT" />
      </concept>
      <concept>
        <code value="OMIM:194350" />
        <display value="WT LIMB-BLOOD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:194370" />
        <display value="X-RAY SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:194380" />
        <display value="DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA" />
      </concept>
      <concept>
        <code value="OMIM:194400" />
        <display value="XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD" />
      </concept>
      <concept>
        <code value="OMIM:194470" />
        <display value="ZINC, ELEVATED PLASMA" />
      </concept>
      <concept>
        <code value="OMIM:200100" />
        <display value="ABETALIPOPROTEINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:200110" />
        <display value="ABLEPHARON-MACROSTOMIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:200130" />
        <display value="ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:200150" />
        <display value="CHOREOACANTHOCYTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:200170" />
        <display value="ACANTHOSIS NIGRICANS WITH MUSCLE CRAMPS AND ACRAL ENLARGEMENT" />
      </concept>
      <concept>
        <code value="OMIM:200300" />
        <display value="ACETOPHENETIDIN SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:200400" />
        <display value="ACHALASIA, FAMILIAL ESOPHAGEAL" />
      </concept>
      <concept>
        <code value="OMIM:200450" />
        <display value="ACHALASIA-MICROCEPHALY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:200500" />
        <display value="ACHEIROPODY" />
      </concept>
      <concept>
        <code value="OMIM:200600" />
        <display value="ACHONDROGENESIS, TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:200610" />
        <display value="ACHONDROGENESIS, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:200700" />
        <display value="CHONDRODYSPLASIA, GREBE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:200900" />
        <display value="SHORT-LIMB SKELETAL DYSPLASIA WITH SEVERE COMBINED IMMUNODEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:200950" />
        <display value="ACID PHOSPHATASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:200970" />
        <display value="ACKERMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:200980" />
        <display value="ACRORENAL-MANDIBULAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:200990" />
        <display value="ACROCALLOSAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:200995" />
        <display value="ACROCEPHALOPOLYDACTYLOUS DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:201000" />
        <display value="CARPENTER SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:201020" />
        <display value="ACROCEPHALOPOLYSYNDACTYLY TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:201050" />
        <display value="ACROCRANIOFACIAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:201100" />
        <display value="ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:201170" />
        <display value="ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ" />
      </concept>
      <concept>
        <code value="OMIM:201180" />
        <display value="ACROFRONTOFACIONASAL DYSOSTOSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:201200" />
        <display value="ACROGERIA, GOTTRON TYPE" />
      </concept>
      <concept>
        <code value="OMIM:201250" />
        <display value="ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE" />
      </concept>
      <concept>
        <code value="OMIM:201300" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA" />
      </concept>
      <concept>
        <code value="OMIM:201310" />
        <display value="ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:201400" />
        <display value="ACTH DEFICIENCY, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:201450" />
        <display value="ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:201470" />
        <display value="ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:201475" />
        <display value="ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:201550" />
        <display value="ADDUCTED THUMBS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:201710" />
        <display value="LIPOID CONGENITAL ADRENAL HYPERPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:201750" />
        <display value="ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:201810" />
        <display value="ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:201910" />
        <display value="ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:202010" />
        <display value="ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:202110" />
        <display value="ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:202150" />
        <display value="ADRENAL HYPOPLASIA, CONGENITAL, WITH ABSENT PITUITARY LUTEINIZING HORMONE" />
      </concept>
      <concept>
        <code value="OMIM:202155" />
        <display value="ADRENAL HYPOPLASIA, CYTOMEGALIC TYPE" />
      </concept>
      <concept>
        <code value="OMIM:202200" />
        <display value="GLUCOCORTICOID DEFICIENCY 1" />
      </concept>
      <concept>
        <code value="OMIM:202300" />
        <display value="ADRENOCORTICAL CARCINOMA, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:202355" />
        <display value="ADRENOCORTICAL UNRESPONSIVENESS TO ACTH WITH POSTRECEPTOR DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:202370" />
        <display value="PEROXISOME BIOGENESIS DISORDER 2B" />
      </concept>
      <concept>
        <code value="OMIM:202400" />
        <display value="AFIBRINOGENEMIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:202550" />
        <display value="AGANGLIONOSIS, TOTAL INTESTINAL" />
      </concept>
      <concept>
        <code value="OMIM:202600" />
        <display value="AGENESIS OF CEREBRAL WHITE MATTER" />
      </concept>
      <concept>
        <code value="OMIM:202650" />
        <display value="AGNATHIA-OTOCEPHALY COMPLEX" />
      </concept>
      <concept>
        <code value="OMIM:202660" />
        <display value="PAGOD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:202700" />
        <display value="NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:202900" />
        <display value="ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETES MELLITUS" />
      </concept>
      <concept>
        <code value="OMIM:203000" />
        <display value="FRONTONASAL DYSPLASIA WITH ALAR CLEFTS" />
      </concept>
      <concept>
        <code value="OMIM:203100" />
        <display value="ALBINISM, OCULOCUTANEOUS, TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:203200" />
        <display value="ALBINISM, OCULOCUTANEOUS, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:203290" />
        <display value="ALBINISM, OCULOCUTANEOUS, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:203300" />
        <display value="HERMANSKY-PUDLAK SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:203330" />
        <display value="PSEUDOHYPOPARATHYROIDISM, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:203340" />
        <display value="ALBINISM-MICROCEPHALY-DIGITAL ANOMALIES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:203400" />
        <display value="CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:203450" />
        <display value="ALEXANDER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:203500" />
        <display value="ALKAPTONURIA" />
      </concept>
      <concept>
        <code value="OMIM:203550" />
        <display value="ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:203600" />
        <display value="ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN" />
      </concept>
      <concept>
        <code value="OMIM:203650" />
        <display value="ALOPECIA-MENTAL RETARDATION SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:203655" />
        <display value="ALOPECIA UNIVERSALIS CONGENITA" />
      </concept>
      <concept>
        <code value="OMIM:203700" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:203740" />
        <display value="ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:203750" />
        <display value="ALPHA-METHYLACETOACETIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:203760" />
        <display value="ALPHA-2-DEFICIENT COLLAGEN DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:203780" />
        <display value="ALPORT SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:203800" />
        <display value="ALSTROM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:204000" />
        <display value="LEBER CONGENITAL AMAUROSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:204100" />
        <display value="LEBER CONGENITAL AMAUROSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:204110" />
        <display value="AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS" />
      </concept>
      <concept>
        <code value="OMIM:204200" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:204300" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:204500" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:204650" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IC" />
      </concept>
      <concept>
        <code value="OMIM:204690" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IG" />
      </concept>
      <concept>
        <code value="OMIM:204700" />
        <display value="AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1" />
      </concept>
      <concept>
        <code value="OMIM:204730" />
        <display value="AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY, OSTEOPOROSIS, AND ACIDOSIS" />
      </concept>
      <concept>
        <code value="OMIM:204750" />
        <display value="2-AMINOADIPIC 2-OXOADIPIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:204800" />
        <display value="AMOBARBITAL, DEFICIENT N-HYDROXYLATION OF" />
      </concept>
      <concept>
        <code value="OMIM:204850" />
        <display value="AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:204870" />
        <display value="CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE" />
      </concept>
      <concept>
        <code value="OMIM:204900" />
        <display value="AMYLOIDOSIS, CUTANEOUS BULLOUS" />
      </concept>
      <concept>
        <code value="OMIM:205000" />
        <display value="AMYOTONIA CONGENITA" />
      </concept>
      <concept>
        <code value="OMIM:205100" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:205200" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:205250" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES" />
      </concept>
      <concept>
        <code value="OMIM:205400" />
        <display value="TANGIER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:205700" />
        <display value="ANEMIA, AUTOIMMUNE HEMOLYTIC" />
      </concept>
      <concept>
        <code value="OMIM:205950" />
        <display value="ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY" />
      </concept>
      <concept>
        <code value="OMIM:206000" />
        <display value="ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:206100" />
        <display value="ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1" />
      </concept>
      <concept>
        <code value="OMIM:206200" />
        <display value="IRON-REFRACTORY IRON DEFICIENCY ANEMIA" />
      </concept>
      <concept>
        <code value="OMIM:206300" />
        <display value="ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF RED CELL MEMBRANE" />
      </concept>
      <concept>
        <code value="OMIM:206400" />
        <display value="ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRIN METABOLISM" />
      </concept>
      <concept>
        <code value="OMIM:206500" />
        <display value="ANENCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:206550" />
        <display value="ANGIOLIPOMATOSIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:206570" />
        <display value="ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT" />
      </concept>
      <concept>
        <code value="OMIM:206600" />
        <display value="ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS" />
      </concept>
      <concept>
        <code value="OMIM:206700" />
        <display value="GILLESPIE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:206750" />
        <display value="ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTOR RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:206780" />
        <display value="ANODONTIA OF PERMANENT DENTITION" />
      </concept>
      <concept>
        <code value="OMIM:206800" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:206900" />
        <display value="MICROPHTHALMIA, SYNDROMIC 3" />
      </concept>
      <concept>
        <code value="OMIM:206920" />
        <display value="MICROPHTHALMIA WITH LIMB ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:207000" />
        <display value="ANOSMIA FOR ISOBUTYRIC ACID" />
      </concept>
      <concept>
        <code value="OMIM:207300" />
        <display value="ANTITHROMBIN, FAMILIAL HEMORRHAGIC DIATHESIS DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:207410" />
        <display value="ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:207500" />
        <display value="ANUS, IMPERFORATE" />
      </concept>
      <concept>
        <code value="OMIM:207600" />
        <display value="TAKAYASU ARTERITIS" />
      </concept>
      <concept>
        <code value="OMIM:207620" />
        <display value="APHALANGY WITH HEMIVERTEBRAE" />
      </concept>
      <concept>
        <code value="OMIM:207720" />
        <display value="APNEA, CENTRAL SLEEP" />
      </concept>
      <concept>
        <code value="OMIM:207731" />
        <display value="APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA" />
      </concept>
      <concept>
        <code value="OMIM:207740" />
        <display value="APLASIA OF EXTENSOR MUSCLES OF FINGERS, UNILATERAL, WITH GENERALIZED POLYNEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:207750" />
        <display value="APOLIPOPROTEIN C-II DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:207770" />
        <display value="APROSENCEPHALY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:207780" />
        <display value="AREDYLD" />
      </concept>
      <concept>
        <code value="OMIM:207790" />
        <display value="ARACHNOID CYSTS, INTRACRANIAL" />
      </concept>
      <concept>
        <code value="OMIM:207800" />
        <display value="ARGININEMIA" />
      </concept>
      <concept>
        <code value="OMIM:207900" />
        <display value="ARGININOSUCCINIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:207950" />
        <display value="CHIARI MALFORMATION TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:208000" />
        <display value="ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1" />
      </concept>
      <concept>
        <code value="OMIM:208050" />
        <display value="ARTERIAL TORTUOSITY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:208060" />
        <display value="ARTERIOSCLEROSIS, SEVERE JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:208080" />
        <display value="ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION, AND FACIAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:208081" />
        <display value="ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTIC FACIES" />
      </concept>
      <concept>
        <code value="OMIM:208085" />
        <display value="ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1" />
      </concept>
      <concept>
        <code value="OMIM:208100" />
        <display value="ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE" />
      </concept>
      <concept>
        <code value="OMIM:208150" />
        <display value="FETAL AKINESIA DEFORMATION SEQUENCE" />
      </concept>
      <concept>
        <code value="OMIM:208155" />
        <display value="ILLUM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:208158" />
        <display value="ARTHROGRYPOSIS WITH HYPERKERATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:208230" />
        <display value="ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD" />
      </concept>
      <concept>
        <code value="OMIM:208250" />
        <display value="CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:208300" />
        <display value="ASCITES, CHYLOUS" />
      </concept>
      <concept>
        <code value="OMIM:208400" />
        <display value="ASPARTYLGLUCOSAMINURIA" />
      </concept>
      <concept>
        <code value="OMIM:208500" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:208530" />
        <display value="RIGHT ATRIAL ISOMERISM" />
      </concept>
      <concept>
        <code value="OMIM:208540" />
        <display value="RENAL-HEPATIC-PANCREATIC DYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:208550" />
        <display value="ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE" />
      </concept>
      <concept>
        <code value="OMIM:208600" />
        <display value="ASTHMA, SHORT STATURE, AND ELEVATED IgA" />
      </concept>
      <concept>
        <code value="OMIM:208700" />
        <display value="ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:208750" />
        <display value="ATAXIA, DEAFNESS, AND CARDIOMYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:208850" />
        <display value="ATAXIA-DEAFNESS-RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:208870" />
        <display value="ATAXIA-MICROCEPHALY-CATARACT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:208900" />
        <display value="ATAXIA-TELANGIECTASIA" />
      </concept>
      <concept>
        <code value="OMIM:208910" />
        <display value="ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH" />
      </concept>
      <concept>
        <code value="OMIM:208920" />
        <display value="ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:209010" />
        <display value="ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS, PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:209050" />
        <display value="ATHROMBIA, ESSENTIAL" />
      </concept>
      <concept>
        <code value="OMIM:209100" />
        <display value="ATONIC-ASTATIC SYNDROME OF FOERSTER" />
      </concept>
      <concept>
        <code value="OMIM:209300" />
        <display value="ATRANSFERRINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:209500" />
        <display value="ATRICHIA WITH PAPULAR LESIONS" />
      </concept>
      <concept>
        <code value="OMIM:209600" />
        <display value="ATRIOVENTRICULAR DISSOCIATION" />
      </concept>
      <concept>
        <code value="OMIM:209700" />
        <display value="ATROPHODERMA VERMICULATA" />
      </concept>
      <concept>
        <code value="OMIM:209770" />
        <display value="AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:209800" />
        <display value="AUSTRALIA ANTIGEN" />
      </concept>
      <concept>
        <code value="OMIM:209850" />
        <display value="AUTISM" />
      </concept>
      <concept>
        <code value="OMIM:209880" />
        <display value="CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:209885" />
        <display value="BARBER-SAY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:209900" />
        <display value="BARDET-BIEDL SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:209920" />
        <display value="BARE LYMPHOCYTE SYNDROME, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:209950" />
        <display value="IMMUNODEFICIENCY 27A" />
      </concept>
      <concept>
        <code value="OMIM:209970" />
        <display value="BEEMER LETHAL MALFORMATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:210000" />
        <display value="BEHR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:210050" />
        <display value="BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION" />
      </concept>
      <concept>
        <code value="OMIM:210100" />
        <display value="BETA-AMINOISOBUTYRIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:210200" />
        <display value="3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:210210" />
        <display value="3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:210250" />
        <display value="SITOSTEROLEMIA" />
      </concept>
      <concept>
        <code value="OMIM:210350" />
        <display value="BIEMOND SYNDROME II" />
      </concept>
      <concept>
        <code value="OMIM:210370" />
        <display value="BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:210400" />
        <display value="BIFID NOSE, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:210500" />
        <display value="BILIARY ATRESIA, EXTRAHEPATIC" />
      </concept>
      <concept>
        <code value="OMIM:210550" />
        <display value="BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:210600" />
        <display value="SECKEL SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:210700" />
        <display value="MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:210710" />
        <display value="MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:210720" />
        <display value="MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:210730" />
        <display value="MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:210740" />
        <display value="BANGSTAD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:210745" />
        <display value="BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE" />
      </concept>
      <concept>
        <code value="OMIM:210750" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 6" />
      </concept>
      <concept>
        <code value="OMIM:210900" />
        <display value="BLOOM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:211000" />
        <display value="BLUE DIAPER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:211120" />
        <display value="BONE DYSPLASIA, LETHAL, HOLMGREN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:211180" />
        <display value="BOWEN-CONRADI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:211200" />
        <display value="BOWEN SYNDROME OF MULTIPLE MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:211350" />
        <display value="KYPHOMELIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:211355" />
        <display value="BOWING OF LONG BONES, ASYMMETRIC AND SYMMETRIC" />
      </concept>
      <concept>
        <code value="OMIM:211369" />
        <display value="BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:211370" />
        <display value="BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM" />
      </concept>
      <concept>
        <code value="OMIM:211380" />
        <display value="ELSAHY-WATERS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:211390" />
        <display value="SABINAS BRITTLE HAIR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:211400" />
        <display value="BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1" />
      </concept>
      <concept>
        <code value="OMIM:211450" />
        <display value="BRONCHOMALACIA" />
      </concept>
      <concept>
        <code value="OMIM:211480" />
        <display value="BUERGER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:211500" />
        <display value="FAZIO-LONDE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:211530" />
        <display value="BROWN-VIALETTO-VAN LAERE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:211600" />
        <display value="CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:211750" />
        <display value="C SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:211770" />
        <display value="CAHMR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:211800" />
        <display value="CALCIFICATION OF JOINTS AND ARTERIES" />
      </concept>
      <concept>
        <code value="OMIM:211890" />
        <display value="CAMPOMELIA, CUMMING TYPE" />
      </concept>
      <concept>
        <code value="OMIM:211900" />
        <display value="TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:211910" />
        <display value="CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:211920" />
        <display value="CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:211930" />
        <display value="CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:211960" />
        <display value="CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMAL PALMAR CREASES" />
      </concept>
      <concept>
        <code value="OMIM:211965" />
        <display value="CAMPTODACTYLY-ICHTHYOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:211980" />
        <display value="LUNG CANCER" />
      </concept>
      <concept>
        <code value="OMIM:211990" />
        <display value="CAMPTOMELIC SYNDROME, LONG-LIMB TYPE" />
      </concept>
      <concept>
        <code value="OMIM:212050" />
        <display value="CANDIDIASIS, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:212060" />
        <display value="CARBIMAZOLE SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:212065" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia" />
      </concept>
      <concept>
        <code value="OMIM:212066" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa" />
      </concept>
      <concept>
        <code value="OMIM:212067" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx" />
      </concept>
      <concept>
        <code value="OMIM:212070" />
        <display value="CARBOXYPEPTIDASE N DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:212080" />
        <display value="CARDIAC LIPIDOSIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:212090" />
        <display value="CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA" />
      </concept>
      <concept>
        <code value="OMIM:212093" />
        <display value="CARDIAC VALVULAR DEFECT, DEVELOPMENTAL" />
      </concept>
      <concept>
        <code value="OMIM:212100" />
        <display value="CARDIOAUDITORY SYNDROME OF SANCHEZ CASCOS" />
      </concept>
      <concept>
        <code value="OMIM:212112" />
        <display value="CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:212130" />
        <display value="CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH" />
      </concept>
      <concept>
        <code value="OMIM:212135" />
        <display value="CARDIOSKELETAL SYNDROME, KUWAITI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:212138" />
        <display value="CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:212140" />
        <display value="CARNITINE DEFICIENCY, SYSTEMIC PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:212160" />
        <display value="CARNITINE DEFICIENCY, MYOPATHIC" />
      </concept>
      <concept>
        <code value="OMIM:212200" />
        <display value="CARNOSINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:212350" />
        <display value="SENGERS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:212360" />
        <display value="PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2" />
      </concept>
      <concept>
        <code value="OMIM:212400" />
        <display value="CATARACT AND CONGENITAL ICHTHYOSIS" />
      </concept>
      <concept>
        <code value="OMIM:212500" />
        <display value="CATARACT 46, JUVENILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:212540" />
        <display value="CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:212550" />
        <display value="OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:212710" />
        <display value="CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:212720" />
        <display value="MARTSOLF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:212750" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:212780" />
        <display value="CENANI-LENZ SYNDACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:212790" />
        <display value="PREMATURE CENTROMERE DIVISION" />
      </concept>
      <concept>
        <code value="OMIM:212800" />
        <display value="CEPHALIN LIPIDOSIS" />
      </concept>
      <concept>
        <code value="OMIM:212835" />
        <display value="CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:212840" />
        <display value="GORDON HOLMES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:212850" />
        <display value="CEREBELLAR ATAXIA AND NEUROSENSORY DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:212890" />
        <display value="CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA" />
      </concept>
      <concept>
        <code value="OMIM:212895" />
        <display value="CEREBELLAR ATAXIA, EARLY-ONSET, WITH RETAINED TENDON REFLEXES" />
      </concept>
      <concept>
        <code value="OMIM:213000" />
        <display value="CEREBELLAR HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:213002" />
        <display value="CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS" />
      </concept>
      <concept>
        <code value="OMIM:213010" />
        <display value="CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZ SYNDROME AND MECKEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:213100" />
        <display value="CEREBELLOPARENCHYMAL DISORDER II" />
      </concept>
      <concept>
        <code value="OMIM:213200" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:213300" />
        <display value="JOUBERT SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:213400" />
        <display value="CEREBELLOPARENCHYMAL DISORDER V" />
      </concept>
      <concept>
        <code value="OMIM:213500" />
        <display value="CEREBRAL ANGIOPATHY, DYSPHORIC" />
      </concept>
      <concept>
        <code value="OMIM:213600" />
        <display value="BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:213700" />
        <display value="CEREBROTENDINOUS XANTHOMATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:213820" />
        <display value="CEREBRAL MALFORMATION, SEIZURES, HYPERTRICHOSIS, AND OVERLAPPING FINGERS" />
      </concept>
      <concept>
        <code value="OMIM:213900" />
        <display value="CEREBRAL SCLEROSIS SIMILAR TO PELIZAEUS-MERZBACHER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:213950" />
        <display value="CEREBROCORTICAL DEGENERATION OF INFANCY" />
      </concept>
      <concept>
        <code value="OMIM:213980" />
        <display value="CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:214100" />
        <display value="PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:214110" />
        <display value="PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:214150" />
        <display value="CEREBROOCULOFACIOSKELETAL SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:214200" />
        <display value="CEROID STORAGE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:214290" />
        <display value="CERVICAL VERTEBRAE, AGENESIS OF" />
      </concept>
      <concept>
        <code value="OMIM:214300" />
        <display value="KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:214350" />
        <display value="CHAND SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:214370" />
        <display value="NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION, AND ABSENT SENSORY LARGE MYELINATED FIBERS" />
      </concept>
      <concept>
        <code value="OMIM:214400" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A" />
      </concept>
      <concept>
        <code value="OMIM:214450" />
        <display value="GRISCELLI SYNDROME, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:214500" />
        <display value="CHEDIAK-HIGASHI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:214700" />
        <display value="DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:214800" />
        <display value="CHARGE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:214900" />
        <display value="CHOLESTASIS-LYMPHEDEMA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:214950" />
        <display value="BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:214980" />
        <display value="CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE" />
      </concept>
      <concept>
        <code value="OMIM:215030" />
        <display value="CHOLESTEROL PNEUMONIA" />
      </concept>
      <concept>
        <code value="OMIM:215045" />
        <display value="CHONDRODYSPLASIA, BLOMSTRAND TYPE" />
      </concept>
      <concept>
        <code value="OMIM:215050" />
        <display value="CHONDRODYSPLASIA CALCIFICANS METAPHYSEALIS" />
      </concept>
      <concept>
        <code value="OMIM:215100" />
        <display value="RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:215105" />
        <display value="CHONDRODYSPLASIA PUNCTATA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:215140" />
        <display value="GREENBERG DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:215150" />
        <display value="OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:215250" />
        <display value="CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:215300" />
        <display value="CHONDROSARCOMA" />
      </concept>
      <concept>
        <code value="OMIM:215400" />
        <display value="CHORDOMA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:215450" />
        <display value="CHOREA, BENIGN FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:215470" />
        <display value="BOUCHER-NEUHAUSER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:215480" />
        <display value="CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:215500" />
        <display value="CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, 1" />
      </concept>
      <concept>
        <code value="OMIM:215510" />
        <display value="CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:215518" />
        <display value="CILIARY DISCOORDINATION DUE TO RANDOM CILIARY ORIENTATION" />
      </concept>
      <concept>
        <code value="OMIM:215520" />
        <display value="CILIARY DYSKINESIA WITH TRANSPOSITION OF CILIARY MICROTUBULES" />
      </concept>
      <concept>
        <code value="OMIM:215550" />
        <display value="CIRCUMVALLATE PLACENTA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:215600" />
        <display value="CIRRHOSIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:215700" />
        <display value="CITRULLINEMIA, CLASSIC" />
      </concept>
      <concept>
        <code value="OMIM:215720" />
        <display value="CITRULLINE TRANSPORT DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:215800" />
        <display value="CLEFT LARYNX, POSTERIOR" />
      </concept>
      <concept>
        <code value="OMIM:215850" />
        <display value="CLEFT-LIMB-HEART MALFORMATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:216100" />
        <display value="CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:216300" />
        <display value="CLEFT PALATE, DEAFNESS, AND OLIGODONTIA" />
      </concept>
      <concept>
        <code value="OMIM:216330" />
        <display value="CLEIDOCRANIAL DYSPLASIA, RECESSIVE FORM" />
      </concept>
      <concept>
        <code value="OMIM:216340" />
        <display value="YUNIS-VARON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:216360" />
        <display value="COACH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:216400" />
        <display value="COCKAYNE SYNDROME A" />
      </concept>
      <concept>
        <code value="OMIM:216550" />
        <display value="COHEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:216700" />
        <display value="COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING" />
      </concept>
      <concept>
        <code value="OMIM:216800" />
        <display value="COLOBOMA OF MACULA AND SKELETAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:216820" />
        <display value="COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:216900" />
        <display value="ACHROMATOPSIA 2" />
      </concept>
      <concept>
        <code value="OMIM:216920" />
        <display value="COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:216950" />
        <display value="COMPLEMENT COMPONENT C1r/C1s DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:217000" />
        <display value="COMPLEMENT COMPONENT 2 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:217080" />
        <display value="JALILI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:217085" />
        <display value="CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:217090" />
        <display value="PLASMINOGEN DEFICIENCY, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:217095" />
        <display value="CONOTRUNCAL HEART MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:217100" />
        <display value="CONSTRICTING BANDS, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:217150" />
        <display value="CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA" />
      </concept>
      <concept>
        <code value="OMIM:217200" />
        <display value="CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET" />
      </concept>
      <concept>
        <code value="OMIM:217300" />
        <display value="CORNEA PLANA 2, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:217400" />
        <display value="CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:217500" />
        <display value="CORNEAL DYSTROPHY, BAND-SHAPED" />
      </concept>
      <concept>
        <code value="OMIM:217520" />
        <display value="CORNEAL DEGENERATION, BAND-SHAPED SPHEROID" />
      </concept>
      <concept>
        <code value="OMIM:217600" />
        <display value="CENTRAL CLOUDY DYSTROPHY OF FRANCOIS" />
      </concept>
      <concept>
        <code value="OMIM:217700" />
        <display value="CORNEAL ENDOTHELIAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:217800" />
        <display value="MACULAR DYSTROPHY, CORNEAL" />
      </concept>
      <concept>
        <code value="OMIM:217980" />
        <display value="CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE" />
      </concept>
      <concept>
        <code value="OMIM:217990" />
        <display value="CORPUS CALLOSUM, AGENESIS OF" />
      </concept>
      <concept>
        <code value="OMIM:218000" />
        <display value="AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:218010" />
        <display value="CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:218030" />
        <display value="APPARENT MINERALOCORTICOID EXCESS" />
      </concept>
      <concept>
        <code value="OMIM:218040" />
        <display value="COSTELLO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:218050" />
        <display value="CRAMPS, FAMILIAL ADOLESCENT" />
      </concept>
      <concept>
        <code value="OMIM:218090" />
        <display value="CRANE-HEISE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:218100" />
        <display value="CRANIAL NERVES, CONGENITAL PARESIS OF" />
      </concept>
      <concept>
        <code value="OMIM:218200" />
        <display value="CRANIAL NERVES, RECURRENT PARESIS OF" />
      </concept>
      <concept>
        <code value="OMIM:218300" />
        <display value="CRANIODIAPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:218330" />
        <display value="CRANIOECTODERMAL DYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:218340" />
        <display value="TEMTAMY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:218350" />
        <display value="CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE" />
      </concept>
      <concept>
        <code value="OMIM:218400" />
        <display value="CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:218450" />
        <display value="CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS" />
      </concept>
      <concept>
        <code value="OMIM:218530" />
        <display value="CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS" />
      </concept>
      <concept>
        <code value="OMIM:218550" />
        <display value="CRANIOSYNOSTOSIS WITH FIBULAR APLASIA" />
      </concept>
      <concept>
        <code value="OMIM:218600" />
        <display value="BALLER-GEROLD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:218649" />
        <display value="CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG" />
      </concept>
      <concept>
        <code value="OMIM:218650" />
        <display value="CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:218670" />
        <display value="CRANIOTELENCEPHALIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:218700" />
        <display value="HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2" />
      </concept>
      <concept>
        <code value="OMIM:218800" />
        <display value="CRIGLER-NAJJAR SYNDROME, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:218900" />
        <display value="CROME SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:219000" />
        <display value="FRASER SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:219050" />
        <display value="CRYPTORCHIDISM, UNILATERAL OR BILATERAL" />
      </concept>
      <concept>
        <code value="OMIM:219070" />
        <display value="CURVED NAIL OF FOURTH TOE" />
      </concept>
      <concept>
        <code value="OMIM:219080" />
        <display value="ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:219090" />
        <display value="PITUITARY ADENOMA 4, ACTH-SECRETING" />
      </concept>
      <concept>
        <code value="OMIM:219095" />
        <display value="CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:219100" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:219150" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA" />
      </concept>
      <concept>
        <code value="OMIM:219200" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA" />
      </concept>
      <concept>
        <code value="OMIM:219250" />
        <display value="CUTIS MARMORATA TELANGIECTATICA CONGENITA" />
      </concept>
      <concept>
        <code value="OMIM:219300" />
        <display value="CUTIS VERTICIS GYRATA AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:219400" />
        <display value="CYANOSIS AND HEPATIC DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:219500" />
        <display value="CYSTATHIONINURIA" />
      </concept>
      <concept>
        <code value="OMIM:219550" />
        <display value="CYSTEINE PEPTIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:219600" />
        <display value="CYSTIC DISEASE OF LUNG" />
      </concept>
      <concept>
        <code value="OMIM:219700" />
        <display value="CYSTIC FIBROSIS" />
      </concept>
      <concept>
        <code value="OMIM:219721" />
        <display value="CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:219730" />
        <display value="VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:219750" />
        <display value="CYSTINOSIS, ADULT NONNEPHROPATHIC" />
      </concept>
      <concept>
        <code value="OMIM:219800" />
        <display value="CYSTINOSIS, NEPHROPATHIC" />
      </concept>
      <concept>
        <code value="OMIM:219900" />
        <display value="CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE" />
      </concept>
      <concept>
        <code value="OMIM:220100" />
        <display value="CYSTINURIA" />
      </concept>
      <concept>
        <code value="OMIM:220110" />
        <display value="MITOCHONDRIAL COMPLEX IV DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:220111" />
        <display value="LEIGH SYNDROME, FRENCH CANADIAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:220120" />
        <display value="D-GLYCERIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:220150" />
        <display value="HYPOURICEMIA, RENAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:220200" />
        <display value="DANDY-WALKER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:220210" />
        <display value="RITSCHER-SCHINZEL SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:220219" />
        <display value="DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY" />
      </concept>
      <concept>
        <code value="OMIM:220220" />
        <display value="DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:220290" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 1A" />
      </concept>
      <concept>
        <code value="OMIM:220300" />
        <display value="DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY" />
      </concept>
      <concept>
        <code value="OMIM:220400" />
        <display value="JERVELL AND LANGE-NIELSEN SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:220500" />
        <display value="DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:220600" />
        <display value="SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:220900" />
        <display value="DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM" />
      </concept>
      <concept>
        <code value="OMIM:221200" />
        <display value="DEAFNESS AND MYOPIA" />
      </concept>
      <concept>
        <code value="OMIM:221300" />
        <display value="DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR" />
      </concept>
      <concept>
        <code value="OMIM:221320" />
        <display value="DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:221350" />
        <display value="DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA" />
      </concept>
      <concept>
        <code value="OMIM:221400" />
        <display value="DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL AND PROGRESSIVE SENSORY NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:221500" />
        <display value="DEAFNESS, NEURAL, CONGENITAL MODERATE" />
      </concept>
      <concept>
        <code value="OMIM:221700" />
        <display value="DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS" />
      </concept>
      <concept>
        <code value="OMIM:221740" />
        <display value="DEAFNESS-OLIGODONTIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:221745" />
        <display value="DEAFNESS, SENSORINEURAL, AUTOSOMAL-MITOCHONDRIAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:221750" />
        <display value="PITUITARY HORMONE DEFICIENCY, COMBINED, 3" />
      </concept>
      <concept>
        <code value="OMIM:221760" />
        <display value="DERMATOGLYPHICS--PALMAR TRIRADIUS d, ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:221770" />
        <display value="POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 1" />
      </concept>
      <concept>
        <code value="OMIM:221780" />
        <display value="DERMATOGLYPHICS--HYPOTHENAR RADIAL ARCH" />
      </concept>
      <concept>
        <code value="OMIM:221790" />
        <display value="DERMATOLEUKODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:221800" />
        <display value="DERMOCHONDROCORNEAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:221810" />
        <display value="DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:221820" />
        <display value="LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS" />
      </concept>
      <concept>
        <code value="OMIM:221900" />
        <display value="PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:221950" />
        <display value="DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA" />
      </concept>
      <concept>
        <code value="OMIM:221995" />
        <display value="DIABETES INSIPIDUS, NEPHROGENIC, WITH MENTAL RETARDATION AND INTRACEREBRAL CALCIFICATION" />
      </concept>
      <concept>
        <code value="OMIM:222100" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT" />
      </concept>
      <concept>
        <code value="OMIM:222300" />
        <display value="WOLFRAM SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:222350" />
        <display value="DIAMINOPENTANURIA" />
      </concept>
      <concept>
        <code value="OMIM:222400" />
        <display value="DIAPHRAGMATIC HERNIA 2" />
      </concept>
      <concept>
        <code value="OMIM:222448" />
        <display value="DONNAI-BARROW SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:222470" />
        <display value="TRICHOHEPATOENTERIC SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:222500" />
        <display value="DIASTEMATOMYELIA" />
      </concept>
      <concept>
        <code value="OMIM:222600" />
        <display value="DIASTROPHIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:222690" />
        <display value="DIBASIC AMINO ACIDURIA I" />
      </concept>
      <concept>
        <code value="OMIM:222700" />
        <display value="LYSINURIC PROTEIN INTOLERANCE" />
      </concept>
      <concept>
        <code value="OMIM:222730" />
        <display value="DICARBOXYLIC AMINOACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:222748" />
        <display value="DIHYDROPYRIMIDINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:222765" />
        <display value="RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:222800" />
        <display value="BISPHOSPHOGLYCERATE MUTASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:222900" />
        <display value="SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:223000" />
        <display value="LACTASE DEFICIENCY, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:223100" />
        <display value="LACTOSE INTOLERANCE, ADULT TYPE" />
      </concept>
      <concept>
        <code value="OMIM:223200" />
        <display value="DISORGANIZATION, MOUSE, HOMOLOG OF" />
      </concept>
      <concept>
        <code value="OMIM:223300" />
        <display value="DISSEMINATED SCLEROSIS WITH NARCOLEPSY" />
      </concept>
      <concept>
        <code value="OMIM:223320" />
        <display value="DIVERTICULOSIS, SMALL-INTESTINAL" />
      </concept>
      <concept>
        <code value="OMIM:223330" />
        <display value="DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT" />
      </concept>
      <concept>
        <code value="OMIM:223340" />
        <display value="DK PHOCOMELIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:223350" />
        <display value="DOHLE BODIES AND LEUKEMIA" />
      </concept>
      <concept>
        <code value="OMIM:223360" />
        <display value="ORTHOSTATIC HYPOTENSION 1" />
      </concept>
      <concept>
        <code value="OMIM:223370" />
        <display value="DUBOWITZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:223380" />
        <display value="DOPAMINE BETA-HYDROXYLASE, PLASMA, THERMOLABILITY OF" />
      </concept>
      <concept>
        <code value="OMIM:223400" />
        <display value="DUODENAL ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:223500" />
        <display value="DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE" />
      </concept>
      <concept>
        <code value="OMIM:223540" />
        <display value="DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY" />
      </concept>
      <concept>
        <code value="OMIM:223550" />
        <display value="DWARFISM, PROPORTIONATE, WITH HIP DISLOCATION" />
      </concept>
      <concept>
        <code value="OMIM:223800" />
        <display value="DYGGVE-MELCHIOR-CLAUSEN DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:223900" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:224000" />
        <display value="DYSAUTONOMIA-LIKE DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:224050" />
        <display value="CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:224100" />
        <display value="ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:224120" />
        <display value="ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia" />
      </concept>
      <concept>
        <code value="OMIM:224230" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1" />
      </concept>
      <concept>
        <code value="OMIM:224250" />
        <display value="DYSMYELINATION WITH JAUNDICE" />
      </concept>
      <concept>
        <code value="OMIM:224300" />
        <display value="DYSOSTEOSCLEROSIS" />
      </concept>
      <concept>
        <code value="OMIM:224400" />
        <display value="DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:224410" />
        <display value="DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:224500" />
        <display value="DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:224550" />
        <display value="DYSTONIA WITH RINGBINDEN" />
      </concept>
      <concept>
        <code value="OMIM:224690" />
        <display value="MEIER-GORLIN SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:224700" />
        <display value="EBSTEIN ANOMALY" />
      </concept>
      <concept>
        <code value="OMIM:224750" />
        <display value="SCHOPF-SCHULZ-PASSARGE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:224800" />
        <display value="ECTODERMAL DYSPLASIA AND NEUROSENSORY DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:224900" />
        <display value="ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:225000" />
        <display value="ROSSELLI-GULIENETTI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:225040" />
        <display value="ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESIS OF THE CORPUS CALLOSUM" />
      </concept>
      <concept>
        <code value="OMIM:225050" />
        <display value="ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARY DYSKINESIA" />
      </concept>
      <concept>
        <code value="OMIM:225060" />
        <display value="CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:225100" />
        <display value="ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:225200" />
        <display value="ECTOPIA LENTIS ET PUPILLAE" />
      </concept>
      <concept>
        <code value="OMIM:225250" />
        <display value="HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5" />
      </concept>
      <concept>
        <code value="OMIM:225280" />
        <display value="ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:225290" />
        <display value="ECTRODACTYLY-POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:225300" />
        <display value="SPLIT-HAND/FOOT MALFORMATION 6" />
      </concept>
      <concept>
        <code value="OMIM:225310" />
        <display value="EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTIN ABNORMALITY" />
      </concept>
      <concept>
        <code value="OMIM:225320" />
        <display value="EHLERS-DANLOS SYNDROME, CARDIAC VALVULAR TYPE" />
      </concept>
      <concept>
        <code value="OMIM:225400" />
        <display value="EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 1" />
      </concept>
      <concept>
        <code value="OMIM:225410" />
        <display value="EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:225500" />
        <display value="ELLIS-VAN CREVELD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:225700" />
        <display value="ENCEPHALOMALACIA, MULTILOCULAR" />
      </concept>
      <concept>
        <code value="OMIM:225740" />
        <display value="ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS" />
      </concept>
      <concept>
        <code value="OMIM:225750" />
        <display value="AICARDI-GOUTIERES SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:225753" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:225755" />
        <display value="ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:225790" />
        <display value="PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:226000" />
        <display value="ENDOCARDIAL FIBROELASTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:226100" />
        <display value="ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA" />
      </concept>
      <concept>
        <code value="OMIM:226110" />
        <display value="ENDOTHELIAL DYSTROPHY, CONGENITAL HEREDITARY, WITH NAIL HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:226150" />
        <display value="ENTEROCOLITIS" />
      </concept>
      <concept>
        <code value="OMIM:226200" />
        <display value="ENTEROKINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:226300" />
        <display value="COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:226350" />
        <display value="EOSINOPHILIC FASCIITIS" />
      </concept>
      <concept>
        <code value="OMIM:226400" />
        <display value="EPIDERMODYSPLASIA VERRUCIFORMIS" />
      </concept>
      <concept>
        <code value="OMIM:226440" />
        <display value="EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:226500" />
        <display value="EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA" />
      </concept>
      <concept>
        <code value="OMIM:226600" />
        <display value="EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:226650" />
        <display value="EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE" />
      </concept>
      <concept>
        <code value="OMIM:226670" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:226700" />
        <display value="EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE" />
      </concept>
      <concept>
        <code value="OMIM:226730" />
        <display value="EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:226735" />
        <display value="EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA" />
      </concept>
      <concept>
        <code value="OMIM:226750" />
        <display value="KOHLSCHUTTER-TONZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:226800" />
        <display value="EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:226810" />
        <display value="EPILEPSY WITH BILATERAL OCCIPITAL CALCIFICATIONS" />
      </concept>
      <concept>
        <code value="OMIM:226850" />
        <display value="EPILEPSY-TELANGIECTASIA" />
      </concept>
      <concept>
        <code value="OMIM:226900" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, 4" />
      </concept>
      <concept>
        <code value="OMIM:226950" />
        <display value="EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:226960" />
        <display value="EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS" />
      </concept>
      <concept>
        <code value="OMIM:226980" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS" />
      </concept>
      <concept>
        <code value="OMIM:226985" />
        <display value="EPITHELIAL SQUAMOUS DYSPLASIA, KERATINIZING DESQUAMATIVE, OF URINARY TRACT" />
      </concept>
      <concept>
        <code value="OMIM:226990" />
        <display value="IMMUNODEFICIENCY 32B" />
      </concept>
      <concept>
        <code value="OMIM:227000" />
        <display value="ERYTHEMA OF ACRAL REGIONS" />
      </concept>
      <concept>
        <code value="OMIM:227010" />
        <display value="ERMINE PHENOTYPE" />
      </concept>
      <concept>
        <code value="OMIM:227050" />
        <display value="TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD" />
      </concept>
      <concept>
        <code value="OMIM:227090" />
        <display value="ERYTHRODERMA, LETHAL CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:227150" />
        <display value="ETHANOLAMINOSIS" />
      </concept>
      <concept>
        <code value="OMIM:227210" />
        <display value="EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:227220" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1" />
      </concept>
      <concept>
        <code value="OMIM:227240" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5" />
      </concept>
      <concept>
        <code value="OMIM:227250" />
        <display value="FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:227255" />
        <display value="FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:227260" />
        <display value="FOCAL FACIAL DERMAL DYSPLASIA 3, SETLEIS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:227270" />
        <display value="FACIOCARDIOMELIC DYSPLASIA, LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:227280" />
        <display value="FACIOCARDIORENAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:227300" />
        <display value="FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1" />
      </concept>
      <concept>
        <code value="OMIM:227310" />
        <display value="FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEIN C AND PROTEIN C INHIBITOR" />
      </concept>
      <concept>
        <code value="OMIM:227320" />
        <display value="FACIOTHORACOGENITAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:227330" />
        <display value="FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:227400" />
        <display value="FACTOR V DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:227500" />
        <display value="FACTOR VII DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:227600" />
        <display value="FACTOR X DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:227645" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP C" />
      </concept>
      <concept>
        <code value="OMIM:227646" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP D2" />
      </concept>
      <concept>
        <code value="OMIM:227650" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP A" />
      </concept>
      <concept>
        <code value="OMIM:227810" />
        <display value="FANCONI-BICKEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:227850" />
        <display value="FANCONI-LIKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:228000" />
        <display value="FARBER LIPOGRANULOMATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:228020" />
        <display value="FASCIAL DYSTROPHY, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:228100" />
        <display value="VISCERAL STEATOSIS, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:228200" />
        <display value="FEMUR-FIBULA-ULNA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:228250" />
        <display value="FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:228300" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:228355" />
        <display value="FETAL IODINE DEFICIENCY DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:228400" />
        <display value="FEVER, FAMILIAL LIFELONG PERSISTENT" />
      </concept>
      <concept>
        <code value="OMIM:228520" />
        <display value="FIBROCHONDROGENESIS 1" />
      </concept>
      <concept>
        <code value="OMIM:228550" />
        <display value="MYOFIBROMATOSIS, INFANTILE, 1" />
      </concept>
      <concept>
        <code value="OMIM:228560" />
        <display value="FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES" />
      </concept>
      <concept>
        <code value="OMIM:228600" />
        <display value="HYALINE FIBROMATOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:228800" />
        <display value="FIBROSCLEROSIS, MULTIFOCAL" />
      </concept>
      <concept>
        <code value="OMIM:228900" />
        <display value="FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:228930" />
        <display value="FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:228940" />
        <display value="FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:228960" />
        <display value="HIGH MOLECULAR WEIGHT KININOGEN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:228980" />
        <display value="FLECK RETINA, FAMILIAL BENIGN" />
      </concept>
      <concept>
        <code value="OMIM:228990" />
        <display value="FLECK RETINA OF KANDORI" />
      </concept>
      <concept>
        <code value="OMIM:229045" />
        <display value="FOCAL EPITHELIAL HYPERPLASIA, ORAL" />
      </concept>
      <concept>
        <code value="OMIM:229050" />
        <display value="FOLATE MALABSORPTION, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:229070" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:229100" />
        <display value="GLUTAMATE FORMIMINOTRANSFERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:229120" />
        <display value="FOUNTAIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:229200" />
        <display value="BRITTLE CORNEA SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:229230" />
        <display value="FRASER-LIKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:229250" />
        <display value="FREESIA FLOWERS, INABILITY TO SMELL" />
      </concept>
      <concept>
        <code value="OMIM:229300" />
        <display value="FRIEDREICH ATAXIA 1" />
      </concept>
      <concept>
        <code value="OMIM:229310" />
        <display value="FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA" />
      </concept>
      <concept>
        <code value="OMIM:229400" />
        <display value="FRONTOFACIONASAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:229500" />
        <display value="FRUCTOSE AND GALACTOSE INTOLERANCE" />
      </concept>
      <concept>
        <code value="OMIM:229600" />
        <display value="FRUCTOSE INTOLERANCE, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:229650" />
        <display value="FRUCTOSE UTILIZATION" />
      </concept>
      <concept>
        <code value="OMIM:229700" />
        <display value="FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:229800" />
        <display value="FRUCTOSURIA, ESSENTIAL" />
      </concept>
      <concept>
        <code value="OMIM:229850" />
        <display value="FRYNS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:230000" />
        <display value="FUCOSIDOSIS" />
      </concept>
      <concept>
        <code value="OMIM:230200" />
        <display value="GALACTOKINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:230300" />
        <display value="GALACTORRHEA" />
      </concept>
      <concept>
        <code value="OMIM:230350" />
        <display value="GALACTOSE EPIMERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:230400" />
        <display value="GALACTOSEMIA" />
      </concept>
      <concept>
        <code value="OMIM:230450" />
        <display value="GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:230500" />
        <display value="GM1-GANGLIOSIDOSIS, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:230600" />
        <display value="GM1-GANGLIOSIDOSIS, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:230650" />
        <display value="GM1-GANGLIOSIDOSIS, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:230740" />
        <display value="GAPO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:230750" />
        <display value="GASTROSCHISIS" />
      </concept>
      <concept>
        <code value="OMIM:230800" />
        <display value="GAUCHER DISEASE, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:230900" />
        <display value="GAUCHER DISEASE, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:231000" />
        <display value="GAUCHER DISEASE, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:231005" />
        <display value="GAUCHER DISEASE, TYPE IIIC" />
      </concept>
      <concept>
        <code value="OMIM:231050" />
        <display value="GELEOPHYSIC DYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:231060" />
        <display value="GENITOPALATOCARDIAC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:231070" />
        <display value="GERODERMA OSTEODYSPLASTICUM" />
      </concept>
      <concept>
        <code value="OMIM:231080" />
        <display value="GERMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:231090" />
        <display value="HYDATIDIFORM MOLE, RECURRENT, 1" />
      </concept>
      <concept>
        <code value="OMIM:231095" />
        <display value="GHOSAL HEMATODIAPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:231100" />
        <display value="HEMOCHROMATOSIS, NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:231200" />
        <display value="BERNARD-SOULIER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:231300" />
        <display value="GLAUCOMA 3, PRIMARY CONGENITAL, A" />
      </concept>
      <concept>
        <code value="OMIM:231530" />
        <display value="3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:231550" />
        <display value="ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:231630" />
        <display value="MONOSODIUM GLUTAMATE SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:231670" />
        <display value="GLUTARIC ACIDEMIA I" />
      </concept>
      <concept>
        <code value="OMIM:231680" />
        <display value="MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:231690" />
        <display value="GLUTARIC ACIDURIA III" />
      </concept>
      <concept>
        <code value="OMIM:231900" />
        <display value="GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:231950" />
        <display value="GLUTATHIONURIA" />
      </concept>
      <concept>
        <code value="OMIM:231970" />
        <display value="GLUTEAL MUSCLES, ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:232200" />
        <display value="GLYCOGEN STORAGE DISEASE Ia" />
      </concept>
      <concept>
        <code value="OMIM:232220" />
        <display value="GLYCOGEN STORAGE DISEASE Ib" />
      </concept>
      <concept>
        <code value="OMIM:232240" />
        <display value="GLYCOGEN STORAGE DISEASE Ic" />
      </concept>
      <concept>
        <code value="OMIM:232300" />
        <display value="GLYCOGEN STORAGE DISEASE II" />
      </concept>
      <concept>
        <code value="OMIM:232400" />
        <display value="GLYCOGEN STORAGE DISEASE III" />
      </concept>
      <concept>
        <code value="OMIM:232500" />
        <display value="GLYCOGEN STORAGE DISEASE IV" />
      </concept>
      <concept>
        <code value="OMIM:232600" />
        <display value="GLYCOGEN STORAGE DISEASE V" />
      </concept>
      <concept>
        <code value="OMIM:232700" />
        <display value="GLYCOGEN STORAGE DISEASE VI" />
      </concept>
      <concept>
        <code value="OMIM:232800" />
        <display value="GLYCOGEN STORAGE DISEASE VII" />
      </concept>
      <concept>
        <code value="OMIM:232900" />
        <display value="GLYCOPROTEIN STORAGE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:233100" />
        <display value="RENAL GLUCOSURIA" />
      </concept>
      <concept>
        <code value="OMIM:233270" />
        <display value="GOMBO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:233300" />
        <display value="OVARIAN DYSGENESIS 1" />
      </concept>
      <concept>
        <code value="OMIM:233400" />
        <display value="PERRAULT SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:233420" />
        <display value="46,XY SEX REVERSAL 7" />
      </concept>
      <concept>
        <code value="OMIM:233430" />
        <display value="GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:233450" />
        <display value="GOODPASTURE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:233600" />
        <display value="GRANULOCYTOPENIA WITH IMMUNOGLOBULIN ABNORMALITY" />
      </concept>
      <concept>
        <code value="OMIM:233650" />
        <display value="COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS" />
      </concept>
      <concept>
        <code value="OMIM:233670" />
        <display value="GRANULOMATOUS DISEASE WITH DEFECT IN NEUTROPHIL CHEMOTAXIS" />
      </concept>
      <concept>
        <code value="OMIM:233690" />
        <display value="GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE" />
      </concept>
      <concept>
        <code value="OMIM:233700" />
        <display value="GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:233710" />
        <display value="GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:233800" />
        <display value="GROUPED PIGMENTATION OF THE RETINA" />
      </concept>
      <concept>
        <code value="OMIM:233805" />
        <display value="GROWTH FACTORS, COMBINED DEFECT OF" />
      </concept>
      <concept>
        <code value="OMIM:233810" />
        <display value="GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA" />
      </concept>
      <concept>
        <code value="OMIM:233910" />
        <display value="HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B" />
      </concept>
      <concept>
        <code value="OMIM:234000" />
        <display value="FACTOR XII DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:234030" />
        <display value="HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:234050" />
        <display value="TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:234100" />
        <display value="HALLERMANN-STREIFF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:234200" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1" />
      </concept>
      <concept>
        <code value="OMIM:234250" />
        <display value="HALL-RIGGS MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:234280" />
        <display value="HALLUX VARUS AND PREAXIAL POLYSYNDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:234300" />
        <display value="HALO NEVI" />
      </concept>
      <concept>
        <code value="OMIM:234350" />
        <display value="HALOTHANE HEPATITIS" />
      </concept>
      <concept>
        <code value="OMIM:234500" />
        <display value="HARTNUP DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:234580" />
        <display value="HEIMLER SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:234700" />
        <display value="HEART BLOCK, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:234750" />
        <display value="HEART, MALFORMATION OF" />
      </concept>
      <concept>
        <code value="OMIM:234800" />
        <display value="HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:234810" />
        <display value="PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:234820" />
        <display value="HEMANGIOPERICYTOMA, MALIGNANT" />
      </concept>
      <concept>
        <code value="OMIM:235000" />
        <display value="HEMIHYPERPLASIA, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:235200" />
        <display value="HEMOCHROMATOSIS, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:235255" />
        <display value="MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:235370" />
        <display value="HEMOLYTIC ANEMIA WITH THERMAL SENSITIVITY OF RED CELLS" />
      </concept>
      <concept>
        <code value="OMIM:235400" />
        <display value="HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:235500" />
        <display value="HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN" />
      </concept>
      <concept>
        <code value="OMIM:235510" />
        <display value="HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:235550" />
        <display value="HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:235555" />
        <display value="BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:235700" />
        <display value="HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:235730" />
        <display value="MOWAT-WILSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:235740" />
        <display value="HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:235750" />
        <display value="HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIG TOES, AND VENTRICULAR SEPTAL DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:235760" />
        <display value="HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIAL FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:235800" />
        <display value="HISTIDINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:235830" />
        <display value="HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:235900" />
        <display value="HISTIOCYTOSIS, FAMILIAL LIPOCHROME" />
      </concept>
      <concept>
        <code value="OMIM:236000" />
        <display value="LYMPHOMA, HODGKIN, CLASSIC" />
      </concept>
      <concept>
        <code value="OMIM:236100" />
        <display value="HOLOPROSENCEPHALY 1" />
      </concept>
      <concept>
        <code value="OMIM:236110" />
        <display value="HOLZGREVE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:236130" />
        <display value="HOMOCARNOSINOSIS" />
      </concept>
      <concept>
        <code value="OMIM:236200" />
        <display value="HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:236250" />
        <display value="HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY" />
      </concept>
      <concept>
        <code value="OMIM:236270" />
        <display value="HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE" />
      </concept>
      <concept>
        <code value="OMIM:236300" />
        <display value="HOOFT DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:236400" />
        <display value="HUMERORADIAL SYNOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:236410" />
        <display value="HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:236450" />
        <display value="HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:236500" />
        <display value="MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:236600" />
        <display value="HYDROCEPHALUS, CONGENITAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:236635" />
        <display value="HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS" />
      </concept>
      <concept>
        <code value="OMIM:236640" />
        <display value="HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:236660" />
        <display value="HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS" />
      </concept>
      <concept>
        <code value="OMIM:236670" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1" />
      </concept>
      <concept>
        <code value="OMIM:236680" />
        <display value="HYDROLETHALUS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:236690" />
        <display value="HYDROCEPHALUS, NORMAL-PRESSURE" />
      </concept>
      <concept>
        <code value="OMIM:236700" />
        <display value="MCKUSICK-KAUFMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:236730" />
        <display value="UROFACIAL SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:236750" />
        <display value="HYDROPS FETALIS, NONIMMUNE" />
      </concept>
      <concept>
        <code value="OMIM:236792" />
        <display value="L-2-HYDROXYGLUTARIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:236795" />
        <display value="3-HYDROXYISOBUTYRIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:236800" />
        <display value="HYDROXYKYNURENINURIA" />
      </concept>
      <concept>
        <code value="OMIM:236900" />
        <display value="HYDROXYLYSINURIA" />
      </concept>
      <concept>
        <code value="OMIM:237000" />
        <display value="HYDROXYPROLINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:237100" />
        <display value="HYMEN, IMPERFORATE" />
      </concept>
      <concept>
        <code value="OMIM:237300" />
        <display value="CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:237310" />
        <display value="N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:237400" />
        <display value="HYPER-BETA-ALANINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:237450" />
        <display value="HYPERBILIRUBINEMIA, ROTOR TYPE" />
      </concept>
      <concept>
        <code value="OMIM:237500" />
        <display value="DUBIN-JOHNSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:237550" />
        <display value="HYPERBILIRUBINEMIA, CONJUGATED, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:237800" />
        <display value="HYPERBILIRUBINEMIA, SHUNT, PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:237900" />
        <display value="HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:238320" />
        <display value="LEYDIG CELL HYPOPLASIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:238340" />
        <display value="HYPERLEUCINE-ISOLEUCINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:238350" />
        <display value="HYPERLEXIA" />
      </concept>
      <concept>
        <code value="OMIM:238600" />
        <display value="HYPERLIPOPROTEINEMIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:238700" />
        <display value="HYPERLYSINEMIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:238710" />
        <display value="HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA" />
      </concept>
      <concept>
        <code value="OMIM:238750" />
        <display value="HYPERLYSINURIA WITH HYPERAMMONEMIA" />
      </concept>
      <concept>
        <code value="OMIM:238800" />
        <display value="HYPERMETABOLISM DUE TO DEFECT IN MITOCHONDRIA" />
      </concept>
      <concept>
        <code value="OMIM:238950" />
        <display value="HYPEROPIA, HIGH" />
      </concept>
      <concept>
        <code value="OMIM:238970" />
        <display value="HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:239000" />
        <display value="PAGET DISEASE OF BONE 5, JUVENILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:239100" />
        <display value="VAN BUCHEM DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:239199" />
        <display value="HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA" />
      </concept>
      <concept>
        <code value="OMIM:239200" />
        <display value="HYPERPARATHYROIDISM, NEONATAL SEVERE" />
      </concept>
      <concept>
        <code value="OMIM:239300" />
        <display value="HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:239350" />
        <display value="HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:239500" />
        <display value="HYPERPROLINEMIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:239510" />
        <display value="HYPERPROLINEMIA, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:239710" />
        <display value="ACROFRONTOFACIONASAL DYSOSTOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:239711" />
        <display value="HYPERTELORISM AND TETRALOGY OF FALLOT" />
      </concept>
      <concept>
        <code value="OMIM:239800" />
        <display value="HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:239840" />
        <display value="HYPERTRICHOSIS, CONGENITAL ANTERIOR CERVICAL, WITH PERIPHERAL SENSORY AND MOTOR NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:239850" />
        <display value="CANTU SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:239900" />
        <display value="HYPERTROPHIC NEUROPATHY AND CATARACT" />
      </concept>
      <concept>
        <code value="OMIM:240000" />
        <display value="HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE" />
      </concept>
      <concept>
        <code value="OMIM:240150" />
        <display value="HYPERVITAMINOSIS A, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:240200" />
        <display value="HYPOADRENOCORTICISM, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:240300" />
        <display value="AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I, WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:240400" />
        <display value="HYPOASCORBEMIA" />
      </concept>
      <concept>
        <code value="OMIM:240500" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 2" />
      </concept>
      <concept>
        <code value="OMIM:240600" />
        <display value="GLYCOGEN STORAGE DISEASE 0, LIVER" />
      </concept>
      <concept>
        <code value="OMIM:240800" />
        <display value="HYPOGLYCEMIA, LEUCINE-INDUCED" />
      </concept>
      <concept>
        <code value="OMIM:240900" />
        <display value="HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:240950" />
        <display value="HYPOGONADISM-CATARACT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:241000" />
        <display value="HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:241080" />
        <display value="WOODHOUSE-SAKATI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:241090" />
        <display value="HYPERGONADOTROPIC HYPOGONADISM AND PARTIAL ALOPECIA" />
      </concept>
      <concept>
        <code value="OMIM:241100" />
        <display value="HYPOGONADISM, MALE" />
      </concept>
      <concept>
        <code value="OMIM:241120" />
        <display value="HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES" />
      </concept>
      <concept>
        <code value="OMIM:241150" />
        <display value="HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:241200" />
        <display value="BARTTER SYNDROME, TYPE 2, ANTENATAL" />
      </concept>
      <concept>
        <code value="OMIM:241310" />
        <display value="HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:241410" />
        <display value="HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:241500" />
        <display value="HYPOPHOSPHATASIA, INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:241510" />
        <display value="HYPOPHOSPHATASIA, CHILDHOOD" />
      </concept>
      <concept>
        <code value="OMIM:241519" />
        <display value="HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS" />
      </concept>
      <concept>
        <code value="OMIM:241520" />
        <display value="HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:241530" />
        <display value="HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:241540" />
        <display value="HYPOPITUITARISM, CONGENITAL, WITH CENTRAL DIABETES INSIPIDUS" />
      </concept>
      <concept>
        <code value="OMIM:241550" />
        <display value="HYPOPLASTIC LEFT HEART SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:241600" />
        <display value="IMMUNODEFICIENCY 43" />
      </concept>
      <concept>
        <code value="OMIM:241760" />
        <display value="HYPOSPADIAS-MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:241800" />
        <display value="HYPOTHALAMIC HAMARTOMAS" />
      </concept>
      <concept>
        <code value="OMIM:241850" />
        <display value="HYPOTHYROIDISM, THYROIDAL OR ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE" />
      </concept>
      <concept>
        <code value="OMIM:242050" />
        <display value="HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY" />
      </concept>
      <concept>
        <code value="OMIM:242100" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:242150" />
        <display value="ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:242300" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1" />
      </concept>
      <concept>
        <code value="OMIM:242400" />
        <display value="ICHTHYOSIS CONGENITA WITH BILIARY ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:242500" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B" />
      </concept>
      <concept>
        <code value="OMIM:242510" />
        <display value="ICHTHYOSIS WITH ALOPECIA, ECLABIUM, ECTROPION, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:242520" />
        <display value="ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:242530" />
        <display value="ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT" />
      </concept>
      <concept>
        <code value="OMIM:242550" />
        <display value="ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:242600" />
        <display value="IMINOGLYCINURIA" />
      </concept>
      <concept>
        <code value="OMIM:242670" />
        <display value="CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES" />
      </concept>
      <concept>
        <code value="OMIM:242680" />
        <display value="CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA" />
      </concept>
      <concept>
        <code value="OMIM:242700" />
        <display value="IMMUNE DEFECT DUE TO ABSENCE OF THYMUS" />
      </concept>
      <concept>
        <code value="OMIM:242840" />
        <display value="VICI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:242850" />
        <display value="IMMUNE DEFICIENCY DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:242860" />
        <display value="IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:242870" />
        <display value="IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTS AND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES" />
      </concept>
      <concept>
        <code value="OMIM:242880" />
        <display value="IMMUNOERYTHROMYELOID HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:242890" />
        <display value="IMMUNOGLOBULIN D LEVEL IN PLASMA, LOW" />
      </concept>
      <concept>
        <code value="OMIM:242900" />
        <display value="SCHIMKE IMMUNOOSSEOUS DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:243000" />
        <display value="INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:243050" />
        <display value="INDOLYLACROYL GLYCINURIA WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:243060" />
        <display value="SPERMATOGENIC FAILURE 5" />
      </concept>
      <concept>
        <code value="OMIM:243080" />
        <display value="INOSINE PHOSPHORYLASE DEFICIENCY, IMMUNE DEFECT DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:243100" />
        <display value="INTERNAL CAROTID ARTERIES, HYPOPLASIA OF" />
      </concept>
      <concept>
        <code value="OMIM:243110" />
        <display value="IMMUNODEFICIENCY WITH DEFECTIVE T-CELL RESPONSE TO INTERLEUKIN 1" />
      </concept>
      <concept>
        <code value="OMIM:243150" />
        <display value="GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:243180" />
        <display value="VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:243185" />
        <display value="INTESTINAL PSEUDOOBSTRUCTION WITH PATENT DUCTUS ARTERIOSUS AND NATAL TEETH" />
      </concept>
      <concept>
        <code value="OMIM:243200" />
        <display value="INTRACRANIAL HYPERTENSION, IDIOPATHIC" />
      </concept>
      <concept>
        <code value="OMIM:243300" />
        <display value="CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:243310" />
        <display value="BARAITSER-WINTER SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:243320" />
        <display value="INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:243400" />
        <display value="ACETYLATION, SLOW" />
      </concept>
      <concept>
        <code value="OMIM:243440" />
        <display value="ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:243450" />
        <display value="ISOVALERIC ACID, INABILITY TO SMELL" />
      </concept>
      <concept>
        <code value="OMIM:243500" />
        <display value="ISOVALERIC ACIDEMIA" />
      </concept>
      <concept>
        <code value="OMIM:243600" />
        <display value="JEJUNAL ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:243605" />
        <display value="STROMME SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:243700" />
        <display value="HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:243800" />
        <display value="JOHANSON-BLIZZARD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:243910" />
        <display value="ARIMA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:244100" />
        <display value="JUMPING FRENCHMEN OF MAINE" />
      </concept>
      <concept>
        <code value="OMIM:244200" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:244300" />
        <display value="KAPUR-TORIELLO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:244400" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:244450" />
        <display value="KAUFMAN OCULOCEREBROFACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:244460" />
        <display value="KENNY-CAFFEY SYNDROME, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:244510" />
        <display value="KERATOCONUS AND CONGENITAL HIP DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:244600" />
        <display value="KERATOCONUS POSTICUS CIRCUMSCRIPTUS" />
      </concept>
      <concept>
        <code value="OMIM:244850" />
        <display value="PALMOPLANTAR KERATODERMA, NORRBOTTEN RECESSIVE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:245000" />
        <display value="PAPILLON-LEFEVRE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:245010" />
        <display value="HAIM-MUNK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:245050" />
        <display value="SUCCINYL-CoA:3-OXOACID-CoA TRANSFERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:245100" />
        <display value="RICHARDS-RUNDLE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:245130" />
        <display value="KETOADIPICACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:245150" />
        <display value="KEUTEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:245160" />
        <display value="KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS" />
      </concept>
      <concept>
        <code value="OMIM:245180" />
        <display value="KIFAFA SEIZURE DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:245190" />
        <display value="KNIEST-LIKE DYSPLASIA, LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:245200" />
        <display value="KRABBE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:245300" />
        <display value="KURU, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:245340" />
        <display value="ERYTHROCYTE LACTATE TRANSPORTER DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:245348" />
        <display value="PYRUVATE DEHYDROGENASE E2 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:245349" />
        <display value="PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:245400" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA)" />
      </concept>
      <concept>
        <code value="OMIM:245450" />
        <display value="LACTIC ACIDURIA DUE TO D-LACTIC ACID" />
      </concept>
      <concept>
        <code value="OMIM:245480" />
        <display value="SPECIFIC GRANULE DEFICIENCY 1" />
      </concept>
      <concept>
        <code value="OMIM:245550" />
        <display value="LAMBERT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:245552" />
        <display value="LAMBOTTE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:245570" />
        <display value="EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:245590" />
        <display value="GROWTH HORMONE INSENSITIVITY WITH IMMUNODEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:245600" />
        <display value="MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:245650" />
        <display value="LARSEN-LIKE SYNDROME, LETHAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:245660" />
        <display value="LARYNGOONYCHOCUTANEOUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:245800" />
        <display value="LAURENCE-MOON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:245900" />
        <display value="LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:246000" />
        <display value="LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT" />
      </concept>
      <concept>
        <code value="OMIM:246200" />
        <display value="DONOHUE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:246300" />
        <display value="LEPROSY, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:246400" />
        <display value="LETTERER-SIWE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:246450" />
        <display value="3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:246470" />
        <display value="LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER" />
      </concept>
      <concept>
        <code value="OMIM:246500" />
        <display value="LEUKOMELANODERMA, INFANTILISM, MENTAL RETARDATION, HYPODONTIA, HYPOTRICHOSIS" />
      </concept>
      <concept>
        <code value="OMIM:246550" />
        <display value="LICHTENSTEIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:246555" />
        <display value="LIMB DEFECTS, DISTAL TRANSVERSE, WITH MENTAL RETARDATION AND SPASTICITY" />
      </concept>
      <concept>
        <code value="OMIM:246560" />
        <display value="SPLIT-HAND/FOOT MALFORMATION 3" />
      </concept>
      <concept>
        <code value="OMIM:246570" />
        <display value="FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:246650" />
        <display value="LIPASE DEFICIENCY, COMBINED" />
      </concept>
      <concept>
        <code value="OMIM:246700" />
        <display value="CHYLOMICRON RETENTION DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:246900" />
        <display value="DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:247100" />
        <display value="LIPOID PROTEINOSIS OF URBACH AND WIETHE" />
      </concept>
      <concept>
        <code value="OMIM:247150" />
        <display value="LIP PRINTS" />
      </concept>
      <concept>
        <code value="OMIM:247200" />
        <display value="MILLER-DIEKER LISSENCEPHALY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:247410" />
        <display value="LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:247420" />
        <display value="LUTHERAN NULL" />
      </concept>
      <concept>
        <code value="OMIM:247430" />
        <display value="LYMPHOBLASTIC TRANSFORMATION, INHIBITION OF" />
      </concept>
      <concept>
        <code value="OMIM:247440" />
        <display value="LYMPHEDEMA, CONGENITAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:247450" />
        <display value="LYMPHOBLASTIC TRANSFORMATION, INTRINSIC DEFECT IN" />
      </concept>
      <concept>
        <code value="OMIM:247610" />
        <display value="LYMPHOID INTERSTITIAL PNEUMONIA" />
      </concept>
      <concept>
        <code value="OMIM:247630" />
        <display value="LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:247640" />
        <display value="LYMPHOBLASTIC LEUKEMIA, ACUTE, WITH LYMPHOMATOUS FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:247650" />
        <display value="LYMPHOKINE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:247800" />
        <display value="LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNE HEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS" />
      </concept>
      <concept>
        <code value="OMIM:247950" />
        <display value="LYSINE MALABSORPTION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:247990" />
        <display value="MACDERMOT-WINTER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:248000" />
        <display value="MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:248010" />
        <display value="MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE" />
      </concept>
      <concept>
        <code value="OMIM:248100" />
        <display value="MACROSOMIA ADIPOSA CONGENITA" />
      </concept>
      <concept>
        <code value="OMIM:248110" />
        <display value="MACROSOMIA WITH MICROPHTHALMIA, LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:248190" />
        <display value="HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT" />
      </concept>
      <concept>
        <code value="OMIM:248200" />
        <display value="STARGARDT DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:248250" />
        <display value="HYPOMAGNESEMIA 3, RENAL" />
      </concept>
      <concept>
        <code value="OMIM:248260" />
        <display value="MAGNESIUM, ELEVATED RED CELL" />
      </concept>
      <concept>
        <code value="OMIM:248300" />
        <display value="MAL DE MELEDA" />
      </concept>
      <concept>
        <code value="OMIM:248310" />
        <display value="PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL" />
      </concept>
      <concept>
        <code value="OMIM:248340" />
        <display value="3MC SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:248350" />
        <display value="MALOCCLUSION AND SHORT STATURE" />
      </concept>
      <concept>
        <code value="OMIM:248360" />
        <display value="MALONYL-CoA DECARBOXYLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:248370" />
        <display value="MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:248390" />
        <display value="TREACHER COLLINS SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:248400" />
        <display value="MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:248450" />
        <display value="MANITOBA OCULOTRICHOANAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:248500" />
        <display value="MANNOSIDOSIS, ALPHA B, LYSOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:248510" />
        <display value="MANNOSIDOSIS, BETA A, LYSOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:248600" />
        <display value="MAPLE SYRUP URINE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:248700" />
        <display value="MARDEN-WALKER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:248760" />
        <display value="MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS" />
      </concept>
      <concept>
        <code value="OMIM:248770" />
        <display value="MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:248800" />
        <display value="MARINESCO-SJOGREN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:248900" />
        <display value="MAST SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:248910" />
        <display value="CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA" />
      </concept>
      <concept>
        <code value="OMIM:248950" />
        <display value="MCDONOUGH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:249000" />
        <display value="MECKEL SYNDROME, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:249100" />
        <display value="FAMILIAL MEDITERRANEAN FEVER" />
      </concept>
      <concept>
        <code value="OMIM:249230" />
        <display value="MEGAEPIPHYSEAL DWARFISM" />
      </concept>
      <concept>
        <code value="OMIM:249240" />
        <display value="MEGALENCEPHALY WITH DYSMYELINATION" />
      </concept>
      <concept>
        <code value="OMIM:249270" />
        <display value="THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:249300" />
        <display value="MEGALOCORNEA" />
      </concept>
      <concept>
        <code value="OMIM:249310" />
        <display value="MEGALOCORNEA-MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:249400" />
        <display value="MELANOSIS, NEUROCUTANEOUS" />
      </concept>
      <concept>
        <code value="OMIM:249420" />
        <display value="FRANK-TER HAAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:249500" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1" />
      </concept>
      <concept>
        <code value="OMIM:249599" />
        <display value="MENTAL RETARDATION SYNDROME, BELGIAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:249600" />
        <display value="MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:249620" />
        <display value="OHDO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:249630" />
        <display value="MENTAL RETARDATION, BUENOS AIRES TYPE" />
      </concept>
      <concept>
        <code value="OMIM:249650" />
        <display value="MERCAPTOLACTATE-CYSTEINE DISULFIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:249660" />
        <display value="MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:249670" />
        <display value="MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION" />
      </concept>
      <concept>
        <code value="OMIM:249700" />
        <display value="LANGER MESOMELIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:249710" />
        <display value="MESOMELIC LIMB SHORTENING AND BOWING" />
      </concept>
      <concept>
        <code value="OMIM:249900" />
        <display value="METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:250100" />
        <display value="METACHROMATIC LEUKODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:250215" />
        <display value="METAPHYSEAL ACROSCYPHODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:250220" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:250230" />
        <display value="METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:250250" />
        <display value="CARTILAGE-HAIR HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:250300" />
        <display value="METAPHYSEAL CHONDRODYSPLASIA, PENA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:250400" />
        <display value="METAPHYSEAL DYSPLASIA, SPAHR TYPE" />
      </concept>
      <concept>
        <code value="OMIM:250410" />
        <display value="RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:250420" />
        <display value="METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:250450" />
        <display value="METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:250460" />
        <display value="METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS" />
      </concept>
      <concept>
        <code value="OMIM:250500" />
        <display value="METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA" />
      </concept>
      <concept>
        <code value="OMIM:250620" />
        <display value="3-HYDROXYISOBUTYRYL-CoA HYDROLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:250650" />
        <display value="METHANE PRODUCTION" />
      </concept>
      <concept>
        <code value="OMIM:250700" />
        <display value="METHEMOGLOBIN REDUCTASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:250790" />
        <display value="METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA" />
      </concept>
      <concept>
        <code value="OMIM:250800" />
        <display value="METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE" />
      </concept>
      <concept>
        <code value="OMIM:250850" />
        <display value="METHIONINE ADENOSYLTRANSFERASE I/III DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:250900" />
        <display value="METHIONINE MALABSORPTION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:250940" />
        <display value="HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblG COMPLEMENTATION TYPE" />
      </concept>
      <concept>
        <code value="OMIM:250950" />
        <display value="3-METHYLGLUTACONIC ACIDURIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:250951" />
        <display value="3-METHYLGLUTACONIC ACIDURIA, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:251000" />
        <display value="METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:251100" />
        <display value="METHYLMALONIC ACIDURIA, cblA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:251110" />
        <display value="METHYLMALONIC ACIDURIA, cblB TYPE" />
      </concept>
      <concept>
        <code value="OMIM:251120" />
        <display value="METHYLMALONYL-CoA EPIMERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:251190" />
        <display value="MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE" />
      </concept>
      <concept>
        <code value="OMIM:251200" />
        <display value="MICROCEPHALY 1, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:251220" />
        <display value="MICROCEPHALY-CARDIOMYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:251230" />
        <display value="MICROCEPHALY-MICROMELIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:251240" />
        <display value="MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:251250" />
        <display value="MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:251255" />
        <display value="JAWAD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:251260" />
        <display value="NIJMEGEN BREAKAGE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:251270" />
        <display value="MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:251280" />
        <display value="MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS" />
      </concept>
      <concept>
        <code value="OMIM:251290" />
        <display value="PSEUDO-TORCH SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:251300" />
        <display value="GALLOWAY-MOWAT SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:251400" />
        <display value="MICROCOLON" />
      </concept>
      <concept>
        <code value="OMIM:251450" />
        <display value="DESBUQUOIS DYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:251505" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 4" />
      </concept>
      <concept>
        <code value="OMIM:251600" />
        <display value="MICROPHTHALMIA, ISOLATED 1" />
      </concept>
      <concept>
        <code value="OMIM:251700" />
        <display value="MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA, AND DENTAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:251750" />
        <display value="MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA" />
      </concept>
      <concept>
        <code value="OMIM:251800" />
        <display value="MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:251850" />
        <display value="DIARRHEA 2, WITH MICROVILLUS ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:251880" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:251900" />
        <display value="MITOCHONDRIAL MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:251945" />
        <display value="MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT" />
      </concept>
      <concept>
        <code value="OMIM:251950" />
        <display value="MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS" />
      </concept>
      <concept>
        <code value="OMIM:252010" />
        <display value="MITOCHONDRIAL COMPLEX I DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:252011" />
        <display value="MITOCHONDRIAL COMPLEX II DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:252100" />
        <display value="MOHR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:252150" />
        <display value="MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A" />
      </concept>
      <concept>
        <code value="OMIM:252160" />
        <display value="MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B" />
      </concept>
      <concept>
        <code value="OMIM:252250" />
        <display value="MONOCYTE CHEMOTACTIC DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:252270" />
        <display value="MONOSOMY 7 OF BONE MARROW" />
      </concept>
      <concept>
        <code value="OMIM:252300" />
        <display value="MORQUIO SYNDROME C" />
      </concept>
      <concept>
        <code value="OMIM:252320" />
        <display value="MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA" />
      </concept>
      <concept>
        <code value="OMIM:252350" />
        <display value="MOYAMOYA DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:252500" />
        <display value="MUCOLIPIDOSIS II ALPHA/BETA" />
      </concept>
      <concept>
        <code value="OMIM:252600" />
        <display value="MUCOLIPIDOSIS III ALPHA/BETA" />
      </concept>
      <concept>
        <code value="OMIM:252605" />
        <display value="MUCOLIPIDOSIS III GAMMA" />
      </concept>
      <concept>
        <code value="OMIM:252650" />
        <display value="MUCOLIPIDOSIS IV" />
      </concept>
      <concept>
        <code value="OMIM:252700" />
        <display value="MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES" />
      </concept>
      <concept>
        <code value="OMIM:252900" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE IIIA" />
      </concept>
      <concept>
        <code value="OMIM:252920" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE IIIB" />
      </concept>
      <concept>
        <code value="OMIM:252930" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE IIIC" />
      </concept>
      <concept>
        <code value="OMIM:252940" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE IIID" />
      </concept>
      <concept>
        <code value="OMIM:253000" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE IVA" />
      </concept>
      <concept>
        <code value="OMIM:253010" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE IVB" />
      </concept>
      <concept>
        <code value="OMIM:253200" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE VI" />
      </concept>
      <concept>
        <code value="OMIM:253220" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE VII" />
      </concept>
      <concept>
        <code value="OMIM:253240" />
        <display value="MUCUS INSPISSATION OF RESPIRATORY TRACT" />
      </concept>
      <concept>
        <code value="OMIM:253250" />
        <display value="MULIBREY NANISM" />
      </concept>
      <concept>
        <code value="OMIM:253260" />
        <display value="BIOTINIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:253270" />
        <display value="HOLOCARBOXYLASE SYNTHETASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:253280" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3" />
      </concept>
      <concept>
        <code value="OMIM:253290" />
        <display value="MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:253300" />
        <display value="SPINAL MUSCULAR ATROPHY, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:253310" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:253320" />
        <display value="MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPIC HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:253400" />
        <display value="SPINAL MUSCULAR ATROPHY, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:253550" />
        <display value="SPINAL MUSCULAR ATROPHY, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:253590" />
        <display value="MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:253600" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 1" />
      </concept>
      <concept>
        <code value="OMIM:253601" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:253700" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 5" />
      </concept>
      <concept>
        <code value="OMIM:253800" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4" />
      </concept>
      <concept>
        <code value="OMIM:253900" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, PRODUCING ARTHROGRYPOSIS" />
      </concept>
      <concept>
        <code value="OMIM:254000" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, WITH INFANTILE CATARACT AND HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:254090" />
        <display value="ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1" />
      </concept>
      <concept>
        <code value="OMIM:254100" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION" />
      </concept>
      <concept>
        <code value="OMIM:254110" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 8" />
      </concept>
      <concept>
        <code value="OMIM:254120" />
        <display value="MUSCULAR HYPERTONIA, LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:254130" />
        <display value="MIYOSHI MUSCULAR DYSTROPHY 1" />
      </concept>
      <concept>
        <code value="OMIM:254150" />
        <display value="MUSK, INABILITY TO SMELL" />
      </concept>
      <concept>
        <code value="OMIM:254190" />
        <display value="MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS" />
      </concept>
      <concept>
        <code value="OMIM:254200" />
        <display value="MYASTHENIA GRAVIS" />
      </concept>
      <concept>
        <code value="OMIM:254210" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC" />
      </concept>
      <concept>
        <code value="OMIM:254300" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 10" />
      </concept>
      <concept>
        <code value="OMIM:254400" />
        <display value="MYCOSIS FUNGOIDES" />
      </concept>
      <concept>
        <code value="OMIM:254450" />
        <display value="MYELOFIBROSIS" />
      </concept>
      <concept>
        <code value="OMIM:254500" />
        <display value="MYELOMA, MULTIPLE" />
      </concept>
      <concept>
        <code value="OMIM:254600" />
        <display value="MYELOPEROXIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:254700" />
        <display value="MYELOPROLIFERATIVE DISEASE, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:254770" />
        <display value="EPILEPSY, MYOCLONIC JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:254780" />
        <display value="MYOCLONIC EPILEPSY OF LAFORA" />
      </concept>
      <concept>
        <code value="OMIM:254800" />
        <display value="MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG" />
      </concept>
      <concept>
        <code value="OMIM:254900" />
        <display value="EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE" />
      </concept>
      <concept>
        <code value="OMIM:254940" />
        <display value="CAREY-FINEMAN-ZITER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:254950" />
        <display value="MYOPATHY, GRANULOVACUOLAR LOBULAR, WITH ELECTRICAL MYOTONIA" />
      </concept>
      <concept>
        <code value="OMIM:254960" />
        <display value="MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:255100" />
        <display value="LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:255110" />
        <display value="CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED" />
      </concept>
      <concept>
        <code value="OMIM:255120" />
        <display value="CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:255125" />
        <display value="MYOPATHY WITH LACTIC ACIDOSIS, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:255140" />
        <display value="MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA" />
      </concept>
      <concept>
        <code value="OMIM:255160" />
        <display value="MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:255200" />
        <display value="MYOPATHY, CENTRONUCLEAR, 2" />
      </concept>
      <concept>
        <code value="OMIM:255300" />
        <display value="MYOPATHY, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:255310" />
        <display value="MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION" />
      </concept>
      <concept>
        <code value="OMIM:255320" />
        <display value="MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA" />
      </concept>
      <concept>
        <code value="OMIM:255500" />
        <display value="MYOPIA 18, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:255600" />
        <display value="MYOSCLEROSIS, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:255700" />
        <display value="MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:255710" />
        <display value="MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:255800" />
        <display value="SCHWARTZ-JAMPEL SYNDROME, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:255900" />
        <display value="MYXEDEMA" />
      </concept>
      <concept>
        <code value="OMIM:255960" />
        <display value="MYXOMA, INTRACARDIAC" />
      </concept>
      <concept>
        <code value="OMIM:255980" />
        <display value="NASODIGITOACOUSTIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:255990" />
        <display value="NATHALIE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:255995" />
        <display value="MYOPATHY, CONGENITAL, BAILEY-BLOCH" />
      </concept>
      <concept>
        <code value="OMIM:256000" />
        <display value="LEIGH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:256020" />
        <display value="NAIL-PATELLA-LIKE RENAL DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:256030" />
        <display value="NEMALINE MYOPATHY 2" />
      </concept>
      <concept>
        <code value="OMIM:256040" />
        <display value="PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:256050" />
        <display value="ATELOSTEOGENESIS, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:256100" />
        <display value="NEPHRONOPHTHISIS 1" />
      </concept>
      <concept>
        <code value="OMIM:256120" />
        <display value="NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM" />
      </concept>
      <concept>
        <code value="OMIM:256150" />
        <display value="NEPHROSIALIDOSIS" />
      </concept>
      <concept>
        <code value="OMIM:256200" />
        <display value="NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:256300" />
        <display value="NEPHROTIC SYNDROME, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:256370" />
        <display value="NEPHROTIC SYNDROME, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:256450" />
        <display value="HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:256500" />
        <display value="NETHERTON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:256520" />
        <display value="NEU-LAXOVA SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:256540" />
        <display value="GALACTOSIALIDOSIS" />
      </concept>
      <concept>
        <code value="OMIM:256550" />
        <display value="NEURAMINIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:256600" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A" />
      </concept>
      <concept>
        <code value="OMIM:256690" />
        <display value="NEUROFACIODIGITORENAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:256700" />
        <display value="NEUROBLASTOMA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:256710" />
        <display value="ELEJALDE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:256720" />
        <display value="NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY" />
      </concept>
      <concept>
        <code value="OMIM:256730" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:256731" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:256800" />
        <display value="INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS" />
      </concept>
      <concept>
        <code value="OMIM:256810" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:256840" />
        <display value="NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:256850" />
        <display value="GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:256855" />
        <display value="NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:256860" />
        <display value="NEUROPATHY, HEREDITARY SENSORY, ATYPICAL" />
      </concept>
      <concept>
        <code value="OMIM:256870" />
        <display value="NEUROPATHY, PAINFUL" />
      </concept>
      <concept>
        <code value="OMIM:257000" />
        <display value="NEUROVISCERAL STORAGE DISEASE WITH CURVILINEAR BODIES" />
      </concept>
      <concept>
        <code value="OMIM:257100" />
        <display value="NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA" />
      </concept>
      <concept>
        <code value="OMIM:257150" />
        <display value="NEUTROPHIL ACTIN DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:257200" />
        <display value="NIEMANN-PICK DISEASE, TYPE A" />
      </concept>
      <concept>
        <code value="OMIM:257220" />
        <display value="NIEMANN-PICK DISEASE, TYPE C1" />
      </concept>
      <concept>
        <code value="OMIM:257270" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B" />
      </concept>
      <concept>
        <code value="OMIM:257300" />
        <display value="MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:257320" />
        <display value="LISSENCEPHALY 2" />
      </concept>
      <concept>
        <code value="OMIM:257350" />
        <display value="NUCHAL BLEB, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:257400" />
        <display value="NYSTAGMUS, CONGENITAL, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:257500" />
        <display value="OBESITY-HYPOVENTILATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:257550" />
        <display value="OCULAR MOTOR APRAXIA" />
      </concept>
      <concept>
        <code value="OMIM:257600" />
        <display value="OCULAR MYOPATHY WITH CURARE SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:257790" />
        <display value="OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS" />
      </concept>
      <concept>
        <code value="OMIM:257800" />
        <display value="OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION" />
      </concept>
      <concept>
        <code value="OMIM:257850" />
        <display value="OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:257910" />
        <display value="OCULOPALATOCEREBRAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:257920" />
        <display value="3MC SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:257960" />
        <display value="OCULOTRICHODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:257970" />
        <display value="OCULORENOCEREBELLAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:257980" />
        <display value="ODONTOONYCHODERMAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:258040" />
        <display value="OEIS COMPLEX" />
      </concept>
      <concept>
        <code value="OMIM:258100" />
        <display value="OGUCHI DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:258150" />
        <display value="SPERMATOGENIC FAILURE 1" />
      </concept>
      <concept>
        <code value="OMIM:258200" />
        <display value="OLIVER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:258300" />
        <display value="OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:258315" />
        <display value="OMODYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:258320" />
        <display value="OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:258360" />
        <display value="ONYCHOTRICHODYSPLASIA AND NEUTROPENIA" />
      </concept>
      <concept>
        <code value="OMIM:258400" />
        <display value="OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS" />
      </concept>
      <concept>
        <code value="OMIM:258450" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1" />
      </concept>
      <concept>
        <code value="OMIM:258470" />
        <display value="OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA" />
      </concept>
      <concept>
        <code value="OMIM:258480" />
        <display value="OPSISMODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:258500" />
        <display value="OPTIC ATROPHY 6" />
      </concept>
      <concept>
        <code value="OMIM:258501" />
        <display value="3-METHYLGLUTACONIC ACIDURIA, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:258650" />
        <display value="OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:258660" />
        <display value="NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:258700" />
        <display value="OPTICOCOCHLEODENTATE DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:258800" />
        <display value="ORAL SENSIBILITY, DISTURBANCE OF" />
      </concept>
      <concept>
        <code value="OMIM:258840" />
        <display value="ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS" />
      </concept>
      <concept>
        <code value="OMIM:258850" />
        <display value="OROFACIODIGITAL SYNDROME III" />
      </concept>
      <concept>
        <code value="OMIM:258860" />
        <display value="OROFACIODIGITAL SYNDROME IV" />
      </concept>
      <concept>
        <code value="OMIM:258865" />
        <display value="OROFACIODIGITAL SYNDROME IX" />
      </concept>
      <concept>
        <code value="OMIM:258870" />
        <display value="GYRATE ATROPHY OF CHOROID AND RETINA" />
      </concept>
      <concept>
        <code value="OMIM:258900" />
        <display value="OROTIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:259050" />
        <display value="PRIMROSE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:259100" />
        <display value="HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:259200" />
        <display value="BLOUNT DISEASE, ADOLESCENT" />
      </concept>
      <concept>
        <code value="OMIM:259250" />
        <display value="OSTEODYSPLASIA, FAMILIAL, ANDERSON TYPE" />
      </concept>
      <concept>
        <code value="OMIM:259270" />
        <display value="OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI" />
      </concept>
      <concept>
        <code value="OMIM:259410" />
        <display value="OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS" />
      </concept>
      <concept>
        <code value="OMIM:259420" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:259440" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE IX" />
      </concept>
      <concept>
        <code value="OMIM:259450" />
        <display value="BRUCK SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:259500" />
        <display value="OSTEOGENIC SARCOMA" />
      </concept>
      <concept>
        <code value="OMIM:259550" />
        <display value="OSTEOID OSTEOMA" />
      </concept>
      <concept>
        <code value="OMIM:259600" />
        <display value="MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:259610" />
        <display value="OSTEOLYSIS SYNDROME, RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:259650" />
        <display value="OSTEOMA OF MIDDLE EAR" />
      </concept>
      <concept>
        <code value="OMIM:259660" />
        <display value="OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION" />
      </concept>
      <concept>
        <code value="OMIM:259680" />
        <display value="CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS" />
      </concept>
      <concept>
        <code value="OMIM:259690" />
        <display value="OSTEOPENIA AND SPARSE HAIR" />
      </concept>
      <concept>
        <code value="OMIM:259700" />
        <display value="OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1" />
      </concept>
      <concept>
        <code value="OMIM:259710" />
        <display value="OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:259720" />
        <display value="OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5" />
      </concept>
      <concept>
        <code value="OMIM:259730" />
        <display value="OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:259750" />
        <display value="OSTEOPOROSIS, JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:259770" />
        <display value="OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:259775" />
        <display value="RAINE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:259780" />
        <display value="OTOONYCHOPERONEAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:259900" />
        <display value="HYPEROXALURIA, PRIMARY, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:260000" />
        <display value="HYPEROXALURIA, PRIMARY, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:260005" />
        <display value="5-OXOPROLINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:260100" />
        <display value="PA POLYMORPHISM OF ALPHA-2-GLOBULIN" />
      </concept>
      <concept>
        <code value="OMIM:260130" />
        <display value="PACHYONYCHIA CONGENITA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:260150" />
        <display value="PALANT CLEFT PALATE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:260200" />
        <display value="PALLIDAL DEGENERATION, PROGRESSIVE, WITH RETINITIS PIGMENTOSA" />
      </concept>
      <concept>
        <code value="OMIM:260300" />
        <display value="PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:260350" />
        <display value="PANCREATIC CANCER" />
      </concept>
      <concept>
        <code value="OMIM:260370" />
        <display value="PANCREATIC AGENESIS 1" />
      </concept>
      <concept>
        <code value="OMIM:260400" />
        <display value="SHWACHMAN-DIAMOND SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:260450" />
        <display value="PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE" />
      </concept>
      <concept>
        <code value="OMIM:260470" />
        <display value="PANENCEPHALITIS, SUBACUTE SCLEROSING" />
      </concept>
      <concept>
        <code value="OMIM:260480" />
        <display value="PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX" />
      </concept>
      <concept>
        <code value="OMIM:260500" />
        <display value="PAPILLOMA OF CHOROID PLEXUS" />
      </concept>
      <concept>
        <code value="OMIM:260530" />
        <display value="PARANA HARD-SKIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:260540" />
        <display value="PARKINSON-DEMENTIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:260555" />
        <display value="PARTINGTON-ANDERSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:260565" />
        <display value="PEHO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:260570" />
        <display value="PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN" />
      </concept>
      <concept>
        <code value="OMIM:260600" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 3" />
      </concept>
      <concept>
        <code value="OMIM:260650" />
        <display value="PELLAGRA-LIKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:260660" />
        <display value="COUSIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:260800" />
        <display value="PENTOSURIA" />
      </concept>
      <concept>
        <code value="OMIM:260900" />
        <display value="PERICARDIAL EFFUSION, CHRONIC" />
      </concept>
      <concept>
        <code value="OMIM:260910" />
        <display value="PERIFOLLICULITIS CAPITIS ABSCEDENS ET SUFFODIENS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:260920" />
        <display value="HYPER-IgD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:260950" />
        <display value="PERIODONTITIS, CHRONIC" />
      </concept>
      <concept>
        <code value="OMIM:260970" />
        <display value="PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND SPONGY DEGENERATION OF BRAIN" />
      </concept>
      <concept>
        <code value="OMIM:261000" />
        <display value="INTRINSIC FACTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:261100" />
        <display value="MEGALOBLASTIC ANEMIA 1" />
      </concept>
      <concept>
        <code value="OMIM:261400" />
        <display value="PERONEUS TERTIUS MUSCLE, ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:261500" />
        <display value="EOSINOPHIL PEROXIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:261515" />
        <display value="D-BIFUNCTIONAL PROTEIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:261540" />
        <display value="PETERS-PLUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:261550" />
        <display value="PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II" />
      </concept>
      <concept>
        <code value="OMIM:261560" />
        <display value="PFEIFFER-PALM-TELLER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:261575" />
        <display value="PHAVER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:261590" />
        <display value="PHENFORMIN 4-HYDROXYLATION" />
      </concept>
      <concept>
        <code value="OMIM:261600" />
        <display value="PHENYLKETONURIA" />
      </concept>
      <concept>
        <code value="OMIM:261630" />
        <display value="HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C" />
      </concept>
      <concept>
        <code value="OMIM:261640" />
        <display value="HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A" />
      </concept>
      <concept>
        <code value="OMIM:261650" />
        <display value="PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, MITOCHONDRIAL" />
      </concept>
      <concept>
        <code value="OMIM:261670" />
        <display value="GLYCOGEN STORAGE DISEASE X" />
      </concept>
      <concept>
        <code value="OMIM:261680" />
        <display value="PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC" />
      </concept>
      <concept>
        <code value="OMIM:261740" />
        <display value="GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:261750" />
        <display value="GLYCOGEN STORAGE DISEASE IXb" />
      </concept>
      <concept>
        <code value="OMIM:261800" />
        <display value="PIERRE ROBIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:261900" />
        <display value="PILI TORTI, EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:261990" />
        <display value="PILI TORTI AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:262000" />
        <display value="BJORNSTAD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:262020" />
        <display value="PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS" />
      </concept>
      <concept>
        <code value="OMIM:262190" />
        <display value="PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:262300" />
        <display value="ACHROMATOPSIA 3" />
      </concept>
      <concept>
        <code value="OMIM:262400" />
        <display value="ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IA" />
      </concept>
      <concept>
        <code value="OMIM:262500" />
        <display value="LARON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:262600" />
        <display value="PITUITARY HORMONE DEFICIENCY, COMBINED, 2" />
      </concept>
      <concept>
        <code value="OMIM:262650" />
        <display value="KOWARSKI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:262700" />
        <display value="PITUITARY HORMONE DEFICIENCY, COMBINED, 4" />
      </concept>
      <concept>
        <code value="OMIM:262710" />
        <display value="PITUITARY DWARFISM WITH LARGE SELLA TURCICA" />
      </concept>
      <concept>
        <code value="OMIM:262800" />
        <display value="PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:262850" />
        <display value="ALPHA-2-PLASMIN INHIBITOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:262875" />
        <display value="PLATELET PROSTACYCLIN RECEPTOR DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:262890" />
        <display value="SCOTT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:262900" />
        <display value="PLEOCONIAL MYOPATHY WITH SALT CRAVING" />
      </concept>
      <concept>
        <code value="OMIM:263000" />
        <display value="INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:263100" />
        <display value="POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS" />
      </concept>
      <concept>
        <code value="OMIM:263200" />
        <display value="POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:263210" />
        <display value="GILLESSEN-KAESBACH-NISHIMURA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:263300" />
        <display value="POLYCYTHEMIA VERA" />
      </concept>
      <concept>
        <code value="OMIM:263400" />
        <display value="ERYTHROCYTOSIS, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:263450" />
        <display value="POLYDACTYLY, POSTAXIAL, TYPE A5" />
      </concept>
      <concept>
        <code value="OMIM:263520" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:263540" />
        <display value="POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:263550" />
        <display value="POLYMYOCLONUS, INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:263570" />
        <display value="POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM" />
      </concept>
      <concept>
        <code value="OMIM:263600" />
        <display value="POLYSACCHARIDE, STORAGE OF UNUSUAL" />
      </concept>
      <concept>
        <code value="OMIM:263610" />
        <display value="POLYHYDRAMNIOS, CHRONIC IDIOPATHIC" />
      </concept>
      <concept>
        <code value="OMIM:263630" />
        <display value="POLYSYNDACTYLY WITH CARDIAC MALFORMATION" />
      </concept>
      <concept>
        <code value="OMIM:263650" />
        <display value="BARTSOCAS-PAPAS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:263700" />
        <display value="PORPHYRIA, CONGENITAL ERYTHROPOIETIC" />
      </concept>
      <concept>
        <code value="OMIM:263750" />
        <display value="POSTAXIAL ACROFACIAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:263800" />
        <display value="GITELMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:264010" />
        <display value="PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:264050" />
        <display value="PRENATAL BOWING" />
      </concept>
      <concept>
        <code value="OMIM:264060" />
        <display value="PREPAPILLARY VASCULAR LOOPS" />
      </concept>
      <concept>
        <code value="OMIM:264070" />
        <display value="HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D" />
      </concept>
      <concept>
        <code value="OMIM:264080" />
        <display value="PROGESTERONE RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:264090" />
        <display value="PROGEROID SYNDROME, NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:264110" />
        <display value="PROLACTIN DEFICIENCY, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:264120" />
        <display value="PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES" />
      </concept>
      <concept>
        <code value="OMIM:264140" />
        <display value="PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:264180" />
        <display value="PSEUDODIASTROPHIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:264270" />
        <display value="PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:264300" />
        <display value="17-BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:264350" />
        <display value="PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:264420" />
        <display value="FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM" />
      </concept>
      <concept>
        <code value="OMIM:264470" />
        <display value="PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:264475" />
        <display value="PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HAND ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:264480" />
        <display value="PSEUDOTRISOMY 13 SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:264500" />
        <display value="PSEUDOURIDINURIA AND MENTAL DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:264600" />
        <display value="PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS" />
      </concept>
      <concept>
        <code value="OMIM:264700" />
        <display value="VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A" />
      </concept>
      <concept>
        <code value="OMIM:264800" />
        <display value="PSEUDOXANTHOMA ELASTICUM" />
      </concept>
      <concept>
        <code value="OMIM:265000" />
        <display value="MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT" />
      </concept>
      <concept>
        <code value="OMIM:265050" />
        <display value="3MC SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:265100" />
        <display value="PULMONARY ALVEOLAR MICROLITHIASIS" />
      </concept>
      <concept>
        <code value="OMIM:265120" />
        <display value="SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:265140" />
        <display value="PULMONARY ARTERIOVENOUS FISTULAS" />
      </concept>
      <concept>
        <code value="OMIM:265150" />
        <display value="PULMONARY ATRESIA WITH INTACT VENTRICULAR SEPTUM" />
      </concept>
      <concept>
        <code value="OMIM:265200" />
        <display value="PULMONARY BULLAE CAUSING PNEUMOTHORAX" />
      </concept>
      <concept>
        <code value="OMIM:265300" />
        <display value="LYMPHANGIECTASIA, PULMONARY, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:265380" />
        <display value="ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS" />
      </concept>
      <concept>
        <code value="OMIM:265400" />
        <display value="PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:265430" />
        <display value="LUNG AGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:265450" />
        <display value="PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:265500" />
        <display value="PULMONIC STENOSIS" />
      </concept>
      <concept>
        <code value="OMIM:265600" />
        <display value="PULMONIC STENOSIS AND CONGENITAL NEPHROSIS" />
      </concept>
      <concept>
        <code value="OMIM:265800" />
        <display value="PYCNODYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:265850" />
        <display value="PYGMY" />
      </concept>
      <concept>
        <code value="OMIM:265880" />
        <display value="PYKNOACHONDROGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:265900" />
        <display value="PYLE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:265950" />
        <display value="PYLORIC ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:266100" />
        <display value="EPILEPSY, PYRIDOXINE-DEPENDENT" />
      </concept>
      <concept>
        <code value="OMIM:266120" />
        <display value="URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:266130" />
        <display value="GLUTATHIONE SYNTHETASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:266140" />
        <display value="PYROPOIKILOCYTOSIS, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:266150" />
        <display value="PYRUVATE CARBOXYLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:266200" />
        <display value="PYRUVATE KINASE DEFICIENCY OF RED CELLS" />
      </concept>
      <concept>
        <code value="OMIM:266250" />
        <display value="RADICULONEUROPATHY, FATAL NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:266255" />
        <display value="RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATION AND HYPOTONIA" />
      </concept>
      <concept>
        <code value="OMIM:266265" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc" />
      </concept>
      <concept>
        <code value="OMIM:266270" />
        <display value="RAMON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:266280" />
        <display value="RAPADILINO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:266300" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2" />
      </concept>
      <concept>
        <code value="OMIM:266350" />
        <display value="RED SKIN PIGMENT ANOMALY OF NEW GUINEA" />
      </concept>
      <concept>
        <code value="OMIM:266400" />
        <display value="REESE RETINAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:266500" />
        <display value="REFSUM DISEASE, CLASSIC" />
      </concept>
      <concept>
        <code value="OMIM:266510" />
        <display value="PEROXISOME BIOGENESIS DISORDER 3B" />
      </concept>
      <concept>
        <code value="OMIM:266600" />
        <display value="INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 1" />
      </concept>
      <concept>
        <code value="OMIM:266810" />
        <display value="RENAL AND MULLERIAN DUCT HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:266900" />
        <display value="SENIOR-LOKEN SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:266910" />
        <display value="RENAL DYSPLASIA-LIMB DEFECTS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:266920" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:267000" />
        <display value="PERLMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:267010" />
        <display value="MECKEL SYNDROME, TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:267200" />
        <display value="RENAL TUBULAR ACIDOSIS III" />
      </concept>
      <concept>
        <code value="OMIM:267300" />
        <display value="RENAL TUBULAR ACIDOSIS, DISTAL, WITH PROGRESSIVE NERVE DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:267400" />
        <display value="RENAL, GENITAL, AND MIDDLE EAR ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:267430" />
        <display value="RENAL TUBULAR DYSGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:267450" />
        <display value="RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS" />
      </concept>
      <concept>
        <code value="OMIM:267480" />
        <display value="RESPIRATORY UNDERRESPONSIVENESS TO HYPOXIA AND HYPERCAPNIA" />
      </concept>
      <concept>
        <code value="OMIM:267500" />
        <display value="RETICULAR DYSGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:267700" />
        <display value="HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:267730" />
        <display value="RETICULUM CELL SARCOMA" />
      </concept>
      <concept>
        <code value="OMIM:267740" />
        <display value="RETINAL DEGENERATION AND EPILEPSY" />
      </concept>
      <concept>
        <code value="OMIM:267750" />
        <display value="KNOBLOCH SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:267760" />
        <display value="RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION, AND ANGLE CLOSURE GLAUCOMA" />
      </concept>
      <concept>
        <code value="OMIM:267800" />
        <display value="RETINAL DYSTROPHY, RETICULAR PIGMENTARY, OF POSTERIOR POLE" />
      </concept>
      <concept>
        <code value="OMIM:267900" />
        <display value="RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:268000" />
        <display value="RETINITIS PIGMENTOSA" />
      </concept>
      <concept>
        <code value="OMIM:268010" />
        <display value="RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:268020" />
        <display value="RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:268025" />
        <display value="RETINITIS PIGMENTOSA, LATE-ADULT ONSET" />
      </concept>
      <concept>
        <code value="OMIM:268040" />
        <display value="RETINOHEPATOENDOCRINOLOGIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268050" />
        <display value="RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:268060" />
        <display value="RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:268080" />
        <display value="RETINOSCHISIS OF FOVEA" />
      </concept>
      <concept>
        <code value="OMIM:268100" />
        <display value="ENHANCED S-CONE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268130" />
        <display value="REVESZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268150" />
        <display value="RH-NULL, REGULATOR TYPE" />
      </concept>
      <concept>
        <code value="OMIM:268200" />
        <display value="MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:268210" />
        <display value="RHABDOMYOSARCOMA, EMBRYONAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:268220" />
        <display value="RHABDOMYOSARCOMA 2" />
      </concept>
      <concept>
        <code value="OMIM:268240" />
        <display value="RHEUMATIC FEVER-RELATED ANTIGEN" />
      </concept>
      <concept>
        <code value="OMIM:268250" />
        <display value="RHIZOMELIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268300" />
        <display value="ROBERTS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268305" />
        <display value="ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:268310" />
        <display value="ROBINOW SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:268315" />
        <display value="ROD-CONE DYSTROPHY, SENSORINEURAL DEAFNESS, AND FANCONI-TYPE RENAL DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:268320" />
        <display value="RODRIGUES BLINDNESS" />
      </concept>
      <concept>
        <code value="OMIM:268400" />
        <display value="ROTHMUND-THOMSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268500" />
        <display value="ROWLEY-ROSENBERG SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268650" />
        <display value="RUDIGER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268700" />
        <display value="SACCHAROPINURIA" />
      </concept>
      <concept>
        <code value="OMIM:268800" />
        <display value="SANDHOFF DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:268850" />
        <display value="RICHIERI-COSTA/GUION-ALMEIDA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:268900" />
        <display value="SARCOSINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:269000" />
        <display value="SC PHOCOMELIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:269150" />
        <display value="SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:269160" />
        <display value="SCHIZENCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:269200" />
        <display value="AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:269250" />
        <display value="SCHNECKENBECKEN DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:269300" />
        <display value="CRANIOMETADIAPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:269400" />
        <display value="ANTERIOR SEGMENT DYSGENESIS 7" />
      </concept>
      <concept>
        <code value="OMIM:269500" />
        <display value="SCLEROSTEOSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:269600" />
        <display value="SEA-BLUE HISTIOCYTE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:269630" />
        <display value="SECOND METATARSAL-METACARPAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:269650" />
        <display value="SECRETORY COMPONENT DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:269700" />
        <display value="LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:269720" />
        <display value="SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:269800" />
        <display value="SENILE PLAQUE FORMATION" />
      </concept>
      <concept>
        <code value="OMIM:269840" />
        <display value="IMMUNODEFICIENCY 48" />
      </concept>
      <concept>
        <code value="OMIM:269860" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 12" />
      </concept>
      <concept>
        <code value="OMIM:269870" />
        <display value="SHORT STATURE-OBESITY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:269880" />
        <display value="SHORT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:269920" />
        <display value="INFANTILE SIALIC ACID STORAGE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:269921" />
        <display value="SIALURIA" />
      </concept>
      <concept>
        <code value="OMIM:270100" />
        <display value="HETEROTAXY, VISCERAL, 5, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:270150" />
        <display value="SJOGREN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:270200" />
        <display value="SJOGREN-LARSSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:270220" />
        <display value="SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT" />
      </concept>
      <concept>
        <code value="OMIM:270300" />
        <display value="PEELING SKIN SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:270350" />
        <display value="ANOSMIA FOR BUTYL MERCAPTAN" />
      </concept>
      <concept>
        <code value="OMIM:270400" />
        <display value="SMITH-LEMLI-OPITZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:270420" />
        <display value="DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:270425" />
        <display value="SODIUM-POTASSIUM-ATPase ACTIVITY OF RED CELL" />
      </concept>
      <concept>
        <code value="OMIM:270450" />
        <display value="INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO" />
      </concept>
      <concept>
        <code value="OMIM:270460" />
        <display value="SONODA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:270500" />
        <display value="ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:270550" />
        <display value="SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:270600" />
        <display value="SPASTIC DIPLEGIA AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:270685" />
        <display value="SPASTIC PARAPLEGIA 17, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:270700" />
        <display value="SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:270750" />
        <display value="SPASTIC PARAPLEGIA 23" />
      </concept>
      <concept>
        <code value="OMIM:270800" />
        <display value="SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:270805" />
        <display value="SPASTIC PARAPLEGIA WITH MYOCLONIC EPILEPSY" />
      </concept>
      <concept>
        <code value="OMIM:270850" />
        <display value="SPASTIC PARESIS, GLAUCOMA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:270900" />
        <display value="SPASTIC PSEUDOSCLEROSIS" />
      </concept>
      <concept>
        <code value="OMIM:270950" />
        <display value="SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:270960" />
        <display value="SPERMATOGENIC FAILURE 4" />
      </concept>
      <concept>
        <code value="OMIM:270970" />
        <display value="SPHEROCYTOSIS, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:271109" />
        <display value="SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:271110" />
        <display value="SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND MENTAL SUBNORMALITY" />
      </concept>
      <concept>
        <code value="OMIM:271150" />
        <display value="SPINAL MUSCULAR ATROPHY, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:271200" />
        <display value="SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:271220" />
        <display value="SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL" />
      </concept>
      <concept>
        <code value="OMIM:271225" />
        <display value="SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES" />
      </concept>
      <concept>
        <code value="OMIM:271245" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:271250" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:271270" />
        <display value="SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:271310" />
        <display value="SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:271320" />
        <display value="SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITAL CATARACTS, AND MYOPIA" />
      </concept>
      <concept>
        <code value="OMIM:271322" />
        <display value="SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS" />
      </concept>
      <concept>
        <code value="OMIM:271400" />
        <display value="ASPLENIA, ISOLATED CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:271500" />
        <display value="SPLENOPORTAL VASCULAR ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:271510" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE" />
      </concept>
      <concept>
        <code value="OMIM:271520" />
        <display value="SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:271530" />
        <display value="BRACHYOLMIA TYPE 1, HOBAEK TYPE" />
      </concept>
      <concept>
        <code value="OMIM:271600" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:271620" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:271630" />
        <display value="BRACHYOLMIA TYPE 1, TOLEDO TYPE" />
      </concept>
      <concept>
        <code value="OMIM:271640" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES" />
      </concept>
      <concept>
        <code value="OMIM:271650" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:271665" />
        <display value="SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE" />
      </concept>
      <concept>
        <code value="OMIM:271700" />
        <display value="SPONDYLOPERIPHERAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:271900" />
        <display value="CANAVAN DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:271930" />
        <display value="STRIATONIGRAL DEGENERATION, INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:271950" />
        <display value="SUBAORTIC STENOSIS, MEMBRANOUS" />
      </concept>
      <concept>
        <code value="OMIM:271960" />
        <display value="SUBAORTIC STENOSIS--SHORT STATURE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:271980" />
        <display value="SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:272000" />
        <display value="SUCROSURIA, HIATUS HERNIA AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:272100" />
        <display value="SUDANOPHILIC CEREBRAL SCLEROSIS" />
      </concept>
      <concept>
        <code value="OMIM:272120" />
        <display value="SUDDEN INFANT DEATH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:272150" />
        <display value="SUGARMAN BRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:272200" />
        <display value="MULTIPLE SULFATASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:272300" />
        <display value="SULFITE OXIDASE DEFICIENCY, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:272350" />
        <display value="SUMMITT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:272370" />
        <display value="SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS" />
      </concept>
      <concept>
        <code value="OMIM:272430" />
        <display value="CRISPONI/COLD-INDUCED SWEATING SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:272440" />
        <display value="FILIPPI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:272450" />
        <display value="SYNDESMODYSPLASIC DWARFISM" />
      </concept>
      <concept>
        <code value="OMIM:272460" />
        <display value="SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:272600" />
        <display value="TAPETORETINAL DEGENERATION WITH ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:272620" />
        <display value="TARDIVE DYSKINESIA" />
      </concept>
      <concept>
        <code value="OMIM:272650" />
        <display value="TATSUMI FACTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:272700" />
        <display value="TAURODONTISM" />
      </concept>
      <concept>
        <code value="OMIM:272750" />
        <display value="GM2-GANGLIOSIDOSIS, AB VARIANT" />
      </concept>
      <concept>
        <code value="OMIM:272800" />
        <display value="TAY-SACHS DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:272950" />
        <display value="TEEBI-SHALTOUT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:272980" />
        <display value="TEETH, CONGENITAL ABSENCE OF, WITH TAURODONTIA AND SPARSE HAIR" />
      </concept>
      <concept>
        <code value="OMIM:273000" />
        <display value="TEETH, FUSED" />
      </concept>
      <concept>
        <code value="OMIM:273050" />
        <display value="TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM" />
      </concept>
      <concept>
        <code value="OMIM:273120" />
        <display value="TERATOMA, PINEAL" />
      </concept>
      <concept>
        <code value="OMIM:273150" />
        <display value="TESTES, RUDIMENTARY" />
      </concept>
      <concept>
        <code value="OMIM:273250" />
        <display value="TESTICULAR REGRESSION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:273300" />
        <display value="TESTICULAR GERM CELL TUMOR" />
      </concept>
      <concept>
        <code value="OMIM:273390" />
        <display value="TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:273395" />
        <display value="TETRAAMELIA SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:273400" />
        <display value="TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, AND OTHER ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:273490" />
        <display value="THALAMIC DEGENERATION, SYMMETRIC INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:273600" />
        <display value="THALIDOMIDE SUSCEPTIBILITY" />
      </concept>
      <concept>
        <code value="OMIM:273680" />
        <display value="THANATOPHORIC DYSPLASIA, GLASGOW VARIANT" />
      </concept>
      <concept>
        <code value="OMIM:273730" />
        <display value="THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:273740" />
        <display value="THORACOMELIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:273750" />
        <display value="THREE M SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:273770" />
        <display value="THREONINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:273800" />
        <display value="GLANZMANN THROMBASTHENIA" />
      </concept>
      <concept>
        <code value="OMIM:273900" />
        <display value="THROMBOCYTOPENIA 3" />
      </concept>
      <concept>
        <code value="OMIM:274000" />
        <display value="THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:274150" />
        <display value="THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:274190" />
        <display value="THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:274200" />
        <display value="THUMB, DISTAL HYPEREXTENSIBILITY OF" />
      </concept>
      <concept>
        <code value="OMIM:274205" />
        <display value="THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:274210" />
        <display value="THYMIC APLASIA WITH FETAL DEATH" />
      </concept>
      <concept>
        <code value="OMIM:274230" />
        <display value="THYMOMA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:274240" />
        <display value="THYROCEREBRORETINAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:274265" />
        <display value="THYMIC-RENAL-ANAL-LUNG DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:274270" />
        <display value="DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:274300" />
        <display value="THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:274400" />
        <display value="THYROID DYSHORMONOGENESIS 1" />
      </concept>
      <concept>
        <code value="OMIM:274500" />
        <display value="THYROID DYSHORMONOGENESIS 2A" />
      </concept>
      <concept>
        <code value="OMIM:274600" />
        <display value="PENDRED SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:274700" />
        <display value="THYROID DYSHORMONOGENESIS 3" />
      </concept>
      <concept>
        <code value="OMIM:274800" />
        <display value="THYROID DYSHORMONOGENESIS 4" />
      </concept>
      <concept>
        <code value="OMIM:274900" />
        <display value="THYROID DYSHORMONOGENESIS 5" />
      </concept>
      <concept>
        <code value="OMIM:275000" />
        <display value="GRAVES DISEASE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:275100" />
        <display value="HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4" />
      </concept>
      <concept>
        <code value="OMIM:275120" />
        <display value="THYROTROPIN-RELEASING HORMONE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:275190" />
        <display value="TIGLIC ACIDEMIA" />
      </concept>
      <concept>
        <code value="OMIM:275200" />
        <display value="HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1" />
      </concept>
      <concept>
        <code value="OMIM:275210" />
        <display value="RESTRICTIVE DERMOPATHY, LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:275220" />
        <display value="TIBIAL HEMIMELIA" />
      </concept>
      <concept>
        <code value="OMIM:275230" />
        <display value="TIBIA, ABSENCE OF, WITH CONGENITAL DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:275240" />
        <display value="TINEA IMBRICATA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:275250" />
        <display value="TONGUE, PIGMENTED FUNGIFORM PAPILLAE OF" />
      </concept>
      <concept>
        <code value="OMIM:275300" />
        <display value="TRACHEOBRONCHOMEGALY" />
      </concept>
      <concept>
        <code value="OMIM:275350" />
        <display value="TRANSCOBALAMIN II DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:275355" />
        <display value="SQUAMOUS CELL CARCINOMA, HEAD AND NECK" />
      </concept>
      <concept>
        <code value="OMIM:275370" />
        <display value="TRICARBOXYLIC ACID CYCLE, DEFECT OF" />
      </concept>
      <concept>
        <code value="OMIM:275400" />
        <display value="OLIVER-MCFARLANE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:275450" />
        <display value="TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:275595" />
        <display value="TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIES OF THE HANDS AND FEET" />
      </concept>
      <concept>
        <code value="OMIM:275630" />
        <display value="CHANARIN-DORFMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:275900" />
        <display value="SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:276100" />
        <display value="TRYPTOPHANURIA WITH DWARFISM" />
      </concept>
      <concept>
        <code value="OMIM:276200" />
        <display value="T-SUBSTANCE ANOMALY" />
      </concept>
      <concept>
        <code value="OMIM:276300" />
        <display value="MISMATCH REPAIR CANCER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:276400" />
        <display value="TWINNING, DIZYGOTIC" />
      </concept>
      <concept>
        <code value="OMIM:276410" />
        <display value="TWINNING, MONOZYGOTIC" />
      </concept>
      <concept>
        <code value="OMIM:276600" />
        <display value="TYROSINEMIA, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:276700" />
        <display value="TYROSINEMIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:276710" />
        <display value="TYROSINEMIA, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:276800" />
        <display value="TYROSINOSIS" />
      </concept>
      <concept>
        <code value="OMIM:276820" />
        <display value="ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:276821" />
        <display value="ULNAR HYPOPLASIA WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:276822" />
        <display value="ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:276880" />
        <display value="UROCANASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:276900" />
        <display value="USHER SYNDROME, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:276901" />
        <display value="USHER SYNDROME, TYPE IIA" />
      </concept>
      <concept>
        <code value="OMIM:276902" />
        <display value="USHER SYNDROME, TYPE IIIA" />
      </concept>
      <concept>
        <code value="OMIM:276904" />
        <display value="USHER SYNDROME, TYPE IC" />
      </concept>
      <concept>
        <code value="OMIM:276950" />
        <display value="VACTERL ASSOCIATION WITH HYDROCEPHALUS" />
      </concept>
      <concept>
        <code value="OMIM:277000" />
        <display value="MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:277100" />
        <display value="VALINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:277150" />
        <display value="VAN BOGAERT-HOZAY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:277170" />
        <display value="OROFACIODIGITAL SYNDROME VI" />
      </concept>
      <concept>
        <code value="OMIM:277175" />
        <display value="VASCULAR HYALINOSIS" />
      </concept>
      <concept>
        <code value="OMIM:277180" />
        <display value="VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF" />
      </concept>
      <concept>
        <code value="OMIM:277200" />
        <display value="RIGHT VENTRICULAR HYPOPLASIA, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:277300" />
        <display value="SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:277320" />
        <display value="VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA" />
      </concept>
      <concept>
        <code value="OMIM:277350" />
        <display value="HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:277380" />
        <display value="METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE" />
      </concept>
      <concept>
        <code value="OMIM:277400" />
        <display value="METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE" />
      </concept>
      <concept>
        <code value="OMIM:277410" />
        <display value="METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblD TYPE" />
      </concept>
      <concept>
        <code value="OMIM:277440" />
        <display value="VITAMIN D-DEPENDENT RICKETS, TYPE 2A" />
      </concept>
      <concept>
        <code value="OMIM:277450" />
        <display value="VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1" />
      </concept>
      <concept>
        <code value="OMIM:277460" />
        <display value="VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:277465" />
        <display value="VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION" />
      </concept>
      <concept>
        <code value="OMIM:277470" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 2A" />
      </concept>
      <concept>
        <code value="OMIM:277480" />
        <display value="VON WILLEBRAND DISEASE, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:277580" />
        <display value="WAARDENBURG SYNDROME, TYPE 4A" />
      </concept>
      <concept>
        <code value="OMIM:277590" />
        <display value="WEAVER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:277600" />
        <display value="WEILL-MARCHESANI SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:277700" />
        <display value="WERNER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:277720" />
        <display value="WHISTLING FACE SYNDROME, RECESSIVE FORM" />
      </concept>
      <concept>
        <code value="OMIM:277730" />
        <display value="WERNICKE-KORSAKOFF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:277740" />
        <display value="WHITE FORELOCK WITH MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:277900" />
        <display value="WILSON DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:277950" />
        <display value="WINCHESTER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:277990" />
        <display value="WOLFF MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:278000" />
        <display value="LYSOSOMAL ACID LIPASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:278100" />
        <display value="WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:278150" />
        <display value="HYPOTRICHOSIS 8" />
      </concept>
      <concept>
        <code value="OMIM:278200" />
        <display value="WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS" />
      </concept>
      <concept>
        <code value="OMIM:278250" />
        <display value="WRINKLY SKIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:278300" />
        <display value="XANTHINURIA, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:278700" />
        <display value="XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A" />
      </concept>
      <concept>
        <code value="OMIM:278720" />
        <display value="XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C" />
      </concept>
      <concept>
        <code value="OMIM:278730" />
        <display value="XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D" />
      </concept>
      <concept>
        <code value="OMIM:278740" />
        <display value="XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E" />
      </concept>
      <concept>
        <code value="OMIM:278750" />
        <display value="XERODERMA PIGMENTOSUM, VARIANT TYPE" />
      </concept>
      <concept>
        <code value="OMIM:278760" />
        <display value="XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F" />
      </concept>
      <concept>
        <code value="OMIM:278780" />
        <display value="XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G" />
      </concept>
      <concept>
        <code value="OMIM:278800" />
        <display value="DE SANCTIS-CACCHIONE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:278850" />
        <display value="46,XX SEX REVERSAL 2" />
      </concept>
      <concept>
        <code value="OMIM:278900" />
        <display value="XYLOSIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:279000" />
        <display value="YOUNG SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:280000" />
        <display value="COLOBOMA, CONGENITAL HEART DISEASE, ICHTHYOSIFORM DERMATOSIS, MENTAL RETARDATION, AND EAR ANOMALIES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300000" />
        <display value="OPITZ GBBB SYNDROME, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:300001" />
        <display value="ICHTHYOSIS, X-LINKED, WITHOUT STEROID SULFATASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:300004" />
        <display value="CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA" />
      </concept>
      <concept>
        <code value="OMIM:300009" />
        <display value="DENT DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:300018" />
        <display value="46,XY SEX REVERSAL 2" />
      </concept>
      <concept>
        <code value="OMIM:300029" />
        <display value="RETINITIS PIGMENTOSA 3" />
      </concept>
      <concept>
        <code value="OMIM:300030" />
        <display value="DEAFNESS, X-LINKED 3" />
      </concept>
      <concept>
        <code value="OMIM:300042" />
        <display value="ALOPECIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:300046" />
        <display value="MENTAL RETARDATION, X-LINKED 23" />
      </concept>
      <concept>
        <code value="OMIM:300047" />
        <display value="MENTAL RETARDATION, X-LINKED 20" />
      </concept>
      <concept>
        <code value="OMIM:300048" />
        <display value="INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300049" />
        <display value="PERIVENTRICULAR NODULAR HETEROTOPIA 1" />
      </concept>
      <concept>
        <code value="OMIM:300054" />
        <display value="BODY LENGTH, MOUSE, HUMAN HOMOLOG" />
      </concept>
      <concept>
        <code value="OMIM:300055" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 13" />
      </concept>
      <concept>
        <code value="OMIM:300062" />
        <display value="MENTAL RETARDATION, X-LINKED 14" />
      </concept>
      <concept>
        <code value="OMIM:300064" />
        <display value="MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:300066" />
        <display value="DEAFNESS, X-LINKED 4" />
      </concept>
      <concept>
        <code value="OMIM:300067" />
        <display value="LISSENCEPHALY, X-LINKED, 1" />
      </concept>
      <concept>
        <code value="OMIM:300068" />
        <display value="ANDROGEN INSENSITIVITY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300071" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A" />
      </concept>
      <concept>
        <code value="OMIM:300073" />
        <display value="FETAL AKINESIA SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300076" />
        <display value="IMMUNONEUROLOGIC DISORDER, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300082" />
        <display value="COGNITIVE FUNCTION 1, SOCIAL" />
      </concept>
      <concept>
        <code value="OMIM:300085" />
        <display value="CONE-ROD DYSTROPHY, X-LINKED, 2" />
      </concept>
      <concept>
        <code value="OMIM:300087" />
        <display value="X INACTIVATION, FAMILIAL SKEWED, 1" />
      </concept>
      <concept>
        <code value="OMIM:300088" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9" />
      </concept>
      <concept>
        <code value="OMIM:300100" />
        <display value="ADRENOLEUKODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:300106" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300113" />
        <display value="X-LINKED B CELL SURFACE ANTIGEN, MOUSE, HOMOLOG-LIKE 1" />
      </concept>
      <concept>
        <code value="OMIM:300114" />
        <display value="RAYNAUD-CLAES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300115" />
        <display value="MENTAL RETARDATION, X-LINKED 50" />
      </concept>
      <concept>
        <code value="OMIM:300123" />
        <display value="MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISM" />
      </concept>
      <concept>
        <code value="OMIM:300125" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:300129" />
        <display value="HEMATOPOIETIC STEM CELL KINETICS, CONTROL OF" />
      </concept>
      <concept>
        <code value="OMIM:300136" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:300143" />
        <display value="MENTAL RETARDATION, X-LINKED 21" />
      </concept>
      <concept>
        <code value="OMIM:300147" />
        <display value="PROSTATE CANCER, HEREDITARY, X-LINKED 1" />
      </concept>
      <concept>
        <code value="OMIM:300148" />
        <display value="MEHMO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300155" />
        <display value="RETINITIS PIGMENTOSA 24" />
      </concept>
      <concept>
        <code value="OMIM:300158" />
        <display value="ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300166" />
        <display value="MICROPHTHALMIA, SYNDROMIC 2" />
      </concept>
      <concept>
        <code value="OMIM:300179" />
        <display value="X INACTIVATION, FAMILIAL SKEWED, 2" />
      </concept>
      <concept>
        <code value="OMIM:300184" />
        <display value="HYPOTONIA, CONGENITAL NYSTAGMUS, ATAXIA, AND ABNORMAL AUDITORY BRAINSTEM RESPONSES" />
      </concept>
      <concept>
        <code value="OMIM:300194" />
        <display value="AMME COMPLEX" />
      </concept>
      <concept>
        <code value="OMIM:300200" />
        <display value="ADRENAL HYPOPLASIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:300209" />
        <display value="SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:300210" />
        <display value="MENTAL RETARDATION, X-LINKED 58" />
      </concept>
      <concept>
        <code value="OMIM:300211" />
        <display value="EPISODIC MUSCLE WEAKNESS, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300215" />
        <display value="LISSENCEPHALY, X-LINKED, 2" />
      </concept>
      <concept>
        <code value="OMIM:300216" />
        <display value="COATS DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:300218" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 7" />
      </concept>
      <concept>
        <code value="OMIM:300219" />
        <display value="MYOTUBULAR MYOPATHY WITH ABNORMAL GENITAL DEVELOPMENT" />
      </concept>
      <concept>
        <code value="OMIM:300221" />
        <display value="LYMPHOMA, HODGKIN, X-LINKED PSEUDOAUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:300228" />
        <display value="TESTICULAR GERM CELL TUMOR 1" />
      </concept>
      <concept>
        <code value="OMIM:300232" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION" />
      </concept>
      <concept>
        <code value="OMIM:300233" />
        <display value="RADIOULNAR SYNOSTOSIS, RADIAL RAY ABNORMALITIES, AND SEVERE MALFORMATIONS IN THE MALE" />
      </concept>
      <concept>
        <code value="OMIM:300238" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 11" />
      </concept>
      <concept>
        <code value="OMIM:300243" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300244" />
        <display value="TERMINAL OSSEOUS DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:300245" />
        <display value="PTOSIS, HEREDITARY CONGENITAL 2" />
      </concept>
      <concept>
        <code value="OMIM:300257" />
        <display value="DANON DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:300259" />
        <display value="MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300260" />
        <display value="LUBS X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300261" />
        <display value="ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300262" />
        <display value="ABIDI X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300263" />
        <display value="SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300266" />
        <display value="SPASTIC PARAPLEGIA 16, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300270" />
        <display value="ADRENOMYODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:300271" />
        <display value="MENTAL RETARDATION, X-LINKED 72" />
      </concept>
      <concept>
        <code value="OMIM:300273" />
        <display value="GOITER, MULTINODULAR 2" />
      </concept>
      <concept>
        <code value="OMIM:300280" />
        <display value="URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300291" />
        <display value="ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 1" />
      </concept>
      <concept>
        <code value="OMIM:300299" />
        <display value="NEUTROPENIA, SEVERE CONGENITAL, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300301" />
        <display value="ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY, OSTEOPETROSIS, AND LYMPHEDEMA" />
      </concept>
      <concept>
        <code value="OMIM:300306" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11" />
      </concept>
      <concept>
        <code value="OMIM:300310" />
        <display value="AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:300321" />
        <display value="FG SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:300322" />
        <display value="LESCH-NYHAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300323" />
        <display value="KELLEY-SEEGMILLER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300324" />
        <display value="MENTAL RETARDATION, X-LINKED 53" />
      </concept>
      <concept>
        <code value="OMIM:300331" />
        <display value="THROMBOCYTHEMIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300337" />
        <display value="HYPOMELANOSIS OF ITO" />
      </concept>
      <concept>
        <code value="OMIM:300345" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 1" />
      </concept>
      <concept>
        <code value="OMIM:300351" />
        <display value="GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1" />
      </concept>
      <concept>
        <code value="OMIM:300352" />
        <display value="CEREBRAL CREATINE DEFICIENCY SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:300354" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300355" />
        <display value="MENTAL RETARDATION, X-LINKED 73" />
      </concept>
      <concept>
        <code value="OMIM:300367" />
        <display value="THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA" />
      </concept>
      <concept>
        <code value="OMIM:300372" />
        <display value="MENTAL RETARDATION, X-LINKED 42" />
      </concept>
      <concept>
        <code value="OMIM:300373" />
        <display value="OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS" />
      </concept>
      <concept>
        <code value="OMIM:300376" />
        <display value="MUSCULAR DYSTROPHY, BECKER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300378" />
        <display value="RADIAL RAY DEFICIENCY, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300387" />
        <display value="MENTAL RETARDATION, X-LINKED 63" />
      </concept>
      <concept>
        <code value="OMIM:300388" />
        <display value="POLYMICROGYRIA, BILATERAL PERISYLVIAN, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300400" />
        <display value="SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300406" />
        <display value="FG SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:300419" />
        <display value="MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:300422" />
        <display value="FG SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:300423" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300424" />
        <display value="RETINITIS PIGMENTOSA 23" />
      </concept>
      <concept>
        <code value="OMIM:300425" />
        <display value="AUTISM, SUSCEPTIBILITY TO, X-LINKED 1" />
      </concept>
      <concept>
        <code value="OMIM:300428" />
        <display value="MENTAL RETARDATION, X-LINKED 2" />
      </concept>
      <concept>
        <code value="OMIM:300431" />
        <display value="ATKIN-FLAITZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300433" />
        <display value="MENTAL RETARDATION, X-LINKED 81" />
      </concept>
      <concept>
        <code value="OMIM:300434" />
        <display value="STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300436" />
        <display value="MENTAL RETARDATION, X-LINKED 46" />
      </concept>
      <concept>
        <code value="OMIM:300438" />
        <display value="HSD10 MITOCHONDRIAL DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:300448" />
        <display value="ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300454" />
        <display value="MENTAL RETARDATION, X-LINKED 77" />
      </concept>
      <concept>
        <code value="OMIM:300455" />
        <display value="RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITH OR WITHOUT DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:300464" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:300471" />
        <display value="CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES" />
      </concept>
      <concept>
        <code value="OMIM:300472" />
        <display value="CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA, AND MICROGNATHIA" />
      </concept>
      <concept>
        <code value="OMIM:300475" />
        <display value="DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION" />
      </concept>
      <concept>
        <code value="OMIM:300476" />
        <display value="CONE-ROD DYSTROPHY, X-LINKED, 3" />
      </concept>
      <concept>
        <code value="OMIM:300484" />
        <display value="OROFACIODIGITAL SYNDROME VIII" />
      </concept>
      <concept>
        <code value="OMIM:300486" />
        <display value="MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE" />
      </concept>
      <concept>
        <code value="OMIM:300488" />
        <display value="MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:300489" />
        <display value="SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3" />
      </concept>
      <concept>
        <code value="OMIM:300491" />
        <display value="EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIOR DISORDERS" />
      </concept>
      <concept>
        <code value="OMIM:300494" />
        <display value="ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:300495" />
        <display value="AUTISM, SUSCEPTIBILITY TO, X-LINKED 2" />
      </concept>
      <concept>
        <code value="OMIM:300496" />
        <display value="AUTISM, SUSCEPTIBILITY TO, X-LINKED 3" />
      </concept>
      <concept>
        <code value="OMIM:300497" />
        <display value="ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:300498" />
        <display value="MENTAL RETARDATION, X-LINKED 45" />
      </concept>
      <concept>
        <code value="OMIM:300500" />
        <display value="ALBINISM, OCULAR, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:300504" />
        <display value="MENTAL RETARDATION, X-LINKED 52" />
      </concept>
      <concept>
        <code value="OMIM:300505" />
        <display value="MENTAL RETARDATION, X-LINKED 84" />
      </concept>
      <concept>
        <code value="OMIM:300509" />
        <display value="DYSLEXIA, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:300510" />
        <display value="OVARIAN DYSGENESIS 2" />
      </concept>
      <concept>
        <code value="OMIM:300511" />
        <display value="PREMATURE OVARIAN FAILURE 2A" />
      </concept>
      <concept>
        <code value="OMIM:300514" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP B" />
      </concept>
      <concept>
        <code value="OMIM:300518" />
        <display value="MENTAL RETARDATION, X-LINKED 82" />
      </concept>
      <concept>
        <code value="OMIM:300519" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300523" />
        <display value="ALLAN-HERNDON-DUDLEY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300534" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300536" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:300539" />
        <display value="NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS" />
      </concept>
      <concept>
        <code value="OMIM:300554" />
        <display value="HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:300555" />
        <display value="DENT DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:300557" />
        <display value="PARKINSON DISEASE 12" />
      </concept>
      <concept>
        <code value="OMIM:300558" />
        <display value="MENTAL RETARDATION, X-LINKED 30" />
      </concept>
      <concept>
        <code value="OMIM:300559" />
        <display value="GLYCOGEN STORAGE DISEASE, TYPE IXd" />
      </concept>
      <concept>
        <code value="OMIM:300577" />
        <display value="MENTAL RETARDATION, X-LINKED 91" />
      </concept>
      <concept>
        <code value="OMIM:300578" />
        <display value="CHROMOSOME Xp11.3 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300580" />
        <display value="MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300581" />
        <display value="FG SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:300582" />
        <display value="SHORT STATURE, IDIOPATHIC, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300584" />
        <display value="IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:300589" />
        <display value="NYSTAGMUS 5, CONGENITAL, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300590" />
        <display value="CORNELIA DE LANGE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:300591" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 6" />
      </concept>
      <concept>
        <code value="OMIM:300600" />
        <display value="ALAND ISLAND EYE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:300602" />
        <display value="CLARK-BARAITSER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300604" />
        <display value="PREMATURE OVARIAN FAILURE 2B" />
      </concept>
      <concept>
        <code value="OMIM:300605" />
        <display value="RETINITIS PIGMENTOSA 34" />
      </concept>
      <concept>
        <code value="OMIM:300607" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8" />
      </concept>
      <concept>
        <code value="OMIM:300612" />
        <display value="BROOKS-WISNIEWSKI-BROWN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300613" />
        <display value="MYOPIA 13, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300614" />
        <display value="DEAFNESS, X-LINKED 5" />
      </concept>
      <concept>
        <code value="OMIM:300615" />
        <display value="BRUNNER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300619" />
        <display value="CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:300622" />
        <display value="TN POLYAGGLUTINATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300623" />
        <display value="FRAGILE X TREMOR/ATAXIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300624" />
        <display value="FRAGILE X SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300633" />
        <display value="HYPOSPADIAS 1, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300635" />
        <display value="LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2" />
      </concept>
      <concept>
        <code value="OMIM:300636" />
        <display value="IMMUNODEFICIENCY 33" />
      </concept>
      <concept>
        <code value="OMIM:300640" />
        <display value="INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2" />
      </concept>
      <concept>
        <code value="OMIM:300643" />
        <display value="ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300645" />
        <display value="IMMUNODEFICIENCY 34" />
      </concept>
      <concept>
        <code value="OMIM:300650" />
        <display value="ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:300652" />
        <display value="ANGIOMA SERPIGINOSUM, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300653" />
        <display value="PHOSPHOGLYCERATE KINASE 1 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:300659" />
        <display value="MENTAL RETARDATION, X-LINKED 93" />
      </concept>
      <concept>
        <code value="OMIM:300660" />
        <display value="LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:300661" />
        <display value="PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY" />
      </concept>
      <concept>
        <code value="OMIM:300672" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2" />
      </concept>
      <concept>
        <code value="OMIM:300673" />
        <display value="ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS" />
      </concept>
      <concept>
        <code value="OMIM:300676" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 14" />
      </concept>
      <concept>
        <code value="OMIM:300679" />
        <display value="CHROMOSOME Xp21 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300695" />
        <display value="SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:300696" />
        <display value="MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:300699" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300700" />
        <display value="ALBINISM-DEAFNESS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300703" />
        <display value="SPINOCEREBELLAR ATAXIA, X-LINKED 5" />
      </concept>
      <concept>
        <code value="OMIM:300704" />
        <display value="PROSTATE CANCER, HEREDITARY, X-LINKED 2" />
      </concept>
      <concept>
        <code value="OMIM:300705" />
        <display value="CHROMOSOME Xp11.22 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300706" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300707" />
        <display value="TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:300709" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 9" />
      </concept>
      <concept>
        <code value="OMIM:300710" />
        <display value="ALOPECIA, ANDROGENETIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:300711" />
        <display value="PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 4" />
      </concept>
      <concept>
        <code value="OMIM:300712" />
        <display value="CRANIOFACIOSKELETAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300716" />
        <display value="MENTAL RETARDATION, X-LINKED 95" />
      </concept>
      <concept>
        <code value="OMIM:300717" />
        <display value="REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET" />
      </concept>
      <concept>
        <code value="OMIM:300718" />
        <display value="REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET" />
      </concept>
      <concept>
        <code value="OMIM:300719" />
        <display value="DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:300749" />
        <display value="MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:300750" />
        <display value="SPASTIC PARAPLEGIA 34, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300751" />
        <display value="ANEMIA, SIDEROBLASTIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:300752" />
        <display value="PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300755" />
        <display value="AGAMMAGLOBULINEMIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300756" />
        <display value="ALZHEIMER DISEASE 16" />
      </concept>
      <concept>
        <code value="OMIM:300758" />
        <display value="HYPOSPADIAS 2, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300770" />
        <display value="SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4" />
      </concept>
      <concept>
        <code value="OMIM:300778" />
        <display value="CORNEAL DYSTROPHY, LISCH EPITHELIAL" />
      </concept>
      <concept>
        <code value="OMIM:300779" />
        <display value="CORNEAL DYSTROPHY, ENDOTHELIAL, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300799" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300801" />
        <display value="CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300802" />
        <display value="MENTAL RETARDATION, X-LINKED 96" />
      </concept>
      <concept>
        <code value="OMIM:300803" />
        <display value="MENTAL RETARDATION, X-LINKED 97" />
      </concept>
      <concept>
        <code value="OMIM:300804" />
        <display value="JOUBERT SYNDROME 10" />
      </concept>
      <concept>
        <code value="OMIM:300807" />
        <display value="THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:300809" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 15" />
      </concept>
      <concept>
        <code value="OMIM:300813" />
        <display value="SARCOMA, SYNOVIAL" />
      </concept>
      <concept>
        <code value="OMIM:300814" />
        <display value="NYSTAGMUS 6, CONGENITAL, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300815" />
        <display value="CHROMOSOME Xq28 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300816" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6" />
      </concept>
      <concept>
        <code value="OMIM:300818" />
        <display value="PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1" />
      </concept>
      <concept>
        <code value="OMIM:300829" />
        <display value="CARDIOMYOPATHY, FATAL FETAL, DUE TO MYOCARDIAL CALCIFICATION" />
      </concept>
      <concept>
        <code value="OMIM:300830" />
        <display value="AUTISM, SUSCEPTIBILITY TO, X-LINKED 4" />
      </concept>
      <concept>
        <code value="OMIM:300831" />
        <display value="CK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300833" />
        <display value="46,XX SEX REVERSAL 3" />
      </concept>
      <concept>
        <code value="OMIM:300834" />
        <display value="MACULAR DEGENERATION, X-LINKED ATROPHIC" />
      </concept>
      <concept>
        <code value="OMIM:300835" />
        <display value="ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:300842" />
        <display value="MCLEOD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300843" />
        <display value="BORNHOLM EYE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:300844" />
        <display value="MENTAL RETARDATION, X-LINKED 19" />
      </concept>
      <concept>
        <code value="OMIM:300845" />
        <display value="MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:300847" />
        <display value="AUTISM, SUSCEPTIBILITY TO, X-LINKED 5" />
      </concept>
      <concept>
        <code value="OMIM:300848" />
        <display value="MENTAL RETARDATION, X-LINKED 89" />
      </concept>
      <concept>
        <code value="OMIM:300849" />
        <display value="MENTAL RETARDATION, X-LINKED 41" />
      </concept>
      <concept>
        <code value="OMIM:300850" />
        <display value="MENTAL RETARDATION, X-LINKED 90" />
      </concept>
      <concept>
        <code value="OMIM:300851" />
        <display value="MENTAL RETARDATION, X-LINKED 92" />
      </concept>
      <concept>
        <code value="OMIM:300852" />
        <display value="MENTAL RETARDATION, X-LINKED 88" />
      </concept>
      <concept>
        <code value="OMIM:300853" />
        <display value="IMMUNODEFICIENCY, X-LINKED, WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUS INFECTION, AND NEOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:300854" />
        <display value="RENAL CELL CARCINOMA, Xp11-ASSOCIATED" />
      </concept>
      <concept>
        <code value="OMIM:300855" />
        <display value="OGDEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300856" />
        <display value="HYPOSPADIAS 4, X-LINKED, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:300857" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:300858" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 17" />
      </concept>
      <concept>
        <code value="OMIM:300860" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300861" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300863" />
        <display value="CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA" />
      </concept>
      <concept>
        <code value="OMIM:300864" />
        <display value="CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300867" />
        <display value="KABUKI SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:300868" />
        <display value="MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:300869" />
        <display value="CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300870" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 5" />
      </concept>
      <concept>
        <code value="OMIM:300872" />
        <display value="AUTISM, SUSCEPTIBILITY TO, X-LINKED 6" />
      </concept>
      <concept>
        <code value="OMIM:300881" />
        <display value="BARATELA-SCOTT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300882" />
        <display value="CORNELIA DE LANGE SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:300884" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36" />
      </concept>
      <concept>
        <code value="OMIM:300886" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 32" />
      </concept>
      <concept>
        <code value="OMIM:300887" />
        <display value="LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2" />
      </concept>
      <concept>
        <code value="OMIM:300888" />
        <display value="HYPOTHYROIDISM, CENTRAL, AND TESTICULAR ENLARGEMENT" />
      </concept>
      <concept>
        <code value="OMIM:300894" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5" />
      </concept>
      <concept>
        <code value="OMIM:300895" />
        <display value="OHDO SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300896" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm" />
      </concept>
      <concept>
        <code value="OMIM:300905" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6" />
      </concept>
      <concept>
        <code value="OMIM:300908" />
        <display value="ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:300909" />
        <display value="ANGIOEDEMA INDUCED BY ACE INHIBITORS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:300910" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18" />
      </concept>
      <concept>
        <code value="OMIM:300911" />
        <display value="PARKINSONISM WITH SPASTICITY, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300912" />
        <display value="MENTAL RETARDATION, X-LINKED 98" />
      </concept>
      <concept>
        <code value="OMIM:300914" />
        <display value="DEAFNESS, X-LINKED 6" />
      </concept>
      <concept>
        <code value="OMIM:300915" />
        <display value="MICROPHTHALMIA, SYNDROMIC 13" />
      </concept>
      <concept>
        <code value="OMIM:300918" />
        <display value="PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300919" />
        <display value="MENTAL RETARDATION, X-LINKED 99" />
      </concept>
      <concept>
        <code value="OMIM:300923" />
        <display value="MENTAL RETARDATION, X-LINKED 100" />
      </concept>
      <concept>
        <code value="OMIM:300928" />
        <display value="MENTAL RETARDATION, X-LINKED 101" />
      </concept>
      <concept>
        <code value="OMIM:300932" />
        <display value="THYROXINE-BINDING GLOBULIN QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:300934" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iy" />
      </concept>
      <concept>
        <code value="OMIM:300942" />
        <display value="CHROMOSOME Xq26.3 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300943" />
        <display value="PITUITARY ADENOMA 2, GROWTH HORMONE-SECRETING" />
      </concept>
      <concept>
        <code value="OMIM:300946" />
        <display value="DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:300952" />
        <display value="LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3" />
      </concept>
      <concept>
        <code value="OMIM:300953" />
        <display value="TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:300957" />
        <display value="MENTAL RETARDATION, X-LINKED 12" />
      </concept>
      <concept>
        <code value="OMIM:300958" />
        <display value="MENTAL RETARDATION, X-LINKED 102" />
      </concept>
      <concept>
        <code value="OMIM:300960" />
        <display value="MEND SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300963" />
        <display value="RITSCHER-SCHINZEL SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:300966" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 33" />
      </concept>
      <concept>
        <code value="OMIM:300967" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 34" />
      </concept>
      <concept>
        <code value="OMIM:300968" />
        <display value="MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED" />
      </concept>
      <concept>
        <code value="OMIM:300971" />
        <display value="BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT" />
      </concept>
      <concept>
        <code value="OMIM:300972" />
        <display value="IMMUNODEFICIENCY 47" />
      </concept>
      <concept>
        <code value="OMIM:300977" />
        <display value="SCHOLTE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300978" />
        <display value="TONNE-KALSCHEUER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300979" />
        <display value="Xq25 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300982" />
        <display value="MENTAL RETARDATION, X-LINKED 103" />
      </concept>
      <concept>
        <code value="OMIM:300983" />
        <display value="MENTAL RETARDATION, X-LINKED 104" />
      </concept>
      <concept>
        <code value="OMIM:300984" />
        <display value="MENTAL RETARDATION, X-LINKED 105" />
      </concept>
      <concept>
        <code value="OMIM:300985" />
        <display value="VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300986" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:300988" />
        <display value="IMMUNODEFICIENCY 50" />
      </concept>
      <concept>
        <code value="OMIM:300989" />
        <display value="MEESTER-LOEYS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:300990" />
        <display value="MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS" />
      </concept>
      <concept>
        <code value="OMIM:300991" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:300997" />
        <display value="MENTAL RETARDATION, X-LINKED 106" />
      </concept>
      <concept>
        <code value="OMIM:300998" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35" />
      </concept>
      <concept>
        <code value="OMIM:301000" />
        <display value="WISKOTT-ALDRICH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:301006" />
        <display value="GALLOWAY-MOWAT SYNDROME 2, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:301008" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:301010" />
        <display value="MYOPIA 26, X-LINKED, FEMALE-LIMITED" />
      </concept>
      <concept>
        <code value="OMIM:301013" />
        <display value="MENTAL RETARDATION, X-LINKED 107" />
      </concept>
      <concept>
        <code value="OMIM:301014" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XIX" />
      </concept>
      <concept>
        <code value="OMIM:301015" />
        <display value="HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:301018" />
        <display value="DEAFNESS, X-LINKED 7" />
      </concept>
      <concept>
        <code value="OMIM:301040" />
        <display value="ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:301050" />
        <display value="ALPORT SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:301200" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IE" />
      </concept>
      <concept>
        <code value="OMIM:301201" />
        <display value="AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2" />
      </concept>
      <concept>
        <code value="OMIM:301220" />
        <display value="PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:301310" />
        <display value="ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:301410" />
        <display value="NEURAL TUBE DEFECTS, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:301500" />
        <display value="FABRY DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:301590" />
        <display value="MICROPHTHALMIA, SYNDROMIC 4" />
      </concept>
      <concept>
        <code value="OMIM:301700" />
        <display value="ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:301790" />
        <display value="SPINOCEREBELLAR ATAXIA, X-LINKED 3" />
      </concept>
      <concept>
        <code value="OMIM:301800" />
        <display value="ANUS, IMPERFORATE" />
      </concept>
      <concept>
        <code value="OMIM:301815" />
        <display value="ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:301830" />
        <display value="SPINAL MUSCULAR ATROPHY, X-LINKED 2" />
      </concept>
      <concept>
        <code value="OMIM:301835" />
        <display value="ARTS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:301840" />
        <display value="SPINOCEREBELLAR ATAXIA, X-LINKED 4" />
      </concept>
      <concept>
        <code value="OMIM:301845" />
        <display value="BAZEX SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:301850" />
        <display value="TUBULIN, BETA" />
      </concept>
      <concept>
        <code value="OMIM:301900" />
        <display value="BORJESON-FORSSMAN-LEHMANN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:301940" />
        <display value="BRACHYDACTYLY, MONONEN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:301950" />
        <display value="BRANCHIAL ARCH SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:302000" />
        <display value="BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE" />
      </concept>
      <concept>
        <code value="OMIM:302030" />
        <display value="CALVARIAL HYPEROSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:302045" />
        <display value="CARDIOMYOPATHY, DILATED, 3B" />
      </concept>
      <concept>
        <code value="OMIM:302060" />
        <display value="BARTH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:302200" />
        <display value="CATARACT 40" />
      </concept>
      <concept>
        <code value="OMIM:302350" />
        <display value="NANCE-HORAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:302400" />
        <display value="CENTRAL INCISORS, ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:302500" />
        <display value="SPINOCEREBELLAR ATAXIA, X-LINKED 1" />
      </concept>
      <concept>
        <code value="OMIM:302600" />
        <display value="SPINOCEREBELLAR ATAXIA, X-LINKED 2" />
      </concept>
      <concept>
        <code value="OMIM:302700" />
        <display value="CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE" />
      </concept>
      <concept>
        <code value="OMIM:302800" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1" />
      </concept>
      <concept>
        <code value="OMIM:302801" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:302802" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3" />
      </concept>
      <concept>
        <code value="OMIM:302803" />
        <display value="CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA CUTIS CONGENITA" />
      </concept>
      <concept>
        <code value="OMIM:302900" />
        <display value="CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA, COMBINED" />
      </concept>
      <concept>
        <code value="OMIM:302905" />
        <display value="ABRUZZO-ERICKSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:302950" />
        <display value="CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:302960" />
        <display value="CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:303100" />
        <display value="CHOROIDEREMIA" />
      </concept>
      <concept>
        <code value="OMIM:303110" />
        <display value="CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:303350" />
        <display value="MASA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:303400" />
        <display value="CLEFT PALATE WITH OR WITHOUT ANKYLOGLOSSIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:303600" />
        <display value="COFFIN-LOWRY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:303650" />
        <display value="COLONIC ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:303700" />
        <display value="BLUE CONE MONOCHROMACY" />
      </concept>
      <concept>
        <code value="OMIM:303800" />
        <display value="COLORBLINDNESS, PARTIAL, DEUTAN SERIES" />
      </concept>
      <concept>
        <code value="OMIM:303900" />
        <display value="COLORBLINDNESS, PARTIAL, PROTAN SERIES" />
      </concept>
      <concept>
        <code value="OMIM:304020" />
        <display value="CONE-ROD DYSTROPHY, X-LINKED, 1" />
      </concept>
      <concept>
        <code value="OMIM:304030" />
        <display value="CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN" />
      </concept>
      <concept>
        <code value="OMIM:304050" />
        <display value="AICARDI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:304100" />
        <display value="CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:304110" />
        <display value="CRANIOFRONTONASAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:304120" />
        <display value="OTOPALATODIGITAL SYNDROME, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:304150" />
        <display value="OCCIPITAL HORN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:304200" />
        <display value="CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:304300" />
        <display value="CYANIDE, INABILITY TO SMELL" />
      </concept>
      <concept>
        <code value="OMIM:304340" />
        <display value="PETTIGREW SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:304350" />
        <display value="DEAFNESS-HYPOGONADISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:304400" />
        <display value="DEAFNESS, X-LINKED 2" />
      </concept>
      <concept>
        <code value="OMIM:304500" />
        <display value="DEAFNESS, X-LINKED 1" />
      </concept>
      <concept>
        <code value="OMIM:304700" />
        <display value="MOHR-TRANEBJAERG SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:304730" />
        <display value="DERMOIDS OF CORNEA" />
      </concept>
      <concept>
        <code value="OMIM:304790" />
        <display value="IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:304800" />
        <display value="DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:304900" />
        <display value="DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:304950" />
        <display value="DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:305000" />
        <display value="DYSKERATOSIS CONGENITA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:305100" />
        <display value="ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:305200" />
        <display value="EHLERS-DANLOS SYNDROME, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:305350" />
        <display value="EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:305390" />
        <display value="EXUDATIVE VITREORETINOPATHY 2, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:305400" />
        <display value="AARSKOG-SCOTT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:305435" />
        <display value="FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:305450" />
        <display value="OPITZ-KAVEGGIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:305550" />
        <display value="FINGERPRINT BODY MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:305600" />
        <display value="FOCAL DERMAL HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:305620" />
        <display value="FRONTOMETAPHYSEAL DYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:305690" />
        <display value="GENITOURINARY TRACT ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:305700" />
        <display value="SPERMATOGENIC FAILURE, X-LINKED, 1" />
      </concept>
      <concept>
        <code value="OMIM:305800" />
        <display value="MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:305920" />
        <display value="GLUTAMYL RIBOSE-5-PHOSPHATE STORAGE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:306000" />
        <display value="GLYCOGEN STORAGE DISEASE IXa1" />
      </concept>
      <concept>
        <code value="OMIM:306300" />
        <display value="GRANULOMAS, CONGENITAL CEREBRAL" />
      </concept>
      <concept>
        <code value="OMIM:306400" />
        <display value="GRANULOMATOUS DISEASE, CHRONIC, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:306700" />
        <display value="HEMOPHILIA A" />
      </concept>
      <concept>
        <code value="OMIM:306800" />
        <display value="HEMOPHILIA A WITH VASCULAR ABNORMALITY" />
      </concept>
      <concept>
        <code value="OMIM:306900" />
        <display value="HEMOPHILIA B" />
      </concept>
      <concept>
        <code value="OMIM:306930" />
        <display value="HEMOPOIETIC PROLIFERATION" />
      </concept>
      <concept>
        <code value="OMIM:306950" />
        <display value="HERNIA, ANTERIOR DIAPHRAGMATIC" />
      </concept>
      <concept>
        <code value="OMIM:306955" />
        <display value="HETEROTAXY, VISCERAL, 1, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:306960" />
        <display value="HHHH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:306980" />
        <display value="HIRSCHSPRUNG DISEASE WITH TYPE D BRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:306990" />
        <display value="HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE" />
      </concept>
      <concept>
        <code value="OMIM:306995" />
        <display value="HOMOSEXUALITY 1" />
      </concept>
      <concept>
        <code value="OMIM:307000" />
        <display value="HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS" />
      </concept>
      <concept>
        <code value="OMIM:307010" />
        <display value="HYDROCEPHALUS WITH CEREBELLAR AGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:307030" />
        <display value="GLYCEROL KINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:307150" />
        <display value="HYPERTRICHOSIS, CONGENITAL GENERALIZED" />
      </concept>
      <concept>
        <code value="OMIM:307200" />
        <display value="ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III, WITH AGAMMAGLOBULINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:307500" />
        <display value="HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:307700" />
        <display value="HYPOPARATHYROIDISM, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:307800" />
        <display value="HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:307830" />
        <display value="HYPOURICEMIA, FAMILIAL RENAL, DUE TO TUBULAR HYPERSECRETION" />
      </concept>
      <concept>
        <code value="OMIM:308050" />
        <display value="CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:308100" />
        <display value="ICHTHYOSIS, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:308200" />
        <display value="ICHTHYOSIS AND MALE HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:308205" />
        <display value="IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:308220" />
        <display value="IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACE GLYCOPROTEIN" />
      </concept>
      <concept>
        <code value="OMIM:308230" />
        <display value="IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:308240" />
        <display value="LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1" />
      </concept>
      <concept>
        <code value="OMIM:308250" />
        <display value="IMMUNOGLOBULIN M, LEVEL OF" />
      </concept>
      <concept>
        <code value="OMIM:308280" />
        <display value="IMPACTED TEETH, MULTIPLE" />
      </concept>
      <concept>
        <code value="OMIM:308290" />
        <display value="IMPRINTING GENE RELATED TO RETINOBLASTOMA" />
      </concept>
      <concept>
        <code value="OMIM:308300" />
        <display value="INCONTINENTIA PIGMENTI" />
      </concept>
      <concept>
        <code value="OMIM:308350" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1" />
      </concept>
      <concept>
        <code value="OMIM:308500" />
        <display value="IRIS HYPOPLASIA WITH GLAUCOMA" />
      </concept>
      <concept>
        <code value="OMIM:308600" />
        <display value="JAUNDICE, FAMILIAL OBSTRUCTIVE, OF INFANCY" />
      </concept>
      <concept>
        <code value="OMIM:308700" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:308750" />
        <display value="KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA" />
      </concept>
      <concept>
        <code value="OMIM:308800" />
        <display value="KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:308830" />
        <display value="KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:308850" />
        <display value="LARYNGEAL ABDUCTOR PARALYSIS" />
      </concept>
      <concept>
        <code value="OMIM:308905" />
        <display value="LEBER OPTIC ATROPHY, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:308940" />
        <display value="LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:308950" />
        <display value="LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT" />
      </concept>
      <concept>
        <code value="OMIM:308960" />
        <display value="LEUKEMIA, ACUTE, ?X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:308990" />
        <display value="PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS" />
      </concept>
      <concept>
        <code value="OMIM:309000" />
        <display value="LOWE OCULOCEREBRORENAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:309050" />
        <display value="LUTHERAN SUPPRESSOR, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:309100" />
        <display value="MACULAR DYSTROPHY, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:309120" />
        <display value="SPERMATOGENIC FAILURE, X-LINKED, 2" />
      </concept>
      <concept>
        <code value="OMIM:309200" />
        <display value="MAJOR AFFECTIVE DISORDER 2" />
      </concept>
      <concept>
        <code value="OMIM:309300" />
        <display value="MEGALOCORNEA" />
      </concept>
      <concept>
        <code value="OMIM:309350" />
        <display value="MELNICK-NEEDLES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:309400" />
        <display value="MENKES DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:309480" />
        <display value="MENTAL RETARDATION AND PSORIASIS" />
      </concept>
      <concept>
        <code value="OMIM:309500" />
        <display value="RENPENNING SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:309510" />
        <display value="PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:309520" />
        <display value="LUJAN-FRYNS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:309530" />
        <display value="MENTAL RETARDATION, X-LINKED 1" />
      </concept>
      <concept>
        <code value="OMIM:309541" />
        <display value="METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE" />
      </concept>
      <concept>
        <code value="OMIM:309545" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC 12" />
      </concept>
      <concept>
        <code value="OMIM:309548" />
        <display value="MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE" />
      </concept>
      <concept>
        <code value="OMIM:309549" />
        <display value="MENTAL RETARDATION, X-LINKED 9" />
      </concept>
      <concept>
        <code value="OMIM:309555" />
        <display value="MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:309560" />
        <display value="MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:309580" />
        <display value="MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1" />
      </concept>
      <concept>
        <code value="OMIM:309583" />
        <display value="MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE" />
      </concept>
      <concept>
        <code value="OMIM:309585" />
        <display value="WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:309610" />
        <display value="PRIETO X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:309620" />
        <display value="MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY" />
      </concept>
      <concept>
        <code value="OMIM:309630" />
        <display value="METACARPAL 4-5 FUSION" />
      </concept>
      <concept>
        <code value="OMIM:309640" />
        <display value="MENTAL RETARDATION WITH SPASTIC PARAPLEGIA" />
      </concept>
      <concept>
        <code value="OMIM:309800" />
        <display value="MICROPHTHALMIA, SYNDROMIC 1" />
      </concept>
      <concept>
        <code value="OMIM:309801" />
        <display value="LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 1" />
      </concept>
      <concept>
        <code value="OMIM:309840" />
        <display value="MODIFIER, X-LINKED, FOR NEUROFUNCTIONAL DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:309900" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:309930" />
        <display value="MUSCULAR DYSTROPHY, CARDIAC TYPE" />
      </concept>
      <concept>
        <code value="OMIM:309950" />
        <display value="MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:310000" />
        <display value="MUSCULAR DYSTROPHY, MABRY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:310095" />
        <display value="MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL" />
      </concept>
      <concept>
        <code value="OMIM:310200" />
        <display value="MUSCULAR DYSTROPHY, DUCHENNE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:310300" />
        <display value="EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:310350" />
        <display value="MYELOLYMPHATIC INSUFFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:310370" />
        <display value="MYOCLONIC EPILEPSY, PROGRESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:310400" />
        <display value="MYOPATHY, CENTRONUCLEAR, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:310440" />
        <display value="MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY" />
      </concept>
      <concept>
        <code value="OMIM:310460" />
        <display value="MYOPIA 1, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:310465" />
        <display value="N SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:310468" />
        <display value="NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE" />
      </concept>
      <concept>
        <code value="OMIM:310470" />
        <display value="NEUROPATHY, HEREDITARY SENSORY, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:310490" />
        <display value="COWCHOCK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:310500" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A" />
      </concept>
      <concept>
        <code value="OMIM:310600" />
        <display value="NORRIE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:310650" />
        <display value="NUCLEAR RIBONUCLEIC ACID" />
      </concept>
      <concept>
        <code value="OMIM:310700" />
        <display value="NYSTAGMUS 1, CONGENITAL, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:310800" />
        <display value="NYSTAGMUS, MYOCLONIC" />
      </concept>
      <concept>
        <code value="OMIM:310900" />
        <display value="OCCIPITAL HAIR, WHITE LOCK OF" />
      </concept>
      <concept>
        <code value="OMIM:310980" />
        <display value="OMPHALOCELE, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:311000" />
        <display value="OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA" />
      </concept>
      <concept>
        <code value="OMIM:311050" />
        <display value="OPTIC ATROPHY 2" />
      </concept>
      <concept>
        <code value="OMIM:311070" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5" />
      </concept>
      <concept>
        <code value="OMIM:311100" />
        <display value="OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:311200" />
        <display value="OROFACIODIGITAL SYNDROME I" />
      </concept>
      <concept>
        <code value="OMIM:311250" />
        <display value="ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:311300" />
        <display value="OTOPALATODIGITAL SYNDROME, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:311350" />
        <display value="OUABAIN RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:311360" />
        <display value="PREMATURE OVARIAN FAILURE 1" />
      </concept>
      <concept>
        <code value="OMIM:311400" />
        <display value="PAINE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:311450" />
        <display value="PALLISTER W SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:311510" />
        <display value="WAISMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:311895" />
        <display value="PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:311900" />
        <display value="TARP SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:312000" />
        <display value="PANHYPOPITUITARISM, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:312060" />
        <display value="PROPERDIN DEFICIENCY, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:312080" />
        <display value="PELIZAEUS-MERZBACHER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:312150" />
        <display value="MULTIPLE PTERYGIUM SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:312170" />
        <display value="PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:312190" />
        <display value="RADIAL APLASIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:312200" />
        <display value="RADIAL LOOP, PLAIN, ON RIGHT INDEX FINGER" />
      </concept>
      <concept>
        <code value="OMIM:312210" />
        <display value="RADIATION SENSITIVITY OF NATURAL KILLER ACTIVITY" />
      </concept>
      <concept>
        <code value="OMIM:312300" />
        <display value="ANDROGEN INSENSITIVITY, PARTIAL" />
      </concept>
      <concept>
        <code value="OMIM:312500" />
        <display value="RETICULOENDOTHELIOSIS, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:312550" />
        <display value="RETINAL DYSPLASIA, PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:312600" />
        <display value="RETINITIS PIGMENTOSA 2" />
      </concept>
      <concept>
        <code value="OMIM:312612" />
        <display value="RETINITIS PIGMENTOSA 6" />
      </concept>
      <concept>
        <code value="OMIM:312700" />
        <display value="RETINOSCHISIS 1, X-LINKED, JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:312750" />
        <display value="RETT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:312780" />
        <display value="RUSSELL-SILVER SYNDROME, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:312830" />
        <display value="SCARF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:312840" />
        <display value="SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:312863" />
        <display value="COMBINED IMMUNODEFICIENCY, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:312870" />
        <display value="SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:312910" />
        <display value="SPASTIC PARAPARESIS AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:312920" />
        <display value="SPASTIC PARAPLEGIA 2, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:313000" />
        <display value="SPATIAL VISUALIZATION, APTITUDE FOR" />
      </concept>
      <concept>
        <code value="OMIM:313200" />
        <display value="SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1" />
      </concept>
      <concept>
        <code value="OMIM:313350" />
        <display value="SPLIT-HAND/FOOT MALFORMATION 2" />
      </concept>
      <concept>
        <code value="OMIM:313400" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:313420" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:313480" />
        <display value="TaqI POLYMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:313490" />
        <display value="TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS" />
      </concept>
      <concept>
        <code value="OMIM:313500" />
        <display value="TOOTH AGENESIS, SELECTIVE, X-LINKED, 1" />
      </concept>
      <concept>
        <code value="OMIM:313850" />
        <display value="THORACOABDOMINAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:313900" />
        <display value="THROMBOCYTOPENIA 1" />
      </concept>
      <concept>
        <code value="OMIM:314000" />
        <display value="THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:314050" />
        <display value="THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:314100" />
        <display value="THUMBS, CONGENITAL CLASPED" />
      </concept>
      <concept>
        <code value="OMIM:314240" />
        <display value="TOOTH SIZE" />
      </concept>
      <concept>
        <code value="OMIM:314250" />
        <display value="DYSTONIA 3, TORSION, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:314300" />
        <display value="TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:314320" />
        <display value="TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:314360" />
        <display value="ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET" />
      </concept>
      <concept>
        <code value="OMIM:314380" />
        <display value="UNIQUE GREEN PHENOMENON" />
      </concept>
      <concept>
        <code value="OMIM:314390" />
        <display value="VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS" />
      </concept>
      <concept>
        <code value="OMIM:314400" />
        <display value="CARDIAC VALVULAR DYSPLASIA, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:314500" />
        <display value="VAN DEN BOSCH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:314550" />
        <display value="VESICOURETERAL REFLUX, X-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:314560" />
        <display value="VON WILLEBRAND DISEASE, X-LINKED FORM" />
      </concept>
      <concept>
        <code value="OMIM:314570" />
        <display value="WIDOW'S PEAK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:314580" />
        <display value="WIEACKER-WOLFF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:314600" />
        <display value="WILDERVANCK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:314700" />
        <display value="BLOOD GROUP, XG SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:314705" />
        <display value="XG REGULATOR" />
      </concept>
      <concept>
        <code value="OMIM:314800" />
        <display value="XH ANTIGEN" />
      </concept>
      <concept>
        <code value="OMIM:314900" />
        <display value="XM SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:400004" />
        <display value="RETINITIS PIGMENTOSA, Y-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:400021" />
        <display value="LYMPHOMA, HODGKIN, Y-LINKED PSEUDOAUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:400042" />
        <display value="SPERMATOGENIC FAILURE, Y-LINKED, 1" />
      </concept>
      <concept>
        <code value="OMIM:400043" />
        <display value="DEAFNESS, Y-LINKED 1" />
      </concept>
      <concept>
        <code value="OMIM:400044" />
        <display value="46,XY SEX REVERSAL 1" />
      </concept>
      <concept>
        <code value="OMIM:400045" />
        <display value="46,XX SEX REVERSAL 1" />
      </concept>
      <concept>
        <code value="OMIM:415000" />
        <display value="SPERMATOGENIC FAILURE, Y-LINKED, 2" />
      </concept>
      <concept>
        <code value="OMIM:424500" />
        <display value="GONADOBLASTOMA" />
      </concept>
      <concept>
        <code value="OMIM:425500" />
        <display value="HAIRY EARS, Y-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:475000" />
        <display value="GROWTH CONTROL, Y-CHROMOSOME INFLUENCED" />
      </concept>
      <concept>
        <code value="OMIM:489000" />
        <display value="UBIQUITIN-ACTIVATING ENZYME, Y-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:500000" />
        <display value="CARDIOMYOPATHY, INFANTILE HISTIOCYTOID" />
      </concept>
      <concept>
        <code value="OMIM:500001" />
        <display value="LEBER OPTIC ATROPHY AND DYSTONIA" />
      </concept>
      <concept>
        <code value="OMIM:500002" />
        <display value="MITOCHONDRIAL MYOPATHY WITH DIABETES" />
      </concept>
      <concept>
        <code value="OMIM:500003" />
        <display value="STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL" />
      </concept>
      <concept>
        <code value="OMIM:500004" />
        <display value="RETINITIS PIGMENTOSA-DEAFNESS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:500005" />
        <display value="HYPOMAGNESEMIA, HYPERTENSION, AND HYPERCHOLESTEROLEMIA, MITOCHONDRIAL" />
      </concept>
      <concept>
        <code value="OMIM:500006" />
        <display value="CARDIOMYOPATHY, INFANTILE HYPERTROPHIC" />
      </concept>
      <concept>
        <code value="OMIM:500007" />
        <display value="CYCLIC VOMITING SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:500008" />
        <display value="DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL" />
      </concept>
      <concept>
        <code value="OMIM:500009" />
        <display value="MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT" />
      </concept>
      <concept>
        <code value="OMIM:500010" />
        <display value="ATAXIA AND POLYNEUROPATHY, ADULT-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:500011" />
        <display value="MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3" />
      </concept>
      <concept>
        <code value="OMIM:502000" />
        <display value="AGING" />
      </concept>
      <concept>
        <code value="OMIM:502500" />
        <display value="ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL" />
      </concept>
      <concept>
        <code value="OMIM:515000" />
        <display value="CHLORAMPHENICOL TOXICITY" />
      </concept>
      <concept>
        <code value="OMIM:516060" />
        <display value="ATP SYNTHASE 6" />
      </concept>
      <concept>
        <code value="OMIM:516070" />
        <display value="ATP SYNTHASE 8" />
      </concept>
      <concept>
        <code value="OMIM:520000" />
        <display value="DIABETES AND DEAFNESS, MATERNALLY INHERITED" />
      </concept>
      <concept>
        <code value="OMIM:520100" />
        <display value="DIARRHEA, CHRONIC, WITH VILLOUS ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:530000" />
        <display value="KEARNS-SAYRE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:535000" />
        <display value="LEBER OPTIC ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:540000" />
        <display value="MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES" />
      </concept>
      <concept>
        <code value="OMIM:545000" />
        <display value="MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS" />
      </concept>
      <concept>
        <code value="OMIM:550500" />
        <display value="MYOGLOBINURIA, RECURRENT" />
      </concept>
      <concept>
        <code value="OMIM:551000" />
        <display value="MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:551200" />
        <display value="NEPHROPATHY, CHRONIC TUBULOINTERSTITIAL" />
      </concept>
      <concept>
        <code value="OMIM:551500" />
        <display value="NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA" />
      </concept>
      <concept>
        <code value="OMIM:553000" />
        <display value="ONCOCYTOMA" />
      </concept>
      <concept>
        <code value="OMIM:556500" />
        <display value="PARKINSON DISEASE, MITOCHONDRIAL" />
      </concept>
      <concept>
        <code value="OMIM:557000" />
        <display value="PEARSON MARROW-PANCREAS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:560000" />
        <display value="RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:580000" />
        <display value="DEAFNESS, AMINOGLYCOSIDE-INDUCED" />
      </concept>
      <concept>
        <code value="OMIM:598500" />
        <display value="WOLFRAM SYNDROME, MITOCHONDRIAL FORM" />
      </concept>
      <concept>
        <code value="OMIM:600000" />
        <display value="SPONDYLOCAMPTODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:600001" />
        <display value="HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:600002" />
        <display value="EIKEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600046" />
        <display value="ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 1" />
      </concept>
      <concept>
        <code value="OMIM:600057" />
        <display value="EXSTROPHY OF BLADDER" />
      </concept>
      <concept>
        <code value="OMIM:600059" />
        <display value="RETINITIS PIGMENTOSA 13" />
      </concept>
      <concept>
        <code value="OMIM:600060" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:600072" />
        <display value="FATAL FAMILIAL INSOMNIA" />
      </concept>
      <concept>
        <code value="OMIM:600080" />
        <display value="MYELOCYTIC LEUKEMIA-LIKE SYNDROME, FAMILIAL, CHRONIC" />
      </concept>
      <concept>
        <code value="OMIM:600081" />
        <display value="VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B" />
      </concept>
      <concept>
        <code value="OMIM:600082" />
        <display value="PROSTATIC HYPERPLASIA, BENIGN" />
      </concept>
      <concept>
        <code value="OMIM:600084" />
        <display value="MACROCYTOSIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:600089" />
        <display value="PANCREATIC BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS" />
      </concept>
      <concept>
        <code value="OMIM:600092" />
        <display value="CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600093" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES" />
      </concept>
      <concept>
        <code value="OMIM:600096" />
        <display value="PUERTO RICAN INFANT HYPOTONIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600101" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 2A" />
      </concept>
      <concept>
        <code value="OMIM:600105" />
        <display value="RETINITIS PIGMENTOSA 12" />
      </concept>
      <concept>
        <code value="OMIM:600110" />
        <display value="STARGARDT DISEASE 3" />
      </concept>
      <concept>
        <code value="OMIM:600116" />
        <display value="PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:600117" />
        <display value="DYSPHASIA, FAMILIAL DEVELOPMENTAL" />
      </concept>
      <concept>
        <code value="OMIM:600118" />
        <display value="WARBURG MICRO SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:600121" />
        <display value="RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:600122" />
        <display value="MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE" />
      </concept>
      <concept>
        <code value="OMIM:600123" />
        <display value="ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL AND RADIAL DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:600131" />
        <display value="EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:600132" />
        <display value="RETINITIS PIGMENTOSA 14" />
      </concept>
      <concept>
        <code value="OMIM:600138" />
        <display value="RETINITIS PIGMENTOSA 11" />
      </concept>
      <concept>
        <code value="OMIM:600142" />
        <display value="CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:600143" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 8" />
      </concept>
      <concept>
        <code value="OMIM:600145" />
        <display value="SACRAL DEFECT WITH ANTERIOR MENINGOCELE" />
      </concept>
      <concept>
        <code value="OMIM:600148" />
        <display value="GLYCEROL KINASE 2" />
      </concept>
      <concept>
        <code value="OMIM:600149" />
        <display value="GLYCEROL KINASE 3 PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:600151" />
        <display value="BARDET-BIEDL SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:600155" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:600156" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:600159" />
        <display value="PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:600165" />
        <display value="NANOPHTHALMOS 1" />
      </concept>
      <concept>
        <code value="OMIM:600166" />
        <display value="HYPERPARATHYROIDISM, PRIMARY, CAUSED BY WATER CLEAR CELL HYPERPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:600171" />
        <display value="GONADAL AGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:600175" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII" />
      </concept>
      <concept>
        <code value="OMIM:600176" />
        <display value="PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:600193" />
        <display value="WAARDENBURG SYNDROME, TYPE 2B" />
      </concept>
      <concept>
        <code value="OMIM:600195" />
        <display value="VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL" />
      </concept>
      <concept>
        <code value="OMIM:600202" />
        <display value="DYSLEXIA, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:600204" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, 2" />
      </concept>
      <concept>
        <code value="OMIM:600209" />
        <display value="EXOSTOSES, MULTIPLE, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:600223" />
        <display value="SPINOCEREBELLAR ATAXIA 4" />
      </concept>
      <concept>
        <code value="OMIM:600224" />
        <display value="SPINOCEREBELLAR ATAXIA 5" />
      </concept>
      <concept>
        <code value="OMIM:600231" />
        <display value="PALMOPLANTAR KERATODERMA, BOTHNIAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:600251" />
        <display value="FACIAL CLEFTING, OBLIQUE, 1" />
      </concept>
      <concept>
        <code value="OMIM:600252" />
        <display value="LOWRY-MACLEAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600257" />
        <display value="CHROMOSOME 8q12.1-q21.2 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600263" />
        <display value="HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:600268" />
        <display value="OCULOECTODERMAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600269" />
        <display value="SHORT TARSUS WITH ABSENCE OF LOWER EYELASHES" />
      </concept>
      <concept>
        <code value="OMIM:600273" />
        <display value="POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS" />
      </concept>
      <concept>
        <code value="OMIM:600274" />
        <display value="FRONTOTEMPORAL DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:600302" />
        <display value="FRYNS MACROCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:600309" />
        <display value="ATRIOVENTRICULAR SEPTAL DEFECT 3" />
      </concept>
      <concept>
        <code value="OMIM:600316" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:600318" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 3" />
      </concept>
      <concept>
        <code value="OMIM:600319" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 4" />
      </concept>
      <concept>
        <code value="OMIM:600320" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 5" />
      </concept>
      <concept>
        <code value="OMIM:600321" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 7" />
      </concept>
      <concept>
        <code value="OMIM:600325" />
        <display value="AMINOPTERIN SYNDROME SINE AMINOPTERIN" />
      </concept>
      <concept>
        <code value="OMIM:600329" />
        <display value="OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:600331" />
        <display value="PARC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600332" />
        <display value="RIPPLING MUSCLE DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:600333" />
        <display value="MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA" />
      </concept>
      <concept>
        <code value="OMIM:600334" />
        <display value="TIBIAL MUSCULAR DYSTROPHY, TARDIVE" />
      </concept>
      <concept>
        <code value="OMIM:600335" />
        <display value="SUCCINIC ACIDEMIA" />
      </concept>
      <concept>
        <code value="OMIM:600343" />
        <display value="PAROTID SALIVARY GLANDS, POLYCYSTIC DYSGENETIC DISEASE OF" />
      </concept>
      <concept>
        <code value="OMIM:600348" />
        <display value="BAND HETEROTOPIA" />
      </concept>
      <concept>
        <code value="OMIM:600351" />
        <display value="ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:600356" />
        <display value="PACHYDERMODACTYLY, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:600360" />
        <display value="APLASIA CUTIS CONGENITA OF LIMBS, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:600361" />
        <display value="HEREDITARY MOTOR AND SENSORY NEUROPATHY V" />
      </concept>
      <concept>
        <code value="OMIM:600363" />
        <display value="SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:600373" />
        <display value="CODAS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600376" />
        <display value="TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:600383" />
        <display value="MESOMELIA-SYNOSTOSES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600384" />
        <display value="APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSAL IV" />
      </concept>
      <concept>
        <code value="OMIM:600399" />
        <display value="PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS" />
      </concept>
      <concept>
        <code value="OMIM:600416" />
        <display value="MUSCULAR DYSTROPHY, SCAPULOHUMERAL" />
      </concept>
      <concept>
        <code value="OMIM:600419" />
        <display value="ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS" />
      </concept>
      <concept>
        <code value="OMIM:600430" />
        <display value="CHROMOSOME 2q37 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600457" />
        <display value="HYPERTRICHOSIS, ANTERIOR CERVICAL" />
      </concept>
      <concept>
        <code value="OMIM:600458" />
        <display value="ADENOMYOSIS" />
      </concept>
      <concept>
        <code value="OMIM:600459" />
        <display value="ARTERIAL DISSECTION WITH LENTIGINOSIS" />
      </concept>
      <concept>
        <code value="OMIM:600460" />
        <display value="CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:600461" />
        <display value="HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:600462" />
        <display value="MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1" />
      </concept>
      <concept>
        <code value="OMIM:600467" />
        <display value="MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:600496" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:600501" />
        <display value="ABCD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600510" />
        <display value="GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600511" />
        <display value="SCHIZOPHRENIA 3" />
      </concept>
      <concept>
        <code value="OMIM:600512" />
        <display value="EPILEPSY, FAMILIAL TEMPORAL LOBE, 1" />
      </concept>
      <concept>
        <code value="OMIM:600513" />
        <display value="EPILEPSY, NOCTURNAL FRONTAL LOBE, 1" />
      </concept>
      <concept>
        <code value="OMIM:600522" />
        <display value="PHOSPHOLIPASE A2, GROUP IVA" />
      </concept>
      <concept>
        <code value="OMIM:600546" />
        <display value="INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:600559" />
        <display value="HYDROCEPHALUS, ENDOCARDIAL FIBROELASTOSIS, AND CATARACTS" />
      </concept>
      <concept>
        <code value="OMIM:600561" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY" />
      </concept>
      <concept>
        <code value="OMIM:600593" />
        <display value="CRANIOSYNOSTOSIS, ADELAIDE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:600598" />
        <display value="SETTING-SUN PHENOMENON, FAMILIAL BENIGN" />
      </concept>
      <concept>
        <code value="OMIM:600624" />
        <display value="CONE-ROD DYSTROPHY 1" />
      </concept>
      <concept>
        <code value="OMIM:600625" />
        <display value="OROFACIAL CLEFT 11" />
      </concept>
      <concept>
        <code value="OMIM:600627" />
        <display value="HYPERTRYPTOPHANEMIA" />
      </concept>
      <concept>
        <code value="OMIM:600628" />
        <display value="LOOSE ANAGEN HAIR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600630" />
        <display value="UV-SENSITIVE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:600631" />
        <display value="ENURESIS, NOCTURNAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:600634" />
        <display value="PITUITARY ADENOMA, PROLACTIN-SECRETING" />
      </concept>
      <concept>
        <code value="OMIM:600638" />
        <display value="FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT" />
      </concept>
      <concept>
        <code value="OMIM:600643" />
        <display value="CAROLI DISEASE, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:600649" />
        <display value="CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:600651" />
        <display value="FRAGILE SITE 11B" />
      </concept>
      <concept>
        <code value="OMIM:600652" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 4A" />
      </concept>
      <concept>
        <code value="OMIM:600666" />
        <display value="POLYCYSTIC KIDNEY DISEASE 3 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:600668" />
        <display value="CHONDROCALCINOSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:600669" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED" />
      </concept>
      <concept>
        <code value="OMIM:600670" />
        <display value="VARICELLA, SEVERE RECURRENT" />
      </concept>
      <concept>
        <code value="OMIM:600674" />
        <display value="MICROTIA-ANOTIA" />
      </concept>
      <concept>
        <code value="OMIM:600679" />
        <display value="DERMOID CYSTS, FAMILIAL FRONTONASAL" />
      </concept>
      <concept>
        <code value="OMIM:600705" />
        <display value="SATOYOSHI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600706" />
        <display value="PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA" />
      </concept>
      <concept>
        <code value="OMIM:600721" />
        <display value="D-2-HYDROXYGLUTARIC ACIDURIA 1" />
      </concept>
      <concept>
        <code value="OMIM:600736" />
        <display value="VELOFACIOSKELETAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600740" />
        <display value="HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:600757" />
        <display value="OROFACIAL CLEFT 3" />
      </concept>
      <concept>
        <code value="OMIM:600771" />
        <display value="DWARFISM, FAMILIAL, WITH MUSCLE SPASMS" />
      </concept>
      <concept>
        <code value="OMIM:600775" />
        <display value="CRANIOSYNOSTOSIS 4" />
      </concept>
      <concept>
        <code value="OMIM:600776" />
        <display value="FRYNS MICROPHTHALMIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600785" />
        <display value="VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR" />
      </concept>
      <concept>
        <code value="OMIM:600790" />
        <display value="CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL" />
      </concept>
      <concept>
        <code value="OMIM:600791" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT" />
      </concept>
      <concept>
        <code value="OMIM:600792" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 5" />
      </concept>
      <concept>
        <code value="OMIM:600794" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA" />
      </concept>
      <concept>
        <code value="OMIM:600795" />
        <display value="FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED" />
      </concept>
      <concept>
        <code value="OMIM:600801" />
        <display value="ISOPROTERENOL-MEDIATED VASODILATATION" />
      </concept>
      <concept>
        <code value="OMIM:600802" />
        <display value="SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE" />
      </concept>
      <concept>
        <code value="OMIM:600803" />
        <display value="GALLBLADDER DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:600807" />
        <display value="ASTHMA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:600808" />
        <display value="ENURESIS, NOCTURNAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:600841" />
        <display value="EUKARYOTIC TRANSLATION ELONGATION FACTOR 1 ALPHA-1-LIKE 14" />
      </concept>
      <concept>
        <code value="OMIM:600850" />
        <display value="SCHIZOPHRENIA 4" />
      </concept>
      <concept>
        <code value="OMIM:600851" />
        <display value="MITOCHONDRIAL IMPORT-STIMULATING FACTOR" />
      </concept>
      <concept>
        <code value="OMIM:600852" />
        <display value="RETINITIS PIGMENTOSA 17" />
      </concept>
      <concept>
        <code value="OMIM:600858" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6" />
      </concept>
      <concept>
        <code value="OMIM:600880" />
        <display value="BUDD-CHIARI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600881" />
        <display value="CATARACT 10, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:600882" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B" />
      </concept>
      <concept>
        <code value="OMIM:600883" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 8" />
      </concept>
      <concept>
        <code value="OMIM:600884" />
        <display value="CARDIOMYOPATHY, DILATED, 1B" />
      </concept>
      <concept>
        <code value="OMIM:600886" />
        <display value="HYPERFERRITINEMIA WITH OR WITHOUT CATARACT" />
      </concept>
      <concept>
        <code value="OMIM:600901" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP E" />
      </concept>
      <concept>
        <code value="OMIM:600903" />
        <display value="WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM" />
      </concept>
      <concept>
        <code value="OMIM:600906" />
        <display value="ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:600907" />
        <display value="ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS" />
      </concept>
      <concept>
        <code value="OMIM:600908" />
        <display value="KENNERKNECHT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600919" />
        <display value="CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:600920" />
        <display value="VAN DEN ENDE-GUPTA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:600931" />
        <display value="PROTOCADHERIN 3" />
      </concept>
      <concept>
        <code value="OMIM:600952" />
        <display value="TRANSSEXUALITY" />
      </concept>
      <concept>
        <code value="OMIM:600955" />
        <display value="PROPROTEIN CONVERTASE 1/3 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:600962" />
        <display value="PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC" />
      </concept>
      <concept>
        <code value="OMIM:600965" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 6" />
      </concept>
      <concept>
        <code value="OMIM:600969" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, 3" />
      </concept>
      <concept>
        <code value="OMIM:600971" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 6" />
      </concept>
      <concept>
        <code value="OMIM:600972" />
        <display value="ACHONDROGENESIS, TYPE IB" />
      </concept>
      <concept>
        <code value="OMIM:600974" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 7" />
      </concept>
      <concept>
        <code value="OMIM:600975" />
        <display value="GLAUCOMA 3, PRIMARY INFANTILE, B" />
      </concept>
      <concept>
        <code value="OMIM:600977" />
        <display value="CONE-ROD DYSTROPHY 5" />
      </concept>
      <concept>
        <code value="OMIM:600987" />
        <display value="CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:600989" />
        <display value="INFUNDIBULOPELVIC DYSGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:600991" />
        <display value="HYDROCEPHALUS, SPRENGEL ANOMALY, AND COSTOVERTEBRAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:600994" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 5" />
      </concept>
      <concept>
        <code value="OMIM:600995" />
        <display value="NEPHROTIC SYNDROME, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:600996" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:601001" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1" />
      </concept>
      <concept>
        <code value="OMIM:601003" />
        <display value="BRODY MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:601004" />
        <display value="PORTAL VEIN, CAVERNOUS TRANSFORMATION OF" />
      </concept>
      <concept>
        <code value="OMIM:601005" />
        <display value="TIMOTHY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601016" />
        <display value="MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM" />
      </concept>
      <concept>
        <code value="OMIM:601027" />
        <display value="TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:601039" />
        <display value="ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN" />
      </concept>
      <concept>
        <code value="OMIM:601042" />
        <display value="DYSTONIA 9" />
      </concept>
      <concept>
        <code value="OMIM:601067" />
        <display value="USHER SYNDROME, TYPE ID" />
      </concept>
      <concept>
        <code value="OMIM:601068" />
        <display value="EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:601071" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 9" />
      </concept>
      <concept>
        <code value="OMIM:601072" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 8" />
      </concept>
      <concept>
        <code value="OMIM:601075" />
        <display value="APLASIA CUTIS CONGENITA, HIGH MYOPIA, AND CONE-ROD DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:601076" />
        <display value="MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACIC SOMITE ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:601083" />
        <display value="CD4/CD8 T-CELL RATIO" />
      </concept>
      <concept>
        <code value="OMIM:601086" />
        <display value="LATERALITY DEFECTS, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:601088" />
        <display value="AYME-GRIPP SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601095" />
        <display value="HARROD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601096" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC" />
      </concept>
      <concept>
        <code value="OMIM:601098" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C" />
      </concept>
      <concept>
        <code value="OMIM:601101" />
        <display value="TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:601104" />
        <display value="SUPRANUCLEAR PALSY, PROGRESSIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:601110" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id" />
      </concept>
      <concept>
        <code value="OMIM:601127" />
        <display value="FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:601136" />
        <display value="TRANSSUPPRESSOR OF EXPRESSION 2" />
      </concept>
      <concept>
        <code value="OMIM:601138" />
        <display value="GUANYLATE CYCLASE 2E, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:601144" />
        <display value="BRUGADA SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:601152" />
        <display value="NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA" />
      </concept>
      <concept>
        <code value="OMIM:601154" />
        <display value="CARDIOMYOPATHY, DILATED, 1E" />
      </concept>
      <concept>
        <code value="OMIM:601160" />
        <display value="LISSENCEPHALY TYPE III AND BONE DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:601161" />
        <display value="TRISOMY 18-LIKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601162" />
        <display value="SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:601163" />
        <display value="DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL" />
      </concept>
      <concept>
        <code value="OMIM:601165" />
        <display value="CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION, AND LETHAL CONGENITAL HEART DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:601170" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS" />
      </concept>
      <concept>
        <code value="OMIM:601186" />
        <display value="MICROPHTHALMIA, SYNDROMIC 9" />
      </concept>
      <concept>
        <code value="OMIM:601187" />
        <display value="GURRIERI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601188" />
        <display value="SUPPRESSION OF TUMORIGENICITY 12" />
      </concept>
      <concept>
        <code value="OMIM:601195" />
        <display value="IRON OVERLOAD IN AFRICA" />
      </concept>
      <concept>
        <code value="OMIM:601198" />
        <display value="HYPOCALCEMIA, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:601200" />
        <display value="PLEUROPULMONARY BLASTOMA" />
      </concept>
      <concept>
        <code value="OMIM:601202" />
        <display value="CATARACT 24" />
      </concept>
      <concept>
        <code value="OMIM:601208" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 11" />
      </concept>
      <concept>
        <code value="OMIM:601214" />
        <display value="NAXOS DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:601216" />
        <display value="DENTAL ANOMALIES AND SHORT STATURE" />
      </concept>
      <concept>
        <code value="OMIM:601217" />
        <display value="ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPIC HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:601220" />
        <display value="OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601221" />
        <display value="TISSUE-SPECIFIC EXTINGUISHER 3" />
      </concept>
      <concept>
        <code value="OMIM:601223" />
        <display value="NEURONAL INTESTINAL DYSPLASIA, TYPE B" />
      </concept>
      <concept>
        <code value="OMIM:601224" />
        <display value="POTOCKI-SHAFFER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601228" />
        <display value="POLYPOSIS SYNDROME, HEREDITARY MIXED, 1" />
      </concept>
      <concept>
        <code value="OMIM:601230" />
        <display value="DERMATITIS HERPETIFORMIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:601238" />
        <display value="CEREBELLAR ATAXIA, CAYMAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601277" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A" />
      </concept>
      <concept>
        <code value="OMIM:601283" />
        <display value="DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1" />
      </concept>
      <concept>
        <code value="OMIM:601287" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 6" />
      </concept>
      <concept>
        <code value="OMIM:601308" />
        <display value="MYELOID TUMOR SUPPRESSOR" />
      </concept>
      <concept>
        <code value="OMIM:601315" />
        <display value="EPITHELIAL BASOLATERAL CHLORIDE CONDUCTANCE REGULATOR, RABBIT, HOMOLOG OF" />
      </concept>
      <concept>
        <code value="OMIM:601316" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 10" />
      </concept>
      <concept>
        <code value="OMIM:601317" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 11" />
      </concept>
      <concept>
        <code value="OMIM:601318" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 13" />
      </concept>
      <concept>
        <code value="OMIM:601319" />
        <display value="ODONTOMICRONYCHIAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:601321" />
        <display value="NEUROFIBROMATOSIS-NOONAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601322" />
        <display value="PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:601331" />
        <display value="RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:601338" />
        <display value="CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS" />
      </concept>
      <concept>
        <code value="OMIM:601341" />
        <display value="ATROPHIA MACULOSA VARIOLIFORMIS CUTIS, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:601344" />
        <display value="SPINAL DYSPLASIA, ANHALT TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601345" />
        <display value="ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601346" />
        <display value="MARTINEZ-FRIAS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601347" />
        <display value="MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE, AND PSYCHOMOTOR DELAY" />
      </concept>
      <concept>
        <code value="OMIM:601348" />
        <display value="ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA" />
      </concept>
      <concept>
        <code value="OMIM:601349" />
        <display value="MICROPHTHALMIA, SYNDROMIC 8" />
      </concept>
      <concept>
        <code value="OMIM:601350" />
        <display value="SHORT STATURE SYNDROME, BRUSSELS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601351" />
        <display value="GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION" />
      </concept>
      <concept>
        <code value="OMIM:601352" />
        <display value="MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE" />
      </concept>
      <concept>
        <code value="OMIM:601353" />
        <display value="BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:601355" />
        <display value="MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS, AND HYPOSEGMENTED LUNGS" />
      </concept>
      <concept>
        <code value="OMIM:601356" />
        <display value="LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601357" />
        <display value="BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:601358" />
        <display value="NICOLAIDES-BARAITSER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601360" />
        <display value="AMELIA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:601362" />
        <display value="DIGEORGE SYNDROME/VELOCARDIOFACIAL SYNDROME COMPLEX 2" />
      </concept>
      <concept>
        <code value="OMIM:601363" />
        <display value="WILMS TUMOR 4" />
      </concept>
      <concept>
        <code value="OMIM:601367" />
        <display value="STROKE, ISCHEMIC" />
      </concept>
      <concept>
        <code value="OMIM:601369" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 9" />
      </concept>
      <concept>
        <code value="OMIM:601370" />
        <display value="HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:601371" />
        <display value="CATARACT, AGE-RELATED NUCLEAR" />
      </concept>
      <concept>
        <code value="OMIM:601372" />
        <display value="CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT" />
      </concept>
      <concept>
        <code value="OMIM:601374" />
        <display value="APROSENCEPHALY AND CEREBELLAR DYSGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:601375" />
        <display value="ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601376" />
        <display value="CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY" />
      </concept>
      <concept>
        <code value="OMIM:601379" />
        <display value="HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601382" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1" />
      </concept>
      <concept>
        <code value="OMIM:601386" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 12" />
      </concept>
      <concept>
        <code value="OMIM:601388" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 12" />
      </concept>
      <concept>
        <code value="OMIM:601389" />
        <display value="CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION" />
      </concept>
      <concept>
        <code value="OMIM:601390" />
        <display value="VAN MALDERGEM SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:601399" />
        <display value="PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY" />
      </concept>
      <concept>
        <code value="OMIM:601407" />
        <display value="DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2" />
      </concept>
      <concept>
        <code value="OMIM:601410" />
        <display value="DIABETES MELLITUS, TRANSIENT NEONATAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:601412" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 7" />
      </concept>
      <concept>
        <code value="OMIM:601414" />
        <display value="RETINITIS PIGMENTOSA 18" />
      </concept>
      <concept>
        <code value="OMIM:601419" />
        <display value="MYOPATHY, MYOFIBRILLAR, 1" />
      </concept>
      <concept>
        <code value="OMIM:601420" />
        <display value="MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE" />
      </concept>
      <concept>
        <code value="OMIM:601427" />
        <display value="ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS" />
      </concept>
      <concept>
        <code value="OMIM:601438" />
        <display value="RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601449" />
        <display value="DEAFNESS, PROGRESSIVE, WITH STAPES FIXATION" />
      </concept>
      <concept>
        <code value="OMIM:601450" />
        <display value="DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERS AND FACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:601452" />
        <display value="OCULOAURICULOFRONTONASAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601453" />
        <display value="TRICHODENTAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:601454" />
        <display value="PSORIASIS 3, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:601455" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D" />
      </concept>
      <concept>
        <code value="OMIM:601457" />
        <display value="SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:601458" />
        <display value="INFLAMMATORY BOWEL DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:601462" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL" />
      </concept>
      <concept>
        <code value="OMIM:601466" />
        <display value="PATENT DUCTUS VENOSUS" />
      </concept>
      <concept>
        <code value="OMIM:601471" />
        <display value="FACIAL PARESIS, HEREDITARY CONGENITAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:601472" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D" />
      </concept>
      <concept>
        <code value="OMIM:601477" />
        <display value="RIBBING DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:601492" />
        <display value="MUCOPOLYSACCHARIDOSIS, TYPE IX" />
      </concept>
      <concept>
        <code value="OMIM:601493" />
        <display value="CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION" />
      </concept>
      <concept>
        <code value="OMIM:601494" />
        <display value="CARDIOMYOPATHY, DILATED, 1D" />
      </concept>
      <concept>
        <code value="OMIM:601495" />
        <display value="AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:601499" />
        <display value="AXENFELD-RIEGER SYNDROME, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:601518" />
        <display value="PROSTATE CANCER, HEREDITARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:601536" />
        <display value="ATHABASKAN BRAINSTEM DYSGENESIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601537" />
        <display value="MICROCEPHALY, RETINITIS PIGMENTOSA, AND SUTURAL CATARACT" />
      </concept>
      <concept>
        <code value="OMIM:601539" />
        <display value="PEROXISOME BIOGENESIS DISORDER 1B" />
      </concept>
      <concept>
        <code value="OMIM:601543" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 12" />
      </concept>
      <concept>
        <code value="OMIM:601544" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 3A" />
      </concept>
      <concept>
        <code value="OMIM:601547" />
        <display value="CATARACT 3, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:601549" />
        <display value="ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:601550" />
        <display value="BLOOD GROUP--SWANN SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:601551" />
        <display value="BLOOD GROUP--FROESE" />
      </concept>
      <concept>
        <code value="OMIM:601552" />
        <display value="FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS" />
      </concept>
      <concept>
        <code value="OMIM:601553" />
        <display value="HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:601559" />
        <display value="STUVE-WIEDEMANN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601560" />
        <display value="MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE" />
      </concept>
      <concept>
        <code value="OMIM:601561" />
        <display value="DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA" />
      </concept>
      <concept>
        <code value="OMIM:601563" />
        <display value="HORNS IN SHEEP" />
      </concept>
      <concept>
        <code value="OMIM:601583" />
        <display value="WILMS TUMOR 5" />
      </concept>
      <concept>
        <code value="OMIM:601596" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C" />
      </concept>
      <concept>
        <code value="OMIM:601606" />
        <display value="TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:601608" />
        <display value="SPASTIC PARAPLEGIA AND EVANS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601612" />
        <display value="LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601616" />
        <display value="IRIS PIGMENT EPITHELIUM ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:601626" />
        <display value="LEUKEMIA, ACUTE MYELOID" />
      </concept>
      <concept>
        <code value="OMIM:601631" />
        <display value="ANTERIOR SEGMENT DYSGENESIS 3" />
      </concept>
      <concept>
        <code value="OMIM:601634" />
        <display value="NEURAL TUBE DEFECTS, FOLATE-SENSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:601650" />
        <display value="PARAGANGLIOMAS 2" />
      </concept>
      <concept>
        <code value="OMIM:601665" />
        <display value="OBESITY" />
      </concept>
      <concept>
        <code value="OMIM:601666" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 15" />
      </concept>
      <concept>
        <code value="OMIM:601668" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION" />
      </concept>
      <concept>
        <code value="OMIM:601675" />
        <display value="TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:601676" />
        <display value="ACUTE INSULIN RESPONSE" />
      </concept>
      <concept>
        <code value="OMIM:601678" />
        <display value="BARTTER SYNDROME, TYPE 1, ANTENATAL" />
      </concept>
      <concept>
        <code value="OMIM:601680" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 2B" />
      </concept>
      <concept>
        <code value="OMIM:601682" />
        <display value="GLAUCOMA 1, PRIMARY OPEN ANGLE, C" />
      </concept>
      <concept>
        <code value="OMIM:601694" />
        <display value="LEPTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:601696" />
        <display value="NOVELTY SEEKING PERSONALITY TRAIT" />
      </concept>
      <concept>
        <code value="OMIM:601700" />
        <display value="SEBACEOUS GLAND HYPERPLASIA, FAMILIAL PRESENILE" />
      </concept>
      <concept>
        <code value="OMIM:601701" />
        <display value="ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:601705" />
        <display value="T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:601706" />
        <display value="YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601707" />
        <display value="CURRY-JONES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601708" />
        <display value="SUPERIOR TRANSVERSE SCAPULAR LIGAMENT, CALCIFICATION OF, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:601709" />
        <display value="QUEBEC PLATELET DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:601718" />
        <display value="RETINITIS PIGMENTOSA 19" />
      </concept>
      <concept>
        <code value="OMIM:601744" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:601759" />
        <display value="PREAXIAL HALLUCAL POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:601764" />
        <display value="SEIZURES, BENIGN FAMILIAL INFANTILE, 1" />
      </concept>
      <concept>
        <code value="OMIM:601775" />
        <display value="FOLATE LEVEL IN ERYTHROCYTES" />
      </concept>
      <concept>
        <code value="OMIM:601776" />
        <display value="EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1" />
      </concept>
      <concept>
        <code value="OMIM:601777" />
        <display value="CONE-ROD DYSTROPHY 6" />
      </concept>
      <concept>
        <code value="OMIM:601780" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:601794" />
        <display value="COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601800" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3" />
      </concept>
      <concept>
        <code value="OMIM:601803" />
        <display value="PALLISTER-KILLIAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601808" />
        <display value="CHROMOSOME 18q DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601809" />
        <display value="SPONDYLOSPINAL THORACIC DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:601811" />
        <display value="PREMATURE AGING SYNDROME, OKAMOTO TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601812" />
        <display value="PREMATURE AGING SYNDROME, PENTTINEN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601813" />
        <display value="EXUDATIVE VITREORETINOPATHY 4" />
      </concept>
      <concept>
        <code value="OMIM:601815" />
        <display value="PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:601816" />
        <display value="BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:601820" />
        <display value="HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:601829" />
        <display value="ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:601846" />
        <display value="VACUOLAR NEUROMYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:601847" />
        <display value="CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:601853" />
        <display value="GOMEZ-LOPEZ-HERNANDEZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601859" />
        <display value="AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601868" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 13" />
      </concept>
      <concept>
        <code value="OMIM:601869" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 15" />
      </concept>
      <concept>
        <code value="OMIM:601876" />
        <display value="SPERM-SPECIFIC ANTIGEN 1" />
      </concept>
      <concept>
        <code value="OMIM:601884" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:601885" />
        <display value="CATARACT 14, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:601887" />
        <display value="MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:601888" />
        <display value="MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:601894" />
        <display value="GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2" />
      </concept>
      <concept>
        <code value="OMIM:601927" />
        <display value="LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES" />
      </concept>
      <concept>
        <code value="OMIM:601941" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 6" />
      </concept>
      <concept>
        <code value="OMIM:601942" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 10" />
      </concept>
      <concept>
        <code value="OMIM:601952" />
        <display value="KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA" />
      </concept>
      <concept>
        <code value="OMIM:601954" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 7" />
      </concept>
      <concept>
        <code value="OMIM:601957" />
        <display value="ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601976" />
        <display value="OTOFACIOOSSEOUS-GONADAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:601977" />
        <display value="THROMBOCYTHEMIA 2" />
      </concept>
      <concept>
        <code value="OMIM:601979" />
        <display value="HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION" />
      </concept>
      <concept>
        <code value="OMIM:601992" />
        <display value="FRIEDREICH ATAXIA 2" />
      </concept>
      <concept>
        <code value="OMIM:602014" />
        <display value="HYPOMAGNESEMIA 1, INTESTINAL" />
      </concept>
      <concept>
        <code value="OMIM:602025" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9" />
      </concept>
      <concept>
        <code value="OMIM:602032" />
        <display value="ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:602066" />
        <display value="CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS" />
      </concept>
      <concept>
        <code value="OMIM:602068" />
        <display value="LEISHMANIASIS, TEGUMENTARY, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:602071" />
        <display value="BROAD TERMINAL PHALANGES, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:602078" />
        <display value="FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:602079" />
        <display value="TRIMETHYLAMINURIA" />
      </concept>
      <concept>
        <code value="OMIM:602080" />
        <display value="PAGET DISEASE OF BONE 2, EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:602081" />
        <display value="SPEECH-LANGUAGE DISORDER 1" />
      </concept>
      <concept>
        <code value="OMIM:602082" />
        <display value="CORNEAL DYSTROPHY, THIEL-BEHNKE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:602083" />
        <display value="USHER SYNDROME, TYPE IF" />
      </concept>
      <concept>
        <code value="OMIM:602085" />
        <display value="POLYDACTYLY, POSTAXIAL, TYPE A2" />
      </concept>
      <concept>
        <code value="OMIM:602086" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:602087" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:602088" />
        <display value="NEPHRONOPHTHISIS 2" />
      </concept>
      <concept>
        <code value="OMIM:602089" />
        <display value="HEMANGIOMA, CAPILLARY INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:602092" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 18A" />
      </concept>
      <concept>
        <code value="OMIM:602093" />
        <display value="CONE DYSTROPHY 3" />
      </concept>
      <concept>
        <code value="OMIM:602096" />
        <display value="ALZHEIMER DISEASE 5" />
      </concept>
      <concept>
        <code value="OMIM:602097" />
        <display value="USHER SYNDROME, TYPE IE" />
      </concept>
      <concept>
        <code value="OMIM:602099" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:602107" />
        <display value="NEUROPATHY, HEREDITARY THERMOSENSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:602111" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:602114" />
        <display value="NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:602124" />
        <display value="DYSTONIA 7, TORSION" />
      </concept>
      <concept>
        <code value="OMIM:602134" />
        <display value="TREMOR, HEREDITARY ESSENTIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:602152" />
        <display value="RHYNS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602196" />
        <display value="PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:602197" />
        <display value="CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3" />
      </concept>
      <concept>
        <code value="OMIM:602199" />
        <display value="MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:602200" />
        <display value="VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY" />
      </concept>
      <concept>
        <code value="OMIM:602247" />
        <display value="XANTHOMATOSIS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:602248" />
        <display value="MALIGNANT ATROPHIC PAPULOSIS" />
      </concept>
      <concept>
        <code value="OMIM:602249" />
        <display value="PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:602252" />
        <display value="MITOCHONDRIAL INTERMEMBRANE SPACE PROTEIN TIM12, YEAST, HOMOLOG OF" />
      </concept>
      <concept>
        <code value="OMIM:602271" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL" />
      </concept>
      <concept>
        <code value="OMIM:602340" />
        <display value="SENSORINEURAL HEARING LOSS, RETINAL PIGMENT EPITHELIUM LESIONS, DISCOLORED TEETH" />
      </concept>
      <concept>
        <code value="OMIM:602342" />
        <display value="PIERPONT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602347" />
        <display value="CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:602361" />
        <display value="GRACILE BONE DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:602390" />
        <display value="HEMOCHROMATOSIS, TYPE 2A" />
      </concept>
      <concept>
        <code value="OMIM:602398" />
        <display value="DESMOSTEROLOSIS" />
      </concept>
      <concept>
        <code value="OMIM:602400" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11" />
      </concept>
      <concept>
        <code value="OMIM:602401" />
        <display value="ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:602404" />
        <display value="PARKINSON DISEASE 3, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:602418" />
        <display value="WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602429" />
        <display value="GLAUCOMA 1, OPEN ANGLE, D" />
      </concept>
      <concept>
        <code value="OMIM:602433" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:602440" />
        <display value="AMYOTROPHY, MONOMELIC" />
      </concept>
      <concept>
        <code value="OMIM:602450" />
        <display value="SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION" />
      </concept>
      <concept>
        <code value="OMIM:602459" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 15" />
      </concept>
      <concept>
        <code value="OMIM:602471" />
        <display value="SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, AND SKELETAL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:602472" />
        <display value="CREASES, INFRA-AURICULAR CUTANEOUS, WITH TALL STATURE AND ADVANCED BONE AGE" />
      </concept>
      <concept>
        <code value="OMIM:602473" />
        <display value="ENCEPHALOPATHY, ETHYLMALONIC" />
      </concept>
      <concept>
        <code value="OMIM:602475" />
        <display value="OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE" />
      </concept>
      <concept>
        <code value="OMIM:602477" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:602481" />
        <display value="MIGRAINE, FAMILIAL HEMIPLEGIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:602482" />
        <display value="AXENFELD-RIEGER SYNDROME, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:602483" />
        <display value="AURICULOCONDYLAR SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:602484" />
        <display value="PELVIC HYPOPLASIA WITH LOWER-LIMB ARTHROGRYPOSIS" />
      </concept>
      <concept>
        <code value="OMIM:602485" />
        <display value="HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:602491" />
        <display value="HYPERLIPIDEMIA, COMBINED, 1" />
      </concept>
      <concept>
        <code value="OMIM:602497" />
        <display value="CHONDRODYSPLASIA PUNCTATA, BRACHYTELEPHALANGIC, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:602499" />
        <display value="MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA" />
      </concept>
      <concept>
        <code value="OMIM:602501" />
        <display value="MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602511" />
        <display value="PSEUDOACROMEGALY WITH SEVERE INSULIN RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:602522" />
        <display value="BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:602531" />
        <display value="GRANGE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602535" />
        <display value="MARSHALL-SMITH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602540" />
        <display value="ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:602541" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:602551" />
        <display value="JEJUNAL ATRESIA WITH RENAL ADYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:602553" />
        <display value="ANAL ATRESIA, HYPOSPADIAS, AND PENOSCROTAL INVERSION" />
      </concept>
      <concept>
        <code value="OMIM:602554" />
        <display value="TORSION DYSTONIA WITH ONSET IN INFANCY" />
      </concept>
      <concept>
        <code value="OMIM:602555" />
        <display value="MICROCEPHALY, MACROTIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:602556" />
        <display value="FACIAL DYSMORPHISM, CLEFT PALATE, HEARING LOSS, AND CAMPTODACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:602557" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE" />
      </concept>
      <concept>
        <code value="OMIM:602558" />
        <display value="CRANIOMICROMELIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602561" />
        <display value="BRACHYDACTYLY, INTRAVENTRICULAR SEPTAL DEFECT, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:602562" />
        <display value="MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA" />
      </concept>
      <concept>
        <code value="OMIM:602564" />
        <display value="EMPHYSEMA, CONGENITAL, WITH DEAFNESS, PENOSCROTAL WEB, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:602579" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib" />
      </concept>
      <concept>
        <code value="OMIM:602588" />
        <display value="BRANCHIOOTIC SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:602594" />
        <display value="RETINITIS PIGMENTOSA 22" />
      </concept>
      <concept>
        <code value="OMIM:602596" />
        <display value="PANCREATIC LYMPHOMA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:602611" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA WITH CORONAL CRANIOSYNOSTOSIS, CATARACTS, CLEFT PALATE, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:602612" />
        <display value="CAMPTODACTYLY, MYOPIA, AND FIBROSIS OF THE MEDIAL RECTUS MUSCLE OF EYE" />
      </concept>
      <concept>
        <code value="OMIM:602613" />
        <display value="SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:602629" />
        <display value="DYSTONIA 6, TORSION" />
      </concept>
      <concept>
        <code value="OMIM:602639" />
        <display value="TOOTH AGENESIS, SELECTIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:602668" />
        <display value="MYOTONIC DYSTROPHY 2" />
      </concept>
      <concept>
        <code value="OMIM:602685" />
        <display value="MENTAL RETARDATION, SEVERE, WITH SPASTICITY AND PIGMENTARY TAPETORETINAL DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:602722" />
        <display value="RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:602723" />
        <display value="PSORIASIS 2" />
      </concept>
      <concept>
        <code value="OMIM:602759" />
        <display value="PROSTATE CANCER, HEREDITARY, 8" />
      </concept>
      <concept>
        <code value="OMIM:602771" />
        <display value="RIGID SPINE MUSCULAR DYSTROPHY 1" />
      </concept>
      <concept>
        <code value="OMIM:602772" />
        <display value="RETINITIS PIGMENTOSA 25" />
      </concept>
      <concept>
        <code value="OMIM:602782" />
        <display value="HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602849" />
        <display value="MUENKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:602875" />
        <display value="ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE" />
      </concept>
      <concept>
        <code value="OMIM:602966" />
        <display value="OROFACIAL CLEFT 2" />
      </concept>
      <concept>
        <code value="OMIM:602994" />
        <display value="LEUKOREGULIN" />
      </concept>
      <concept>
        <code value="OMIM:603003" />
        <display value="BILE DUCT CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:603010" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 17" />
      </concept>
      <concept>
        <code value="OMIM:603013" />
        <display value="SCHIZOPHRENIA 6" />
      </concept>
      <concept>
        <code value="OMIM:603034" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:603040" />
        <display value="TUMOR SUPPRESSOR GENE ON CHROMOSOME 11" />
      </concept>
      <concept>
        <code value="OMIM:603041" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:603047" />
        <display value="ASTIGMATISM" />
      </concept>
      <concept>
        <code value="OMIM:603075" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 1" />
      </concept>
      <concept>
        <code value="OMIM:603098" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 13" />
      </concept>
      <concept>
        <code value="OMIM:603116" />
        <display value="CDAGS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:603117" />
        <display value="SPASTIC PARAPLEGIA, OPTIC ATROPHY, MICROCEPHALY, AND XY SEX REVERSAL" />
      </concept>
      <concept>
        <code value="OMIM:603119" />
        <display value="APRAXIA OF EYELID OPENING" />
      </concept>
      <concept>
        <code value="OMIM:603133" />
        <display value="DISLOCATED ELBOWS, BOWED TIBIAS, SCOLIOSIS, DEAFNESS, CATARACT, MICROCEPHALY, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:603147" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic" />
      </concept>
      <concept>
        <code value="OMIM:603165" />
        <display value="DERMATITIS, ATOPIC" />
      </concept>
      <concept>
        <code value="OMIM:603174" />
        <display value="HOMOCYSTEINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:603175" />
        <display value="SCHIZOPHRENIA 5" />
      </concept>
      <concept>
        <code value="OMIM:603176" />
        <display value="SCHIZOPHRENIA 7" />
      </concept>
      <concept>
        <code value="OMIM:603188" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8" />
      </concept>
      <concept>
        <code value="OMIM:603194" />
        <display value="MECKEL SYNDROME, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:603204" />
        <display value="EPILEPSY, NOCTURNAL FRONTAL LOBE, 2" />
      </concept>
      <concept>
        <code value="OMIM:603206" />
        <display value="SCHIZOPHRENIA 8" />
      </concept>
      <concept>
        <code value="OMIM:603209" />
        <display value="CYTIDINE MONOPHOSPHO-N-ACETYLNEURAMINIC ACID HYDROXYLASE, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:603218" />
        <display value="HUNTINGTON DISEASE-LIKE 1" />
      </concept>
      <concept>
        <code value="OMIM:603221" />
        <display value="MYOPIA 3, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:603233" />
        <display value="PSEUDOHYPOPARATHYROIDISM, TYPE IB" />
      </concept>
      <concept>
        <code value="OMIM:603266" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 17" />
      </concept>
      <concept>
        <code value="OMIM:603278" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:603282" />
        <display value="ZINC FINGER PROTEIN 204" />
      </concept>
      <concept>
        <code value="OMIM:603284" />
        <display value="CEREBRAL CAVERNOUS MALFORMATIONS 2" />
      </concept>
      <concept>
        <code value="OMIM:603285" />
        <display value="CEREBRAL CAVERNOUS MALFORMATIONS 3" />
      </concept>
      <concept>
        <code value="OMIM:603323" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, WITH CEREBELLAR ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:603324" />
        <display value="GAP JUNCTION PROTEIN, BETA-3" />
      </concept>
      <concept>
        <code value="OMIM:603342" />
        <display value="SCHIZOPHRENIA 2" />
      </concept>
      <concept>
        <code value="OMIM:603358" />
        <display value="GRACILE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:603372" />
        <display value="THYROID-STIMULATING HORMONE RECEPTOR" />
      </concept>
      <concept>
        <code value="OMIM:603373" />
        <display value="HYPERTHYROIDISM, FAMILIAL GESTATIONAL" />
      </concept>
      <concept>
        <code value="OMIM:603376" />
        <display value="LONG CHAIN FATTY ACIDS, DEFECT IN TRANSPORT OF" />
      </concept>
      <concept>
        <code value="OMIM:603383" />
        <display value="GLAUCOMA 1, OPEN ANGLE, F" />
      </concept>
      <concept>
        <code value="OMIM:603386" />
        <display value="THYROID CARCINOMA, NONMEDULLARY, WITH OR WITHOUT CELL OXYPHILIA" />
      </concept>
      <concept>
        <code value="OMIM:603387" />
        <display value="MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:603388" />
        <display value="GRAVES DISEASE, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:603389" />
        <display value="OSEBOLD SKELETAL DYSPLASIA/OSTEOLYSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:603393" />
        <display value="OSTEOSCLEROTIC CHONDRODYSPLASIA, LETHAL, WITH INTRACELLULAR INCLUSIONS" />
      </concept>
      <concept>
        <code value="OMIM:603394" />
        <display value="MICROCEPHALY, SEVERE, WITH SKELETAL ANOMALIES INCLUDING POSTERIOR RIB-GAP DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:603396" />
        <display value="TONOKI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:603416" />
        <display value="RIBOSOMAL PROTEIN L21 PSEUDOGENE 1" />
      </concept>
      <concept>
        <code value="OMIM:603438" />
        <display value="RADIOULNAR SYNOSTOSIS WITH MICROCEPHALY, SHORT STATURE, SCOLIOSIS, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:603439" />
        <display value="EXPANSILE BONE LESIONS" />
      </concept>
      <concept>
        <code value="OMIM:603446" />
        <display value="OROACRAL SYNDROME, VERLOES-KOULISCHER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:603457" />
        <display value="BOSMA ARHINIA MICROPHTHALMIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:603467" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP F" />
      </concept>
      <concept>
        <code value="OMIM:603471" />
        <display value="CITRULLINEMIA, TYPE II, ADULT-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:603472" />
        <display value="NEURONAL INTRANUCLEAR INCLUSION DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:603511" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:603513" />
        <display value="CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:603516" />
        <display value="SPINOCEREBELLAR ATAXIA 10" />
      </concept>
      <concept>
        <code value="OMIM:603523" />
        <display value="CHYLOTHORAX, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:603529" />
        <display value="DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLAST HETEROCHROMATIN" />
      </concept>
      <concept>
        <code value="OMIM:603530" />
        <display value="LIGHT FIXATION SEIZURE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:603543" />
        <display value="LIMB-MAMMARY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:603546" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:603552" />
        <display value="HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:603553" />
        <display value="HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:603554" />
        <display value="OMENN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:603563" />
        <display value="SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:603569" />
        <display value="TRACHEOBRONCHIAL STENOSIS, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:603570" />
        <display value="VANIN 1" />
      </concept>
      <concept>
        <code value="OMIM:603572" />
        <display value="MICROCEPHALY, FACIAL ABNORMALITIES, MICROMELIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:603585" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf" />
      </concept>
      <concept>
        <code value="OMIM:603587" />
        <display value="FOLLICULAR ATROPHODERMA, PERIORAL PIGMENTED, WITH MILIA AND EPIDERMOID CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:603588" />
        <display value="PAROTITIS, JUVENILE RECURRENT" />
      </concept>
      <concept>
        <code value="OMIM:603589" />
        <display value="FACIAL DYSMORPHISM, SELECTIVE TOOTH AGENESIS, AND CHOROID CALCIFICATION" />
      </concept>
      <concept>
        <code value="OMIM:603592" />
        <display value="XANTHINURIA, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:603595" />
        <display value="CRANIOSYNOSTOSIS WITH ECTOPIA LENTIS" />
      </concept>
      <concept>
        <code value="OMIM:603596" />
        <display value="POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:603600" />
        <display value="OSTEOMA OF CRANIAL VAULT, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:603622" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 17" />
      </concept>
      <concept>
        <code value="OMIM:603629" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 21" />
      </concept>
      <concept>
        <code value="OMIM:603641" />
        <display value="NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:603642" />
        <display value="ATRIAL SEPTAL DEFECT, SECUNDUM, WITH VARIOUS CARDIAC AND NONCARDIAC DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:603643" />
        <display value="SITUS INVERSUS TOTALIS WITH CYSTIC DYSPLASIA OF KIDNEYS AND PANCREAS" />
      </concept>
      <concept>
        <code value="OMIM:603649" />
        <display value="CONE-ROD DYSTROPHY 7" />
      </concept>
      <concept>
        <code value="OMIM:603656" />
        <display value="EXOSTOSIS, DUPUYTREN SUBUNGUAL" />
      </concept>
      <concept>
        <code value="OMIM:603663" />
        <display value="MENTAL HEALTH WELLNESS 1" />
      </concept>
      <concept>
        <code value="OMIM:603664" />
        <display value="MENTAL HEALTH WELLNESS 2" />
      </concept>
      <concept>
        <code value="OMIM:603669" />
        <display value="ECCRINE SYRINGOFIBROADENOMATOSIS WITH EYELID ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:603670" />
        <display value="BLUE NEVI, FAMILIAL MULTIPLE" />
      </concept>
      <concept>
        <code value="OMIM:603671" />
        <display value="ACROMELIC FRONTONASAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:603678" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 14" />
      </concept>
      <concept>
        <code value="OMIM:603688" />
        <display value="PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY" />
      </concept>
      <concept>
        <code value="OMIM:603689" />
        <display value="HEREDITARY MYOPATHY WITH EARLY RESPIRATORY FAILURE" />
      </concept>
      <concept>
        <code value="OMIM:603694" />
        <display value="DIABETES MELLITUS, NONINSULIN-DEPENDENT, 3" />
      </concept>
      <concept>
        <code value="OMIM:603720" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 16" />
      </concept>
      <concept>
        <code value="OMIM:603736" />
        <display value="OHDO SYNDROME, SBBYS VARIANT" />
      </concept>
      <concept>
        <code value="OMIM:603737" />
        <display value="OVARIAN GERM CELL CANCER" />
      </concept>
      <concept>
        <code value="OMIM:603740" />
        <display value="ACRODYSPLASIA WITH OSSIFICATION ABNORMALITIES, SHORT STATURE, AND FIBULAR HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:603744" />
        <display value="PAPILLARY THYROID MICROCARCINOMA" />
      </concept>
      <concept>
        <code value="OMIM:603776" />
        <display value="HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3" />
      </concept>
      <concept>
        <code value="OMIM:603783" />
        <display value="INTELLIGENCE QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:603786" />
        <display value="STARGARDT DISEASE 4" />
      </concept>
      <concept>
        <code value="OMIM:603794" />
        <display value="HYDROA VACCINIFORME, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:603802" />
        <display value="MICROCEPHALY WITH SIMPLIFIED GYRAL PATTERN" />
      </concept>
      <concept>
        <code value="OMIM:603806" />
        <display value="URINARY TRACT INFECTIONS, RECURRENT, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:603813" />
        <display value="HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:603828" />
        <display value="BRITTLE BONE DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:603829" />
        <display value="VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:603830" />
        <display value="LONG QT SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:603855" />
        <display value="CYSTIC FIBROSIS, MODIFIER OF, 1" />
      </concept>
      <concept>
        <code value="OMIM:603860" />
        <display value="MEDULLARY CYSTIC KIDNEY DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:603896" />
        <display value="LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER" />
      </concept>
      <concept>
        <code value="OMIM:603902" />
        <display value="BETA-THALASSEMIA, DOMINANT INCLUSION BODY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:603903" />
        <display value="SICKLE CELL ANEMIA" />
      </concept>
      <concept>
        <code value="OMIM:603909" />
        <display value="AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA" />
      </concept>
      <concept>
        <code value="OMIM:603918" />
        <display value="HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:603932" />
        <display value="INTERVERTEBRAL DISC DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:603933" />
        <display value="MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:603935" />
        <display value="PSORIASIS 4, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:603956" />
        <display value="CERVICAL CANCER" />
      </concept>
      <concept>
        <code value="OMIM:603964" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 16" />
      </concept>
      <concept>
        <code value="OMIM:603965" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:604004" />
        <display value="MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1" />
      </concept>
      <concept>
        <code value="OMIM:604011" />
        <display value="UNC119, C. ELEGANS, HOMOLOG OF" />
      </concept>
      <concept>
        <code value="OMIM:604060" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 20" />
      </concept>
      <concept>
        <code value="OMIM:604091" />
        <display value="HYPOALPHALIPOPROTEINEMIA, PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:604093" />
        <display value="KERATOSIS PILARIS ATROPHICANS" />
      </concept>
      <concept>
        <code value="OMIM:604116" />
        <display value="CONE-ROD DYSTROPHY 3" />
      </concept>
      <concept>
        <code value="OMIM:604117" />
        <display value="VOHWINKEL SYNDROME, VARIANT FORM" />
      </concept>
      <concept>
        <code value="OMIM:604121" />
        <display value="CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:604129" />
        <display value="EPIDERMOLYSIS BULLOSA PRURIGINOSA" />
      </concept>
      <concept>
        <code value="OMIM:604131" />
        <display value="ALPHA-THALASSEMIA" />
      </concept>
      <concept>
        <code value="OMIM:604145" />
        <display value="CARDIOMYOPATHY, DILATED, 1G" />
      </concept>
      <concept>
        <code value="OMIM:604154" />
        <display value="ALZHEIMER DISEASE WITHOUT NEUROFIBRILLARY TANGLES" />
      </concept>
      <concept>
        <code value="OMIM:604168" />
        <display value="CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:604169" />
        <display value="LEFT VENTRICULAR NONCOMPACTION 1" />
      </concept>
      <concept>
        <code value="OMIM:604172" />
        <display value="CARONTE" />
      </concept>
      <concept>
        <code value="OMIM:604173" />
        <display value="POIKILODERMA WITH NEUTROPENIA" />
      </concept>
      <concept>
        <code value="OMIM:604183" />
        <display value="CHOLESTEATOMA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:604185" />
        <display value="FACIAL PARESIS, HEREDITARY CONGENITAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:604187" />
        <display value="SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:604201" />
        <display value="HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION" />
      </concept>
      <concept>
        <code value="OMIM:604211" />
        <display value="HIRSCHSPRUNG DISEASE WITH HEART DEFECTS, LARYNGEAL ANOMALIES, AND PREAXIAL POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:604213" />
        <display value="CHUDLEY-MCCULLOUGH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:604218" />
        <display value="ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES" />
      </concept>
      <concept>
        <code value="OMIM:604219" />
        <display value="CATARACT 9, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:604229" />
        <display value="ANTERIOR SEGMENT DYSGENESIS 5" />
      </concept>
      <concept>
        <code value="OMIM:604232" />
        <display value="LEBER CONGENITAL AMAUROSIS 3" />
      </concept>
      <concept>
        <code value="OMIM:604233" />
        <display value="GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:604250" />
        <display value="HEMOCHROMATOSIS, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:604254" />
        <display value="DYSLEXIA, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:604257" />
        <display value="CAMERA-MARUGO-COHEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:604271" />
        <display value="GROWTH HORMONE INSENSITIVITY, PARTIAL" />
      </concept>
      <concept>
        <code value="OMIM:604273" />
        <display value="MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:604278" />
        <display value="RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:604286" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 4" />
      </concept>
      <concept>
        <code value="OMIM:604287" />
        <display value="CARNEY TRIAD" />
      </concept>
      <concept>
        <code value="OMIM:604288" />
        <display value="CARDIOMYOPATHY, DILATED, 1H" />
      </concept>
      <concept>
        <code value="OMIM:604290" />
        <display value="ACERULOPLASMINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:604291" />
        <display value="ASCARIS LUMBRICOIDES INFECTION, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:604292" />
        <display value="ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:604302" />
        <display value="RHEUMATOID ARTHRITIS, SYSTEMIC JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:604307" />
        <display value="CATARACT 2, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:604308" />
        <display value="MASS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:604314" />
        <display value="BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:604315" />
        <display value="ANEMIA, CONGENITAL HYPOPLASTIC, WITH MULTIPLE CONGENITAL ANOMALIES/MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:604316" />
        <display value="PSORIASIS 5, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:604317" />
        <display value="MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:604320" />
        <display value="SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:604321" />
        <display value="MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:604324" />
        <display value="ACNE, ADULT" />
      </concept>
      <concept>
        <code value="OMIM:604326" />
        <display value="SPINOCEREBELLAR ATAXIA 12" />
      </concept>
      <concept>
        <code value="OMIM:604329" />
        <display value="HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:604335" />
        <display value="REFLEX SYMPATHETIC DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:604348" />
        <display value="ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:604352" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:604356" />
        <display value="DUANE RETRACTION SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:604360" />
        <display value="SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:604363" />
        <display value="MYOCLONIC EPILEPSY, CONGENITAL DEAFNESS, MACULAR DYSTROPHY, AND PSYCHIATRIC DISORDERS" />
      </concept>
      <concept>
        <code value="OMIM:604364" />
        <display value="EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1" />
      </concept>
      <concept>
        <code value="OMIM:604367" />
        <display value="LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:604369" />
        <display value="SALLA DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:604370" />
        <display value="BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:604373" />
        <display value="CHECKPOINT KINASE 2, S. POMBE, HOMOLOG OF" />
      </concept>
      <concept>
        <code value="OMIM:604377" />
        <display value="CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1" />
      </concept>
      <concept>
        <code value="OMIM:604379" />
        <display value="HYPOTRICHOSIS 7" />
      </concept>
      <concept>
        <code value="OMIM:604380" />
        <display value="ULNAR RAY DYSGENESIS WITH POSTAXIAL POLYDACTYLY AND RENAL CYSTIC DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:604381" />
        <display value="PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:604382" />
        <display value="LISSENCEPHALY, FAMILIAL, WITH CLEFT PALATE AND CEREBELLAR HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:604387" />
        <display value="NEPHRONOPHTHISIS 3" />
      </concept>
      <concept>
        <code value="OMIM:604391" />
        <display value="ATAXIA-TELANGIECTASIA-LIKE DISORDER 1" />
      </concept>
      <concept>
        <code value="OMIM:604393" />
        <display value="LEBER CONGENITAL AMAUROSIS 4" />
      </concept>
      <concept>
        <code value="OMIM:604400" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:604401" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:604403" />
        <display value="GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:604416" />
        <display value="PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE" />
      </concept>
      <concept>
        <code value="OMIM:604431" />
        <display value="POLYNEUROPATHY, LETHAL NEONATAL, AXONAL SENSORIMOTOR, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:604432" />
        <display value="SPINOCEREBELLAR ATAXIA 11" />
      </concept>
      <concept>
        <code value="OMIM:604451" />
        <display value="BASAL CELL CARCINOMA, INFUNDIBULOCYSTIC" />
      </concept>
      <concept>
        <code value="OMIM:604454" />
        <display value="WELANDER DISTAL MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:604474" />
        <display value="HUMAN HERPESVIRUS TYPE 6, INTEGRATED" />
      </concept>
      <concept>
        <code value="OMIM:604484" />
        <display value="NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:604498" />
        <display value="AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:604499" />
        <display value="HYPERLIPIDEMIA, COMBINED, 2" />
      </concept>
      <concept>
        <code value="OMIM:604519" />
        <display value="INFLAMMATORY BOWEL DISEASE 3" />
      </concept>
      <concept>
        <code value="OMIM:604536" />
        <display value="ECTODERMAL DYSPLASIA/SKIN FRAGILITY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:604537" />
        <display value="LEBER CONGENITAL AMAUROSIS 5" />
      </concept>
      <concept>
        <code value="OMIM:604547" />
        <display value="VAN DER WOUDE SYNDROME 1, MODIFIER OF" />
      </concept>
      <concept>
        <code value="OMIM:604559" />
        <display value="PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB" />
      </concept>
      <concept>
        <code value="OMIM:604563" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2" />
      </concept>
      <concept>
        <code value="OMIM:604571" />
        <display value="BARE LYMPHOCYTE SYNDROME, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:604595" />
        <display value="CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:604625" />
        <display value="TOOTH AGENESIS, SELECTIVE, 3" />
      </concept>
      <concept>
        <code value="OMIM:604690" />
        <display value="GROWTH AND DEVELOPMENTAL RETARDATION, OCULAR PTOSIS, CARDIAC DEFECT, AND ANAL ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:604715" />
        <display value="ORTHOSTATIC INTOLERANCE" />
      </concept>
      <concept>
        <code value="OMIM:604717" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 20" />
      </concept>
      <concept>
        <code value="OMIM:604757" />
        <display value="CRANIOSYNOSTOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:604765" />
        <display value="CARDIOMYOPATHY, DILATED, 1I" />
      </concept>
      <concept>
        <code value="OMIM:604771" />
        <display value="POLYCYSTIC BONE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:604772" />
        <display value="VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:604777" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5" />
      </concept>
      <concept>
        <code value="OMIM:604801" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, 1B" />
      </concept>
      <concept>
        <code value="OMIM:604802" />
        <display value="HUNTINGTON DISEASE-LIKE 3" />
      </concept>
      <concept>
        <code value="OMIM:604804" />
        <display value="MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:604805" />
        <display value="SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:604809" />
        <display value="PANBRONCHIOLITIS, DIFFUSE" />
      </concept>
      <concept>
        <code value="OMIM:604827" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:604830" />
        <display value="MANDIBULOFACIAL DYSOSTOSIS SYNDROME, BAURU TYPE" />
      </concept>
      <concept>
        <code value="OMIM:604841" />
        <display value="STICKLER SYNDROME, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:604855" />
        <display value="HYALURONAN METABOLISM, DEFECT IN" />
      </concept>
      <concept>
        <code value="OMIM:604856" />
        <display value="LANGERHANS CELL HISTIOCYTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:604864" />
        <display value="OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:604901" />
        <display value="NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS" />
      </concept>
      <concept>
        <code value="OMIM:604906" />
        <display value="SCHIZOPHRENIA 9" />
      </concept>
      <concept>
        <code value="OMIM:604916" />
        <display value="HYDRONEPHROSIS, CONGENITAL, WITH CLEFT PALATE, CHARACTERISTIC FACIES, HYPOTONIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:604919" />
        <display value="BECKER NEVUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:604922" />
        <display value="CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA" />
      </concept>
      <concept>
        <code value="OMIM:604928" />
        <display value="WOLFRAM SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:604931" />
        <display value="CORTISONE REDUCTASE DEFICIENCY 1" />
      </concept>
      <concept>
        <code value="OMIM:604966" />
        <display value="PROTOCADHERIN-ALPHA GENE CLUSTER" />
      </concept>
      <concept>
        <code value="OMIM:604967" />
        <display value="PROTOCADHERIN-BETA GENE CLUSTER" />
      </concept>
      <concept>
        <code value="OMIM:604968" />
        <display value="PROTOCADHERIN-GAMMA GENE CLUSTER" />
      </concept>
      <concept>
        <code value="OMIM:604976" />
        <display value="PROTEIN KINASE, AMP-ACTIVATED, NONCATALYTIC, GAMMA-3" />
      </concept>
      <concept>
        <code value="OMIM:605013" />
        <display value="MICROHYDRANENCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:605019" />
        <display value="HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:605021" />
        <display value="MYOCLONIC EPILEPSY, FAMILIAL INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:605026" />
        <display value="DIABETES MELLITUS, CONGENITAL AUTOIMMUNE" />
      </concept>
      <concept>
        <code value="OMIM:605027" />
        <display value="LYMPHOMA, NON-HODGKIN, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:605028" />
        <display value="LOW DENSITY LIPOPROTEIN CHOLESTEROL, MILD ELEVATION OF" />
      </concept>
      <concept>
        <code value="OMIM:605039" />
        <display value="BOHRING-OPITZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605040" />
        <display value="CLAVICULAR HYPOPLASIA, ZYGOMATIC ARCH HYPOPLASIA, AND MICROGNATHIA" />
      </concept>
      <concept>
        <code value="OMIM:605041" />
        <display value="BROOKE-SPIEGLER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605055" />
        <display value="ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID AND PRION PATHOLOGY" />
      </concept>
      <concept>
        <code value="OMIM:605067" />
        <display value="TRICUSPID ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:605074" />
        <display value="RENAL CELL CARCINOMA, PAPILLARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:605105" />
        <display value="EARLY RESPONSE TO NEURAL INDUCTION GENE" />
      </concept>
      <concept>
        <code value="OMIM:605115" />
        <display value="HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH SEVERE EXACERBATION IN PREGNANCY" />
      </concept>
      <concept>
        <code value="OMIM:605130" />
        <display value="WIEDEMANN-STEINER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605192" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 23" />
      </concept>
      <concept>
        <code value="OMIM:605201" />
        <display value="HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 14" />
      </concept>
      <concept>
        <code value="OMIM:605218" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:605225" />
        <display value="INFLAMMATORY BOWEL DISEASE 7" />
      </concept>
      <concept>
        <code value="OMIM:605229" />
        <display value="SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:605231" />
        <display value="BARDET-BIEDL SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:605233" />
        <display value="DIANZANI AUTOIMMUNE LYMPHOPROLIFERATIVE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:605244" />
        <display value="CARNEY COMPLEX, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:605253" />
        <display value="NEUROPATHY, CONGENITAL HYPOMYELINATING OR AMYELINATING, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:605258" />
        <display value="IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:605259" />
        <display value="SPINOCEREBELLAR ATAXIA 13" />
      </concept>
      <concept>
        <code value="OMIM:605274" />
        <display value="MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:605275" />
        <display value="NOONAN SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:605280" />
        <display value="SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:605282" />
        <display value="TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605285" />
        <display value="NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:605289" />
        <display value="SPLIT-HAND/FOOT MALFORMATION 4" />
      </concept>
      <concept>
        <code value="OMIM:605293" />
        <display value="OPTIC ATROPHY 4" />
      </concept>
      <concept>
        <code value="OMIM:605309" />
        <display value="MACROCEPHALY/AUTISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605321" />
        <display value="FRONTOOCULAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605355" />
        <display value="NEMALINE MYOPATHY 5" />
      </concept>
      <concept>
        <code value="OMIM:605361" />
        <display value="SPINOCEREBELLAR ATAXIA 14" />
      </concept>
      <concept>
        <code value="OMIM:605362" />
        <display value="CARDIOMYOPATHY, DILATED, 1J" />
      </concept>
      <concept>
        <code value="OMIM:605364" />
        <display value="PSORIASIS 6, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:605373" />
        <display value="PARAGANGLIOMAS 3" />
      </concept>
      <concept>
        <code value="OMIM:605375" />
        <display value="EPILEPSY, NOCTURNAL FRONTAL LOBE, 3" />
      </concept>
      <concept>
        <code value="OMIM:605376" />
        <display value="HETEROTAXY, VISCERAL, 2, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:605387" />
        <display value="CATARACT 31, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:605388" />
        <display value="CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:605389" />
        <display value="HYPOTRICHOSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:605400" />
        <display value="FIBROMATOSIS, GINGIVAL, WITH HYPERTRICHOSIS AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:605407" />
        <display value="SEGAWA SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:605419" />
        <display value="SCHIZOPHRENIA 10" />
      </concept>
      <concept>
        <code value="OMIM:605428" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 26" />
      </concept>
      <concept>
        <code value="OMIM:605429" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 26, MODIFIER OF" />
      </concept>
      <concept>
        <code value="OMIM:605432" />
        <display value="RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 1" />
      </concept>
      <concept>
        <code value="OMIM:605462" />
        <display value="BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:605463" />
        <display value="RADIATION SENSITIVITY/CHROMOSOME INSTABILITY SYNDROME, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:605472" />
        <display value="USHER SYNDROME, TYPE IIC" />
      </concept>
      <concept>
        <code value="OMIM:605479" />
        <display value="CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:605480" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:605526" />
        <display value="ALZHEIMER DISEASE 6" />
      </concept>
      <concept>
        <code value="OMIM:605543" />
        <display value="PARKINSON DISEASE 4, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:605544" />
        <display value="FIBROMATOSIS, GINGIVAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:605549" />
        <display value="CONE-ROD DYSTROPHY 8" />
      </concept>
      <concept>
        <code value="OMIM:605552" />
        <display value="ABDOMINAL OBESITY-METABOLIC SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:605572" />
        <display value="ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:605582" />
        <display value="CARDIOMYOPATHY, DILATED, 1K" />
      </concept>
      <concept>
        <code value="OMIM:605583" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 25" />
      </concept>
      <concept>
        <code value="OMIM:605588" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1" />
      </concept>
      <concept>
        <code value="OMIM:605589" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2" />
      </concept>
      <concept>
        <code value="OMIM:605594" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1" />
      </concept>
      <concept>
        <code value="OMIM:605598" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 18" />
      </concept>
      <concept>
        <code value="OMIM:605606" />
        <display value="PSORIASIS 7, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:605618" />
        <display value="TETRALOGY OF FALLOT SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:605627" />
        <display value="CEREBROOCULONASAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605635" />
        <display value="HYPERALDOSTERONISM, FAMILIAL, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:605637" />
        <display value="MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA" />
      </concept>
      <concept>
        <code value="OMIM:605642" />
        <display value="THYROID CARCINOMA, PAPILLARY, WITH PAPILLARY RENAL NEOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:605670" />
        <display value="LATE-ONSET RETINAL DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:605672" />
        <display value="CEREBELLAR ATAXIA AND HYPERGONADOTROPIC HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:605676" />
        <display value="CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA" />
      </concept>
      <concept>
        <code value="OMIM:605711" />
        <display value="MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:605714" />
        <display value="CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:605724" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP D1" />
      </concept>
      <concept>
        <code value="OMIM:605726" />
        <display value="SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:605727" />
        <display value="OTOSCLEROSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:605728" />
        <display value="CATARACT 25" />
      </concept>
      <concept>
        <code value="OMIM:605735" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 12" />
      </concept>
      <concept>
        <code value="OMIM:605738" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 2" />
      </concept>
      <concept>
        <code value="OMIM:605746" />
        <display value="ANISOMASTIA" />
      </concept>
      <concept>
        <code value="OMIM:605749" />
        <display value="CATARACT 26, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:605750" />
        <display value="EXUDATIVE VITREORETINOPATHY 3" />
      </concept>
      <concept>
        <code value="OMIM:605751" />
        <display value="SEIZURES, BENIGN FAMILIAL INFANTILE, 2" />
      </concept>
      <concept>
        <code value="OMIM:605756" />
        <display value="OVARIAN DYSGENESIS, HYPERGONADOTROPIC, WITH SHORT STATURE AND RECURRENT METABOLIC ACIDOSIS" />
      </concept>
      <concept>
        <code value="OMIM:605779" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 7" />
      </concept>
      <concept>
        <code value="OMIM:605803" />
        <display value="DERMATITIS, ATOPIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:605804" />
        <display value="DERMATITIS, ATOPIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:605805" />
        <display value="DERMATITIS, ATOPIC, 4" />
      </concept>
      <concept>
        <code value="OMIM:605808" />
        <display value="BIRDSHOT CHORIORETINOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:605809" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL" />
      </concept>
      <concept>
        <code value="OMIM:605814" />
        <display value="CITRULLINEMIA, TYPE II, NEONATAL-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:605818" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 27" />
      </concept>
      <concept>
        <code value="OMIM:605820" />
        <display value="NONAKA MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:605822" />
        <display value="SPONDYLOOCULAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605827" />
        <display value="BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:605833" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:605838" />
        <display value="BABY RATTLE PELVIS DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:605841" />
        <display value="NARCOLEPSY 2, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:605844" />
        <display value="DERMATITIS, ATOPIC, 5" />
      </concept>
      <concept>
        <code value="OMIM:605845" />
        <display value="DERMATITIS, ATOPIC, 6" />
      </concept>
      <concept>
        <code value="OMIM:605850" />
        <display value="DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:605856" />
        <display value="SHORT STATURE, MENTAL RETARDATION, CALLOSAL AGENESIS, HEMINASAL HYPOPLASIA, MICROPHTHALMIA, AND ATYPICAL CLEFTING" />
      </concept>
      <concept>
        <code value="OMIM:605899" />
        <display value="GLYCINE ENCEPHALOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:605909" />
        <display value="PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:605911" />
        <display value="3-HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE-2 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:605913" />
        <display value="BLEEDING DISORDER, EAST TEXAS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:605934" />
        <display value="HOLOPROSENCEPHALY 6" />
      </concept>
      <concept>
        <code value="OMIM:605935" />
        <display value="ARTHROPATHY, EROSIVE" />
      </concept>
      <concept>
        <code value="OMIM:605944" />
        <display value="LIVER FIBROCYSTIC DISEASE AND POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:605945" />
        <display value="CRUMPLED HELICES AND SMALL MOUTH" />
      </concept>
      <concept>
        <code value="OMIM:605946" />
        <display value="METAPHYSEAL DYSPLASIA, BRAUN-TINSCHERT TYPE" />
      </concept>
      <concept>
        <code value="OMIM:605967" />
        <display value="ACROPECTORAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:605990" />
        <display value="NEPHROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:606002" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1" />
      </concept>
      <concept>
        <code value="OMIM:606003" />
        <display value="TRANSALDOLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:606012" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 18" />
      </concept>
      <concept>
        <code value="OMIM:606035" />
        <display value="FASTING INSULIN LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:606049" />
        <display value="ACROMEGALOID FEATURES, OVERGROWTH, CLEFT PALATE, AND HERNIA" />
      </concept>
      <concept>
        <code value="OMIM:606053" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:606054" />
        <display value="PROPIONIC ACIDEMIA" />
      </concept>
      <concept>
        <code value="OMIM:606056" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIb" />
      </concept>
      <concept>
        <code value="OMIM:606068" />
        <display value="RETINITIS PIGMENTOSA 28" />
      </concept>
      <concept>
        <code value="OMIM:606069" />
        <display value="HEMOCHROMATOSIS, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:606070" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 21" />
      </concept>
      <concept>
        <code value="OMIM:606071" />
        <display value="HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC" />
      </concept>
      <concept>
        <code value="OMIM:606072" />
        <display value="RIPPLING MUSCLE DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:606082" />
        <display value="GOITER, MULTINODULAR 3" />
      </concept>
      <concept>
        <code value="OMIM:606129" />
        <display value="DIAMOND-BLACKFAN ANEMIA 2" />
      </concept>
      <concept>
        <code value="OMIM:606156" />
        <display value="SENER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606159" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3" />
      </concept>
      <concept>
        <code value="OMIM:606164" />
        <display value="DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:606170" />
        <display value="GENITOPATELLAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606174" />
        <display value="BACULUM, CONGENITAL ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:606175" />
        <display value="CARNITINE ACETYLTRANSFERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:606176" />
        <display value="DIABETES MELLITUS, PERMANENT NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:606177" />
        <display value="PARS PLANITIS" />
      </concept>
      <concept>
        <code value="OMIM:606179" />
        <display value="ANEURYSMAL BONE CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:606183" />
        <display value="LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:606187" />
        <display value="ALZHEIMER DISEASE 7" />
      </concept>
      <concept>
        <code value="OMIM:606190" />
        <display value="MENINGIOMA, RADIATION-INDUCED" />
      </concept>
      <concept>
        <code value="OMIM:606215" />
        <display value="ATRIOVENTRICULAR SEPTAL DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:606217" />
        <display value="ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:606220" />
        <display value="MENTAL RETARDATION, SHORT STATURE, FACIAL ANOMALIES, AND JOINT DISLOCATIONS" />
      </concept>
      <concept>
        <code value="OMIM:606232" />
        <display value="PHELAN-MCDERMID SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606240" />
        <display value="THYROID CANCER, NONMEDULLARY, 3" />
      </concept>
      <concept>
        <code value="OMIM:606242" />
        <display value="MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES, AND FACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:606243" />
        <display value="ALVEOLAR SOFT PART SARCOMA" />
      </concept>
      <concept>
        <code value="OMIM:606255" />
        <display value="STATURE AS A QUANTITATIVE TRAIT" />
      </concept>
      <concept>
        <code value="OMIM:606256" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:606257" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:606258" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:606263" />
        <display value="PAGET DISEASE OF BONE 4" />
      </concept>
      <concept>
        <code value="OMIM:606282" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 24" />
      </concept>
      <concept>
        <code value="OMIM:606324" />
        <display value="PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:606325" />
        <display value="HETEROTAXY, VISCERAL, 3, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:606346" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 22" />
      </concept>
      <concept>
        <code value="OMIM:606348" />
        <display value="INFLAMMATORY BOWEL DISEASE 5" />
      </concept>
      <concept>
        <code value="OMIM:606349" />
        <display value="GAMBLING, PATHOLOGIC" />
      </concept>
      <concept>
        <code value="OMIM:606353" />
        <display value="PRIMARY LATERAL SCLEROSIS, JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:606367" />
        <display value="IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY" />
      </concept>
      <concept>
        <code value="OMIM:606369" />
        <display value="MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:606391" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG" />
      </concept>
      <concept>
        <code value="OMIM:606392" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:606394" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:606407" />
        <display value="HYPOTONIA-CYSTINURIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606408" />
        <display value="EHLERS-DANLOS SYNDROME, CLASSIC-LIKE" />
      </concept>
      <concept>
        <code value="OMIM:606438" />
        <display value="HUNTINGTON DISEASE-LIKE 2" />
      </concept>
      <concept>
        <code value="OMIM:606445" />
        <display value="PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:606451" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 30" />
      </concept>
      <concept>
        <code value="OMIM:606460" />
        <display value="LONGEVITY 2" />
      </concept>
      <concept>
        <code value="OMIM:606482" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B" />
      </concept>
      <concept>
        <code value="OMIM:606483" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A" />
      </concept>
      <concept>
        <code value="OMIM:606519" />
        <display value="PHACE ASSOCIATION" />
      </concept>
      <concept>
        <code value="OMIM:606527" />
        <display value="MEGARBANE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606528" />
        <display value="HOMOZYGOUS 11p15-p14 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606529" />
        <display value="CRANIOSYNOSTOSIS SYNDROME, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:606545" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:606552" />
        <display value="EPISODIC ATAXIA, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:606554" />
        <display value="EPISODIC ATAXIA, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:606574" />
        <display value="ALBINISM, OCULOCUTANEOUS, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:606579" />
        <display value="VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1" />
      </concept>
      <concept>
        <code value="OMIM:606581" />
        <display value="POLYSUBSTANCE ABUSE, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:606593" />
        <display value="LIG4 SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606595" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F" />
      </concept>
      <concept>
        <code value="OMIM:606612" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5" />
      </concept>
      <concept>
        <code value="OMIM:606613" />
        <display value="HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:606616" />
        <display value="DYSLEXIA, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:606631" />
        <display value="CAMURATI-ENGELMANN DISEASE, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:606632" />
        <display value="ODOR, MALE, WOMEN'S CHOICE OF" />
      </concept>
      <concept>
        <code value="OMIM:606640" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 3" />
      </concept>
      <concept>
        <code value="OMIM:606641" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:606643" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:606656" />
        <display value="BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:606657" />
        <display value="GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:606658" />
        <display value="SPINOCEREBELLAR ATAXIA 15" />
      </concept>
      <concept>
        <code value="OMIM:606660" />
        <display value="MELANOMA, UVEAL, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:606661" />
        <display value="MELANOMA, UVEAL, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:606662" />
        <display value="WAARDENBURG SYNDROME, TYPE 2C" />
      </concept>
      <concept>
        <code value="OMIM:606664" />
        <display value="GLYCINE N-METHYLTRANSFERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:606668" />
        <display value="INFLAMMATORY BOWEL DISEASE 8" />
      </concept>
      <concept>
        <code value="OMIM:606674" />
        <display value="INFLAMMATORY BOWEL DISEASE 6" />
      </concept>
      <concept>
        <code value="OMIM:606675" />
        <display value="INFLAMMATORY BOWEL DISEASE 4" />
      </concept>
      <concept>
        <code value="OMIM:606685" />
        <display value="CARDIOMYOPATHY, DILATED, 1L" />
      </concept>
      <concept>
        <code value="OMIM:606688" />
        <display value="SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:606689" />
        <display value="GLAUCOMA 1, OPEN ANGLE, B" />
      </concept>
      <concept>
        <code value="OMIM:606690" />
        <display value="LYMPHANGIOLEIOMYOMATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:606693" />
        <display value="KUFOR-RAKEB SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606703" />
        <display value="DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA" />
      </concept>
      <concept>
        <code value="OMIM:606705" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 36" />
      </concept>
      <concept>
        <code value="OMIM:606708" />
        <display value="SPLIT-HAND/FOOT MALFORMATION 5" />
      </concept>
      <concept>
        <code value="OMIM:606711" />
        <display value="SPECIFIC LANGUAGE IMPAIRMENT 1" />
      </concept>
      <concept>
        <code value="OMIM:606712" />
        <display value="SPECIFIC LANGUAGE IMPAIRMENT 2" />
      </concept>
      <concept>
        <code value="OMIM:606713" />
        <display value="VAN DER WOUDE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:606719" />
        <display value="MELANOMA-PANCREATIC CANCER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606721" />
        <display value="PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606744" />
        <display value="SECKEL SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:606752" />
        <display value="ACUTE HEMORRHAGIC LEUKOENCEPHALITIS" />
      </concept>
      <concept>
        <code value="OMIM:606762" />
        <display value="HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:606763" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:606764" />
        <display value="GASTROINTESTINAL STROMAL TUMOR" />
      </concept>
      <concept>
        <code value="OMIM:606766" />
        <display value="SPERMATOGENIC FAILURE 3" />
      </concept>
      <concept>
        <code value="OMIM:606768" />
        <display value="MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET" />
      </concept>
      <concept>
        <code value="OMIM:606770" />
        <display value="ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:606771" />
        <display value="ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:606772" />
        <display value="MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKIN ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:606773" />
        <display value="HEMIFACIAL MYOHYPERPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:606777" />
        <display value="GLUT1 DEFICIENCY SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:606785" />
        <display value="CRIGLER-NAJJAR SYNDROME, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:606787" />
        <display value="PERIPHERAL ARTERIAL OCCLUSIVE DISEASE 1" />
      </concept>
      <concept>
        <code value="OMIM:606788" />
        <display value="ANOREXIA NERVOSA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:606789" />
        <display value="FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:606798" />
        <display value="BLEPHAROSPASM, BENIGN ESSENTIAL, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:606799" />
        <display value="STROKE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:606812" />
        <display value="FUMARASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:606824" />
        <display value="GLUCOSE/GALACTOSE MALABSORPTION" />
      </concept>
      <concept>
        <code value="OMIM:606835" />
        <display value="DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:606840" />
        <display value="PARASOMNIA, SLEEP BRUXISM TYPE" />
      </concept>
      <concept>
        <code value="OMIM:606842" />
        <display value="CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS" />
      </concept>
      <concept>
        <code value="OMIM:606843" />
        <display value="IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:606851" />
        <display value="CREE MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:606852" />
        <display value="PARKINSON DISEASE 10" />
      </concept>
      <concept>
        <code value="OMIM:606854" />
        <display value="POLYMICROGYRIA, BILATERAL FRONTOPARIETAL" />
      </concept>
      <concept>
        <code value="OMIM:606856" />
        <display value="PANCREATIC CANCER, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:606864" />
        <display value="PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA" />
      </concept>
      <concept>
        <code value="OMIM:606874" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:606875" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:606889" />
        <display value="ALZHEIMER DISEASE 4" />
      </concept>
      <concept>
        <code value="OMIM:606893" />
        <display value="VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS" />
      </concept>
      <concept>
        <code value="OMIM:606894" />
        <display value="DUODENOJEJUNAL ATRESIA WITH VOLVULUS, ABSENT DORSAL MESENTERY, AND ABSENT SUPERIOR MESENTERIC ARTERY" />
      </concept>
      <concept>
        <code value="OMIM:606895" />
        <display value="SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWED ZYGOMATIC ARCH" />
      </concept>
      <concept>
        <code value="OMIM:606896" />
        <display value="DYSLEXIA, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:606928" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:606943" />
        <display value="USHER SYNDROME, TYPE IG" />
      </concept>
      <concept>
        <code value="OMIM:606952" />
        <display value="ALBINISM, OCULOCUTANEOUS, TYPE IB" />
      </concept>
      <concept>
        <code value="OMIM:606960" />
        <display value="INSULINOMA TUMOR SUPPRESSOR GENE LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:606963" />
        <display value="PULMONARY DISEASE, CHRONIC OBSTRUCTIVE" />
      </concept>
      <concept>
        <code value="OMIM:606966" />
        <display value="NEPHRONOPHTHISIS 4" />
      </concept>
      <concept>
        <code value="OMIM:606972" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:606984" />
        <display value="HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:606995" />
        <display value="SENIOR-LOKEN SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:606996" />
        <display value="SENIOR-LOKEN SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:607004" />
        <display value="BRACHYDACTYLY, TYPE A1, B" />
      </concept>
      <concept>
        <code value="OMIM:607014" />
        <display value="HURLER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607015" />
        <display value="HURLER-SCHEIE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607016" />
        <display value="SCHEIE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607017" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 21" />
      </concept>
      <concept>
        <code value="OMIM:607039" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 22" />
      </concept>
      <concept>
        <code value="OMIM:607044" />
        <display value="T-BOX 24" />
      </concept>
      <concept>
        <code value="OMIM:607053" />
        <display value="HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:607060" />
        <display value="PARKINSON DISEASE 8, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:607078" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, 5" />
      </concept>
      <concept>
        <code value="OMIM:607080" />
        <display value="46,XY GONADAL DYSGENESIS, PARTIAL, WITH MINIFASCICULAR NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:607084" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 31" />
      </concept>
      <concept>
        <code value="OMIM:607085" />
        <display value="MYASTHENIA GRAVIS WITH THYMUS HYPERPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:607086" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 1" />
      </concept>
      <concept>
        <code value="OMIM:607087" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 2" />
      </concept>
      <concept>
        <code value="OMIM:607088" />
        <display value="SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3" />
      </concept>
      <concept>
        <code value="OMIM:607091" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IId" />
      </concept>
      <concept>
        <code value="OMIM:607095" />
        <display value="ANAUXETIC DYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:607101" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 30" />
      </concept>
      <concept>
        <code value="OMIM:607107" />
        <display value="NASOPHARYNGEAL CARCINOMA" />
      </concept>
      <concept>
        <code value="OMIM:607115" />
        <display value="CINCA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607116" />
        <display value="ALZHEIMER DISEASE 8" />
      </concept>
      <concept>
        <code value="OMIM:607131" />
        <display value="AL-GAZALI-BAKALINOVA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607132" />
        <display value="LARYNGEAL ATRESIA, ENCEPHALOCELE, AND LIMB DEFORMITIES" />
      </concept>
      <concept>
        <code value="OMIM:607134" />
        <display value="SPECIFIC LANGUAGE IMPAIRMENT 3" />
      </concept>
      <concept>
        <code value="OMIM:607135" />
        <display value="CREATININE CLEARANCE QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:607136" />
        <display value="SPINOCEREBELLAR ATAXIA 17" />
      </concept>
      <concept>
        <code value="OMIM:607140" />
        <display value="ANGIOID STREAKS" />
      </concept>
      <concept>
        <code value="OMIM:607143" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig" />
      </concept>
      <concept>
        <code value="OMIM:607151" />
        <display value="MOYAMOYA DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:607152" />
        <display value="SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:607154" />
        <display value="ALLERGIC RHINITIS" />
      </concept>
      <concept>
        <code value="OMIM:607155" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5" />
      </concept>
      <concept>
        <code value="OMIM:607161" />
        <display value="MULTIPLE CONGENITAL ANOMALIES SYNDROME WITH CLOVERLEAF SKULL" />
      </concept>
      <concept>
        <code value="OMIM:607174" />
        <display value="MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:607196" />
        <display value="MICROCEPHALY, AMISH TYPE" />
      </concept>
      <concept>
        <code value="OMIM:607197" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:607200" />
        <display value="THYROID DYSHORMONOGENESIS 6" />
      </concept>
      <concept>
        <code value="OMIM:607202" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:607208" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6" />
      </concept>
      <concept>
        <code value="OMIM:607214" />
        <display value="ANONYCHIA, TOTAL, WITH MICROCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:607221" />
        <display value="EPILEPSY, PARTIAL, WITH PERICENTRAL SPIKES" />
      </concept>
      <concept>
        <code value="OMIM:607225" />
        <display value="SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING" />
      </concept>
      <concept>
        <code value="OMIM:607236" />
        <display value="HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA, AND PALLIDAL DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:607239" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 33" />
      </concept>
      <concept>
        <code value="OMIM:607248" />
        <display value="GLIOMA SUSCEPTIBILITY 4" />
      </concept>
      <concept>
        <code value="OMIM:607250" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:607258" />
        <display value="HYPERCALCIURIA, ABSORPTIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:607259" />
        <display value="SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:607271" />
        <display value="CASPASE 8 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:607276" />
        <display value="RESTING HEART RATE, VARIATION IN" />
      </concept>
      <concept>
        <code value="OMIM:607277" />
        <display value="ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:607278" />
        <display value="OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:607279" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:607304" />
        <display value="CATARACT 27" />
      </concept>
      <concept>
        <code value="OMIM:607308" />
        <display value="MAMMOGRAPHIC DENSITY" />
      </concept>
      <concept>
        <code value="OMIM:607313" />
        <display value="GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1" />
      </concept>
      <concept>
        <code value="OMIM:607317" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4" />
      </concept>
      <concept>
        <code value="OMIM:607323" />
        <display value="DUANE-RADIAL RAY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607324" />
        <display value="POLYDACTYLY, POSTAXIAL, TYPE A3" />
      </concept>
      <concept>
        <code value="OMIM:607326" />
        <display value="SMITH-MCCORT DYSPLASIA 1" />
      </concept>
      <concept>
        <code value="OMIM:607329" />
        <display value="HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:607330" />
        <display value="LATHOSTEROLOSIS" />
      </concept>
      <concept>
        <code value="OMIM:607339" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:607341" />
        <display value="FOCAL CORTICAL DYSPLASIA, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:607346" />
        <display value="SPINOCEREBELLAR ATAXIA 19" />
      </concept>
      <concept>
        <code value="OMIM:607354" />
        <display value="SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:607361" />
        <display value="MECKEL SYNDROME, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:607364" />
        <display value="BARTTER SYNDROME, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:607371" />
        <display value="DYSTONIA, JUVENILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:607373" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:607395" />
        <display value="STREPTOCOCCUS, GROUP A, SEVERITY OF INFECTION BY" />
      </concept>
      <concept>
        <code value="OMIM:607398" />
        <display value="GLUCOCORTICOID DEFICIENCY 2" />
      </concept>
      <concept>
        <code value="OMIM:607411" />
        <display value="PATENT DUCTUS ARTERIOSUS 1" />
      </concept>
      <concept>
        <code value="OMIM:607413" />
        <display value="ALZHEIMER DISEASE NEURONAL THREAD PROTEIN" />
      </concept>
      <concept>
        <code value="OMIM:607417" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:607426" />
        <display value="COENZYME Q10 DEFICIENCY, PRIMARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:607432" />
        <display value="LISSENCEPHALY 1" />
      </concept>
      <concept>
        <code value="OMIM:607446" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:607447" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:607450" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8" />
      </concept>
      <concept>
        <code value="OMIM:607453" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 44" />
      </concept>
      <concept>
        <code value="OMIM:607454" />
        <display value="SPINOCEREBELLAR ATAXIA 21" />
      </concept>
      <concept>
        <code value="OMIM:607457" />
        <display value="GIL BLOOD GROUP" />
      </concept>
      <concept>
        <code value="OMIM:607458" />
        <display value="SPINOCEREBELLAR ATAXIA 18" />
      </concept>
      <concept>
        <code value="OMIM:607459" />
        <display value="SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS" />
      </concept>
      <concept>
        <code value="OMIM:607464" />
        <display value="THYROID CARCINOMA, HURTHLE CELL" />
      </concept>
      <concept>
        <code value="OMIM:607473" />
        <display value="VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2" />
      </concept>
      <concept>
        <code value="OMIM:607475" />
        <display value="BOTHNIA RETINAL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:607476" />
        <display value="NEWFOUNDLAND ROD-CONE DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:607482" />
        <display value="CARDIOMYOPATHY, DILATED, 1M" />
      </concept>
      <concept>
        <code value="OMIM:607483" />
        <display value="THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:607485" />
        <display value="FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:607486" />
        <display value="KNOPS BLOOD GROUP SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:607487" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25" />
      </concept>
      <concept>
        <code value="OMIM:607488" />
        <display value="DYSTONIA 15, MYOCLONIC" />
      </concept>
      <concept>
        <code value="OMIM:607498" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:607499" />
        <display value="BULIMIA NERVOSA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:607501" />
        <display value="MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:607504" />
        <display value="HEADACHE ASSOCIATED WITH SEXUAL ACTIVITY" />
      </concept>
      <concept>
        <code value="OMIM:607507" />
        <display value="PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:607508" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:607514" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10" />
      </concept>
      <concept>
        <code value="OMIM:607516" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:607523" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 8" />
      </concept>
      <concept>
        <code value="OMIM:607539" />
        <display value="CAMPTOSYNPOLYDACTYLY, COMPLEX" />
      </concept>
      <concept>
        <code value="OMIM:607540" />
        <display value="SECRETORY DIARRHEA, MYOPATHY, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:607541" />
        <display value="CORNEAL DYSTROPHY, AVELLINO TYPE" />
      </concept>
      <concept>
        <code value="OMIM:607543" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA WITH BOWED FOREARMS AND FACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:607554" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:607565" />
        <display value="SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:607569" />
        <display value="MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:607572" />
        <display value="LEPROSY, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:607578" />
        <display value="BREATH-HOLDING SPELLS" />
      </concept>
      <concept>
        <code value="OMIM:607584" />
        <display value="SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:607592" />
        <display value="PROSTATE CANCER AGGRESSIVENESS QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 19" />
      </concept>
      <concept>
        <code value="OMIM:607594" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 1" />
      </concept>
      <concept>
        <code value="OMIM:607595" />
        <display value="BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:607596" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 1A" />
      </concept>
      <concept>
        <code value="OMIM:607597" />
        <display value="MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:607598" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:607600" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX SUPERFICIALIS" />
      </concept>
      <concept>
        <code value="OMIM:607602" />
        <display value="ICHTHYOSIS, CYCLIC, WITH EPIDERMOLYTIC HYPERKERATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:607616" />
        <display value="NIEMANN-PICK DISEASE, TYPE B" />
      </concept>
      <concept>
        <code value="OMIM:607624" />
        <display value="GRISCELLI SYNDROME, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:607625" />
        <display value="NIEMANN-PICK DISEASE, TYPE C2" />
      </concept>
      <concept>
        <code value="OMIM:607626" />
        <display value="ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS" />
      </concept>
      <concept>
        <code value="OMIM:607628" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11" />
      </concept>
      <concept>
        <code value="OMIM:607631" />
        <display value="EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:607634" />
        <display value="OSTEOPETROSIS, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:607636" />
        <display value="VAN BUCHEM DISEASE, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:607641" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB" />
      </concept>
      <concept>
        <code value="OMIM:607644" />
        <display value="CANDIDIASIS, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:607654" />
        <display value="KERATOSIS PALMOPLANTARIS STRIATA III" />
      </concept>
      <concept>
        <code value="OMIM:607655" />
        <display value="SKIN FRAGILITY-WOOLLY HAIR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607656" />
        <display value="CURLY HAIR-ACRAL KERATODERMA-CARIES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607658" />
        <display value="HYPOTRICHOSIS-OSTEOLYSIS-PERIODONTITIS-PALMOPLANTAR KERATODERMA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607665" />
        <display value="TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS" />
      </concept>
      <concept>
        <code value="OMIM:607671" />
        <display value="DYSTONIA 13, TORSION, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:607674" />
        <display value="CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:607676" />
        <display value="IRAK4 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:607677" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I" />
      </concept>
      <concept>
        <code value="OMIM:607678" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D" />
      </concept>
      <concept>
        <code value="OMIM:607681" />
        <display value="EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:607682" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:607683" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 52" />
      </concept>
      <concept>
        <code value="OMIM:607684" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E" />
      </concept>
      <concept>
        <code value="OMIM:607685" />
        <display value="HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC" />
      </concept>
      <concept>
        <code value="OMIM:607687" />
        <display value="HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:607688" />
        <display value="PARKINSON DISEASE 11, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:607694" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:607706" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:607721" />
        <display value="NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1" />
      </concept>
      <concept>
        <code value="OMIM:607728" />
        <display value="POROKERATOSIS 4, DISSEMINATED SUPERFICIAL ACTINIC TYPE" />
      </concept>
      <concept>
        <code value="OMIM:607731" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H" />
      </concept>
      <concept>
        <code value="OMIM:607734" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F" />
      </concept>
      <concept>
        <code value="OMIM:607736" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J" />
      </concept>
      <concept>
        <code value="OMIM:607745" />
        <display value="SEIZURES, BENIGN FAMILIAL INFANTILE, 3" />
      </concept>
      <concept>
        <code value="OMIM:607748" />
        <display value="HYPERCHOLANEMIA, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:607765" />
        <display value="BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:607778" />
        <display value="ACROCAPITOFEMORAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:607785" />
        <display value="JUVENILE MYELOMONOCYTIC LEUKEMIA" />
      </concept>
      <concept>
        <code value="OMIM:607791" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D" />
      </concept>
      <concept>
        <code value="OMIM:607812" />
        <display value="CRANIOLENTICULOSUTURAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:607821" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 37" />
      </concept>
      <concept>
        <code value="OMIM:607822" />
        <display value="ALZHEIMER DISEASE 3" />
      </concept>
      <concept>
        <code value="OMIM:607823" />
        <display value="HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607829" />
        <display value="MITRAL VALVE PROLAPSE 2" />
      </concept>
      <concept>
        <code value="OMIM:607831" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K" />
      </concept>
      <concept>
        <code value="OMIM:607832" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:607834" />
        <display value="ANXIETY" />
      </concept>
      <concept>
        <code value="OMIM:607836" />
        <display value="AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:607841" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 48" />
      </concept>
      <concept>
        <code value="OMIM:607842" />
        <display value="AURAL ATRESIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:607847" />
        <display value="NEUTROPENIA, NONIMMUNE CHRONIC IDIOPATHIC, OF ADULTS" />
      </concept>
      <concept>
        <code value="OMIM:607850" />
        <display value="OSTEOARTHRITIS SUSCEPTIBILITY 3" />
      </concept>
      <concept>
        <code value="OMIM:607853" />
        <display value="PANIC DISORDER 2" />
      </concept>
      <concept>
        <code value="OMIM:607855" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A" />
      </concept>
      <concept>
        <code value="OMIM:607857" />
        <display value="PSORIASIS 9, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:607859" />
        <display value="ANGIOMA, TUFTED" />
      </concept>
      <concept>
        <code value="OMIM:607864" />
        <display value="CAUDAL DUPLICATION ANOMALY" />
      </concept>
      <concept>
        <code value="OMIM:607872" />
        <display value="CHROMOSOME 1p36 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:607876" />
        <display value="EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:607893" />
        <display value="OVARIAN CANCER, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:607903" />
        <display value="HYPOTRICHOSIS 6" />
      </concept>
      <concept>
        <code value="OMIM:607906" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii" />
      </concept>
      <concept>
        <code value="OMIM:607907" />
        <display value="DERMATOFIBROSARCOMA PROTUBERANS" />
      </concept>
      <concept>
        <code value="OMIM:607921" />
        <display value="RETINITIS PIGMENTOSA 30" />
      </concept>
      <concept>
        <code value="OMIM:607932" />
        <display value="MICROPHTHALMIA, SYNDROMIC 6" />
      </concept>
      <concept>
        <code value="OMIM:607936" />
        <display value="PEELING SKIN SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:607941" />
        <display value="ATRIAL SEPTAL DEFECT 2" />
      </concept>
      <concept>
        <code value="OMIM:607944" />
        <display value="SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION" />
      </concept>
      <concept>
        <code value="OMIM:607948" />
        <display value="MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:607949" />
        <display value="MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:607965" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:607966" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:607967" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608013" />
        <display value="GAUCHER DISEASE, PERINATAL LETHAL" />
      </concept>
      <concept>
        <code value="OMIM:608022" />
        <display value="DIAPHANOSPONDYLODYSOSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:608026" />
        <display value="HYPERTENSIVE NEPHROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:608027" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:608028" />
        <display value="THAI SYMPHALANGISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608029" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6" />
      </concept>
      <concept>
        <code value="OMIM:608030" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 6 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:608031" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 7" />
      </concept>
      <concept>
        <code value="OMIM:608033" />
        <display value="ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608035" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:608036" />
        <display value="DIABETES MELLITUS, NONINSULIN-DEPENDENT, 4" />
      </concept>
      <concept>
        <code value="OMIM:608045" />
        <display value="REPRESSOR OF TELOMERASE EXPRESSION 1" />
      </concept>
      <concept>
        <code value="OMIM:608049" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608051" />
        <display value="MACULAR DYSTROPHY, RETINAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:608063" />
        <display value="BILE AND PANCREATIC DUCTS, COMPLETE ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:608068" />
        <display value="NEUTROPHILIC DERMATOSIS, ACUTE FEBRILE" />
      </concept>
      <concept>
        <code value="OMIM:608078" />
        <display value="SCHIZOPHRENIA 11" />
      </concept>
      <concept>
        <code value="OMIM:608088" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH AND GASTROESOPHAGEAL REFLUX" />
      </concept>
      <concept>
        <code value="OMIM:608089" />
        <display value="ENDOMETRIAL CANCER" />
      </concept>
      <concept>
        <code value="OMIM:608091" />
        <display value="JOUBERT SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:608093" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij" />
      </concept>
      <concept>
        <code value="OMIM:608096" />
        <display value="EPILEPSY, FAMILIAL TEMPORAL LOBE, 2" />
      </concept>
      <concept>
        <code value="OMIM:608097" />
        <display value="PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:608098" />
        <display value="PERIVENTRICULAR NODULAR HETEROTOPIA 3" />
      </concept>
      <concept>
        <code value="OMIM:608099" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:608104" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih" />
      </concept>
      <concept>
        <code value="OMIM:608105" />
        <display value="EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA AND WRITER'S CRAMP" />
      </concept>
      <concept>
        <code value="OMIM:608106" />
        <display value="IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:608115" />
        <display value="OVARIAN HYPERSTIMULATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608118" />
        <display value="ZINC DEFICIENCY, TRANSIENT NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:608133" />
        <display value="RETINITIS PIGMENTOSA 7" />
      </concept>
      <concept>
        <code value="OMIM:608149" />
        <display value="KAGAMI-OGATA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608154" />
        <display value="LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES" />
      </concept>
      <concept>
        <code value="OMIM:608156" />
        <display value="NABLUS MASK-LIKE FACIAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608158" />
        <display value="CoQ-RESPONSIVE OXPHOS DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608161" />
        <display value="MACULAR DYSTROPHY, VITELLIFORM, 3" />
      </concept>
      <concept>
        <code value="OMIM:608173" />
        <display value="AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:608174" />
        <display value="AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:608175" />
        <display value="AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608176" />
        <display value="AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:608180" />
        <display value="SYNPOLYDACTYLY 2" />
      </concept>
      <concept>
        <code value="OMIM:608184" />
        <display value="IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:608189" />
        <display value="TROPICAL CALCIFIC PANCREATITIS" />
      </concept>
      <concept>
        <code value="OMIM:608194" />
        <display value="CONE-ROD DYSTROPHY 13" />
      </concept>
      <concept>
        <code value="OMIM:608203" />
        <display value="NEUTROPHIL IMMUNODEFICIENCY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608207" />
        <display value="KALA-AZAR, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:608217" />
        <display value="SEIZURES, BENIGN FAMILIAL NEONATAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:608219" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 38" />
      </concept>
      <concept>
        <code value="OMIM:608220" />
        <display value="SPASTIC PARAPLEGIA 25, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:608223" />
        <display value="ASPIRIN RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:608224" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 41" />
      </concept>
      <concept>
        <code value="OMIM:608227" />
        <display value="CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRAL NEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:608232" />
        <display value="LEUKEMIA, CHRONIC MYELOID" />
      </concept>
      <concept>
        <code value="OMIM:608233" />
        <display value="HERMANSKY-PUDLAK SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:608236" />
        <display value="SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:608244" />
        <display value="OTOSCLEROSIS 3" />
      </concept>
      <concept>
        <code value="OMIM:608251" />
        <display value="PHOBIA, SPECIFIC" />
      </concept>
      <concept>
        <code value="OMIM:608257" />
        <display value="MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:608264" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 40" />
      </concept>
      <concept>
        <code value="OMIM:608265" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 39" />
      </concept>
      <concept>
        <code value="OMIM:608266" />
        <display value="PARATHYROID CARCINOMA" />
      </concept>
      <concept>
        <code value="OMIM:608278" />
        <display value="GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGE JOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLAR ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:608279" />
        <display value="CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:608281" />
        <display value="SCIMITAR ANOMALY, MULTIPLE CARDIAC MALFORMATIONS, AND CRANIOFACIAL AND CENTRAL NERVOUS SYSTEM ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:608290" />
        <display value="LELIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608307" />
        <display value="CARBAMOYL PHOSPHATE SYNTHETASE I" />
      </concept>
      <concept>
        <code value="OMIM:608316" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:608318" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:608320" />
        <display value="CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1" />
      </concept>
      <concept>
        <code value="OMIM:608323" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C" />
      </concept>
      <concept>
        <code value="OMIM:608328" />
        <display value="WEILL-MARCHESANI SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:608340" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A" />
      </concept>
      <concept>
        <code value="OMIM:608345" />
        <display value="NYSTAGMUS 3, CONGENITAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:608354" />
        <display value="CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 1" />
      </concept>
      <concept>
        <code value="OMIM:608355" />
        <display value="PARKES WEBER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608358" />
        <display value="MYOPATHY, MYOSIN STORAGE, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:608361" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:608363" />
        <display value="CHROMOSOME 22q11.2 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608367" />
        <display value="MYOPIA 17, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:608371" />
        <display value="OROFACIAL CLEFT 4" />
      </concept>
      <concept>
        <code value="OMIM:608372" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 49" />
      </concept>
      <concept>
        <code value="OMIM:608380" />
        <display value="RETINITIS PIGMENTOSA 26" />
      </concept>
      <concept>
        <code value="OMIM:608389" />
        <display value="BRANCHIOOTIC SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:608390" />
        <display value="MYOTONIA, POTASSIUM-AGGRAVATED" />
      </concept>
      <concept>
        <code value="OMIM:608391" />
        <display value="AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:608392" />
        <display value="AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608393" />
        <display value="MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:608394" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 43" />
      </concept>
      <concept>
        <code value="OMIM:608404" />
        <display value="PLATELET GLYCOPROTEIN IV DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608406" />
        <display value="VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608410" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7" />
      </concept>
      <concept>
        <code value="OMIM:608415" />
        <display value="PROLONGED ELECTRORETINAL RESPONSE SUPPRESSION" />
      </concept>
      <concept>
        <code value="OMIM:608423" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:608432" />
        <display value="CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:608437" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:608443" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:608445" />
        <display value="SPEECH-SOUND DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:608446" />
        <display value="MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:608447" />
        <display value="CAROTID INTIMAL MEDIAL THICKNESS 2" />
      </concept>
      <concept>
        <code value="OMIM:608448" />
        <display value="INFLAMMATORY BOWEL DISEASE 9" />
      </concept>
      <concept>
        <code value="OMIM:608456" />
        <display value="FAMILIAL ADENOMATOUS POLYPOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:608462" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:608470" />
        <display value="CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:608471" />
        <display value="CORNEAL DYSTROPHY, LATTICE TYPE IIIA" />
      </concept>
      <concept>
        <code value="OMIM:608474" />
        <display value="MYOPIA 5, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:608484" />
        <display value="CONGENITAL CORNEAL OPACITIES, CORNEA GUTTATA, AND CORECTOPIA" />
      </concept>
      <concept>
        <code value="OMIM:608509" />
        <display value="ALOPECIA UNIVERSALIS CONGENITA, XY GONADAL DYSGENESIS, AND LARYNGOMALACIA" />
      </concept>
      <concept>
        <code value="OMIM:608516" />
        <display value="MAJOR DEPRESSIVE DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:608518" />
        <display value="OROFACIODIGITAL SYNDROME VII" />
      </concept>
      <concept>
        <code value="OMIM:608520" />
        <display value="MAJOR DEPRESSIVE DISORDER 1" />
      </concept>
      <concept>
        <code value="OMIM:608526" />
        <display value="PERIODONTITIS, AGGRESSIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:608540" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik" />
      </concept>
      <concept>
        <code value="OMIM:608542" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 2" />
      </concept>
      <concept>
        <code value="OMIM:608543" />
        <display value="SCHIZOPHRENIA 12" />
      </concept>
      <concept>
        <code value="OMIM:608545" />
        <display value="LARSEN-LIKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608553" />
        <display value="LEBER CONGENITAL AMAUROSIS 9" />
      </concept>
      <concept>
        <code value="OMIM:608556" />
        <display value="LEGIONNAIRE DISEASE, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:608557" />
        <display value="MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:608558" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:608559" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 6" />
      </concept>
      <concept>
        <code value="OMIM:608562" />
        <display value="POLYDACTYLY, POSTAXIAL, TYPE A4" />
      </concept>
      <concept>
        <code value="OMIM:608565" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 35" />
      </concept>
      <concept>
        <code value="OMIM:608567" />
        <display value="SICK SINUS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:608569" />
        <display value="CARDIOMYOPATHY, DILATED, 1O" />
      </concept>
      <concept>
        <code value="OMIM:608571" />
        <display value="ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:608572" />
        <display value="BURN-MCKEOWN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608579" />
        <display value="SEVERE CUTANEOUS ADVERSE REACTION, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:608580" />
        <display value="MYOSIN, HEAVY CHAIN 16, SKELETAL MUSCLE, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:608583" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:608584" />
        <display value="ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:608585" />
        <display value="BRACHIAL PALSY, FAMILIAL CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:608586" />
        <display value="KERATOCONUS 3" />
      </concept>
      <concept>
        <code value="OMIM:608594" />
        <display value="LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:608600" />
        <display value="LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1" />
      </concept>
      <concept>
        <code value="OMIM:608611" />
        <display value="RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608612" />
        <display value="MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:608615" />
        <display value="OLIGODONTIA-COLORECTAL CANCER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608622" />
        <display value="HYPERTENSION, DIASTOLIC, RESISTANCE TO" />
      </concept>
      <concept>
        <code value="OMIM:608624" />
        <display value="MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA" />
      </concept>
      <concept>
        <code value="OMIM:608627" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 8" />
      </concept>
      <concept>
        <code value="OMIM:608629" />
        <display value="JOUBERT SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:608631" />
        <display value="ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:608634" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB" />
      </concept>
      <concept>
        <code value="OMIM:608636" />
        <display value="CHROMOSOME 15q11-q13 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608638" />
        <display value="ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:608641" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 28" />
      </concept>
      <concept>
        <code value="OMIM:608643" />
        <display value="AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608644" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 3" />
      </concept>
      <concept>
        <code value="OMIM:608645" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 31" />
      </concept>
      <concept>
        <code value="OMIM:608646" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 4" />
      </concept>
      <concept>
        <code value="OMIM:608647" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 5" />
      </concept>
      <concept>
        <code value="OMIM:608649" />
        <display value="ICHTHYOSIS PREMATURITY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608652" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 47" />
      </concept>
      <concept>
        <code value="OMIM:608653" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 32, WITH OR WITHOUT IMMOTILE SPERM" />
      </concept>
      <concept>
        <code value="OMIM:608654" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:608656" />
        <display value="PROSTATE CANCER, HEREDITARY, 3" />
      </concept>
      <concept>
        <code value="OMIM:608658" />
        <display value="PROSTATE CANCER, HEREDITARY, 4" />
      </concept>
      <concept>
        <code value="OMIM:608670" />
        <display value="ROBIN SEQUENCE WITH DISTINCTIVE FACIAL APPEARANCE AND BRACHYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:608673" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L" />
      </concept>
      <concept>
        <code value="OMIM:608681" />
        <display value="SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:608687" />
        <display value="SPINOCEREBELLAR ATAXIA 20" />
      </concept>
      <concept>
        <code value="OMIM:608688" />
        <display value="AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608691" />
        <display value="MAJOR DEPRESSIVE DISORDER 2" />
      </concept>
      <concept>
        <code value="OMIM:608695" />
        <display value="GLAUCOMA 1, OPEN ANGLE, J" />
      </concept>
      <concept>
        <code value="OMIM:608696" />
        <display value="GLAUCOMA 1, OPEN ANGLE, K" />
      </concept>
      <concept>
        <code value="OMIM:608703" />
        <display value="SPINOCEREBELLAR ATAXIA 25" />
      </concept>
      <concept>
        <code value="OMIM:608709" />
        <display value="LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:608710" />
        <display value="GRANULOMATOSIS WITH POLYANGIITIS" />
      </concept>
      <concept>
        <code value="OMIM:608716" />
        <display value="MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:608720" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:608728" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED" />
      </concept>
      <concept>
        <code value="OMIM:608742" />
        <display value="HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:608747" />
        <display value="INSULIN-LIKE GROWTH FACTOR I DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608751" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8" />
      </concept>
      <concept>
        <code value="OMIM:608758" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10" />
      </concept>
      <concept>
        <code value="OMIM:608762" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608763" />
        <display value="EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:608765" />
        <display value="SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608768" />
        <display value="SPINOCEREBELLAR ATAXIA 8" />
      </concept>
      <concept>
        <code value="OMIM:608776" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il" />
      </concept>
      <concept>
        <code value="OMIM:608779" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe" />
      </concept>
      <concept>
        <code value="OMIM:608781" />
        <display value="ASPERGER SYNDROME, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608782" />
        <display value="PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608787" />
        <display value="OTOSCLEROSIS 5" />
      </concept>
      <concept>
        <code value="OMIM:608796" />
        <display value="MOYAMOYA DISEASE 3" />
      </concept>
      <concept>
        <code value="OMIM:608799" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie" />
      </concept>
      <concept>
        <code value="OMIM:608800" />
        <display value="SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608804" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 2" />
      </concept>
      <concept>
        <code value="OMIM:608805" />
        <display value="AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:608807" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 10" />
      </concept>
      <concept>
        <code value="OMIM:608808" />
        <display value="TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 1" />
      </concept>
      <concept>
        <code value="OMIM:608809" />
        <display value="LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA" />
      </concept>
      <concept>
        <code value="OMIM:608810" />
        <display value="MYOPATHY, MYOFIBRILLAR, 2" />
      </concept>
      <concept>
        <code value="OMIM:608811" />
        <display value="METAPHYSEAL UNDERMODELING, SPONDYLAR DYSPLASIA, AND OVERGROWTH" />
      </concept>
      <concept>
        <code value="OMIM:608812" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:608814" />
        <display value="LATERAL SEMICIRCULAR CANAL MALFORMATION, FAMILIAL, WITH EXTERNAL AND MIDDLE EAR ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:608816" />
        <display value="MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608831" />
        <display value="RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:608836" />
        <display value="CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:608837" />
        <display value="CARNEY COMPLEX VARIANT" />
      </concept>
      <concept>
        <code value="OMIM:608840" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6" />
      </concept>
      <concept>
        <code value="OMIM:608850" />
        <display value="MACULAR DYSTROPHY, RETINAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:608852" />
        <display value="PULMONARY FUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:608864" />
        <display value="OROFACIAL CLEFT 6, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:608874" />
        <display value="OROFACIAL CLEFT 5" />
      </concept>
      <concept>
        <code value="OMIM:608875" />
        <display value="GENE EXPRESSION, VARIATION IN, QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 14" />
      </concept>
      <concept>
        <code value="OMIM:608878" />
        <display value="GENE EXPRESSION, VARIATION IN, QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 20" />
      </concept>
      <concept>
        <code value="OMIM:608885" />
        <display value="STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:608890" />
        <display value="WAARDENBURG SYNDROME, TYPE 2D" />
      </concept>
      <concept>
        <code value="OMIM:608895" />
        <display value="NEUROPATHY, HEREDITARY, WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:608898" />
        <display value="HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:608901" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:608902" />
        <display value="DRUG METABOLISM, POOR, CYP2D6-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:608903" />
        <display value="ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:608904" />
        <display value="ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:608905" />
        <display value="ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:608906" />
        <display value="ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:608907" />
        <display value="ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:608908" />
        <display value="MYOPIA 6" />
      </concept>
      <concept>
        <code value="OMIM:608911" />
        <display value="CHOANAL ATRESIA, POSTERIOR" />
      </concept>
      <concept>
        <code value="OMIM:608930" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL" />
      </concept>
      <concept>
        <code value="OMIM:608931" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:608932" />
        <display value="KERATOCONUS 2" />
      </concept>
      <concept>
        <code value="OMIM:608935" />
        <display value="LUNG CANCER SUSCEPTIBILITY 1" />
      </concept>
      <concept>
        <code value="OMIM:608940" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:608957" />
        <display value="CD8 DEFICIENCY, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:608970" />
        <display value="MACULAR DYSTROPHY, PATTERNED, 2" />
      </concept>
      <concept>
        <code value="OMIM:608971" />
        <display value="SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:608978" />
        <display value="MEACHAM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:608980" />
        <display value="BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:608982" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:608984" />
        <display value="ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:608988" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:608995" />
        <display value="DYSLEXIA, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:608996" />
        <display value="PREMATURE OVARIAN FAILURE 3" />
      </concept>
      <concept>
        <code value="OMIM:609006" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT" />
      </concept>
      <concept>
        <code value="OMIM:609008" />
        <display value="MARFANOID HABITUS WITH SITUS INVERSUS" />
      </concept>
      <concept>
        <code value="OMIM:609015" />
        <display value="MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:609016" />
        <display value="LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:609021" />
        <display value="PERIPHERAL CONE DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:609026" />
        <display value="CATARACT 28" />
      </concept>
      <concept>
        <code value="OMIM:609027" />
        <display value="BLOOD GROUP, INDIAN SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:609029" />
        <display value="EMANUEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609033" />
        <display value="POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA" />
      </concept>
      <concept>
        <code value="OMIM:609037" />
        <display value="MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE" />
      </concept>
      <concept>
        <code value="OMIM:609039" />
        <display value="NARCOLEPSY 3" />
      </concept>
      <concept>
        <code value="OMIM:609040" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9" />
      </concept>
      <concept>
        <code value="OMIM:609041" />
        <display value="SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:609047" />
        <display value="SKELETAL DYSPLASIA, RHIZOMELIC, WITH RETINITIS PIGMENTOSA" />
      </concept>
      <concept>
        <code value="OMIM:609048" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:609049" />
        <display value="PIERSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609052" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4" />
      </concept>
      <concept>
        <code value="OMIM:609053" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP I" />
      </concept>
      <concept>
        <code value="OMIM:609054" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP J" />
      </concept>
      <concept>
        <code value="OMIM:609055" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 9" />
      </concept>
      <concept>
        <code value="OMIM:609056" />
        <display value="SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609057" />
        <display value="NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:609060" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1" />
      </concept>
      <concept>
        <code value="OMIM:609069" />
        <display value="PANCREATIC AND CEREBELLAR AGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:609070" />
        <display value="HEMOGLOBIN, HIGH ALTITUDE ADAPTATION" />
      </concept>
      <concept>
        <code value="OMIM:609113" />
        <display value="TELOMERE LENGTH, MEAN LEUKOCYTE" />
      </concept>
      <concept>
        <code value="OMIM:609115" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 3" />
      </concept>
      <concept>
        <code value="OMIM:609116" />
        <display value="RESPIRATORY RHYTHMICITY IN SLEEP" />
      </concept>
      <concept>
        <code value="OMIM:609122" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 3" />
      </concept>
      <concept>
        <code value="OMIM:609128" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:609129" />
        <display value="AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1" />
      </concept>
      <concept>
        <code value="OMIM:609135" />
        <display value="APLASTIC ANEMIA" />
      </concept>
      <concept>
        <code value="OMIM:609136" />
        <display value="PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:609140" />
        <display value="CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2" />
      </concept>
      <concept>
        <code value="OMIM:609141" />
        <display value="CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3" />
      </concept>
      <concept>
        <code value="OMIM:609148" />
        <display value="MALARIA, MILD, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:609152" />
        <display value="HYPERTHYROIDISM, NONAUTOIMMUNE" />
      </concept>
      <concept>
        <code value="OMIM:609153" />
        <display value="PSEUDOHYPERKALEMIA, FAMILIAL, 2, DUE TO RED CELL LEAK" />
      </concept>
      <concept>
        <code value="OMIM:609161" />
        <display value="STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:609162" />
        <display value="CZECH DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:609164" />
        <display value="UMBILICUS, FAMILIAL FLAT" />
      </concept>
      <concept>
        <code value="OMIM:609165" />
        <display value="ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR" />
      </concept>
      <concept>
        <code value="OMIM:609166" />
        <display value="BRANCHIOGENIC-DEAFNESS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609179" />
        <display value="MIGRAINE WITH AURA, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:609180" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If" />
      </concept>
      <concept>
        <code value="OMIM:609192" />
        <display value="LOEYS-DIETZ SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:609195" />
        <display value="SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:609197" />
        <display value="GLUCOCORTICOID DEFICIENCY 3" />
      </concept>
      <concept>
        <code value="OMIM:609200" />
        <display value="MYOPATHY, MYOFIBRILLAR, 3" />
      </concept>
      <concept>
        <code value="OMIM:609218" />
        <display value="FOVEAL HYPOPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:609220" />
        <display value="BRUCK SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:609222" />
        <display value="DANDY-WALKER MALFORMATION WITH OCCIPITAL CEPHALOCELE, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:609223" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGER TYPE" />
      </concept>
      <concept>
        <code value="OMIM:609227" />
        <display value="GRISCELLI SYNDROME, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:609241" />
        <display value="SCHINDLER DISEASE, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:609242" />
        <display value="KANZAKI DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:609250" />
        <display value="HYPOTRICHOSIS, PROGRESSIVE PATTERNED SCALP, WITH WIRY HAIR, ONYCHOLYSIS, AND CLEFT LIP/PALATE" />
      </concept>
      <concept>
        <code value="OMIM:609253" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:609254" />
        <display value="SENIOR-LOKEN SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:609255" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:609256" />
        <display value="MYOPIA 7" />
      </concept>
      <concept>
        <code value="OMIM:609257" />
        <display value="MYOPIA 8" />
      </concept>
      <concept>
        <code value="OMIM:609258" />
        <display value="MYOPIA 9" />
      </concept>
      <concept>
        <code value="OMIM:609259" />
        <display value="MYOPIA 10" />
      </concept>
      <concept>
        <code value="OMIM:609260" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A" />
      </concept>
      <concept>
        <code value="OMIM:609261" />
        <display value="STUTTERING, FAMILIAL PERSISTENT, 2" />
      </concept>
      <concept>
        <code value="OMIM:609265" />
        <display value="LI-FRAUMENI SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:609270" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7" />
      </concept>
      <concept>
        <code value="OMIM:609271" />
        <display value="KERATOCONUS 4" />
      </concept>
      <concept>
        <code value="OMIM:609273" />
        <display value="NEMALINE MYOPATHY 6" />
      </concept>
      <concept>
        <code value="OMIM:609283" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:609284" />
        <display value="NEMALINE MYOPATHY 1" />
      </concept>
      <concept>
        <code value="OMIM:609285" />
        <display value="NEMALINE MYOPATHY 4" />
      </concept>
      <concept>
        <code value="OMIM:609286" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3" />
      </concept>
      <concept>
        <code value="OMIM:609289" />
        <display value="SYNCOPE, FAMILIAL VASOVAGAL" />
      </concept>
      <concept>
        <code value="OMIM:609296" />
        <display value="B-CELL IMMUNODEFICIENCY, DISTAL LIMB ANOMALIES, AND UROGENITAL MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:609299" />
        <display value="PROSTATE CANCER, HEREDITARY, 5" />
      </concept>
      <concept>
        <code value="OMIM:609304" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3" />
      </concept>
      <concept>
        <code value="OMIM:609306" />
        <display value="SPINOCEREBELLAR ATAXIA 26" />
      </concept>
      <concept>
        <code value="OMIM:609307" />
        <display value="SPINOCEREBELLAR ATAXIA 27" />
      </concept>
      <concept>
        <code value="OMIM:609308" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1" />
      </concept>
      <concept>
        <code value="OMIM:609310" />
        <display value="COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:609311" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H" />
      </concept>
      <concept>
        <code value="OMIM:609313" />
        <display value="MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA" />
      </concept>
      <concept>
        <code value="OMIM:609319" />
        <display value="HEMATOCRIT/HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:609320" />
        <display value="HEMATOCRIT/HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:609322" />
        <display value="RHABDOID TUMOR PREDISPOSITION SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:609324" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:609325" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES" />
      </concept>
      <concept>
        <code value="OMIM:609334" />
        <display value="CHROMOSOME 18 PERICENTRIC INVERSION" />
      </concept>
      <concept>
        <code value="OMIM:609338" />
        <display value="CAROTID INTIMAL MEDIAL THICKNESS 1" />
      </concept>
      <concept>
        <code value="OMIM:609340" />
        <display value="SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:609345" />
        <display value="CEREBRORENODIGITAL SYNDROME WITH LIMB MALFORMATIONS AND TRIRADIATE ACETABULA" />
      </concept>
      <concept>
        <code value="OMIM:609352" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX WITH MIGRATORY CIRCINATE ERYTHEMA" />
      </concept>
      <concept>
        <code value="OMIM:609354" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:609363" />
        <display value="COLLOID CYSTS OF THIRD VENTRICLE" />
      </concept>
      <concept>
        <code value="OMIM:609376" />
        <display value="CATARACT 35" />
      </concept>
      <concept>
        <code value="OMIM:609378" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:609384" />
        <display value="FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3C" />
      </concept>
      <concept>
        <code value="OMIM:609400" />
        <display value="AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:609402" />
        <display value="PREECLAMPSIA/ECLAMPSIA 2" />
      </concept>
      <concept>
        <code value="OMIM:609403" />
        <display value="PREECLAMPSIA/ECLAMPSIA 3" />
      </concept>
      <concept>
        <code value="OMIM:609404" />
        <display value="PREECLAMPSIA/ECLAMPSIA 4" />
      </concept>
      <concept>
        <code value="OMIM:609408" />
        <display value="HOLOPROSENCEPHALY 8" />
      </concept>
      <concept>
        <code value="OMIM:609423" />
        <display value="HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:609425" />
        <display value="CHROMOSOME 3q29 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609428" />
        <display value="TUKEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609432" />
        <display value="SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION" />
      </concept>
      <concept>
        <code value="OMIM:609438" />
        <display value="MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIAL BLOCK" />
      </concept>
      <concept>
        <code value="OMIM:609439" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 48" />
      </concept>
      <concept>
        <code value="OMIM:609441" />
        <display value="ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:609442" />
        <display value="VALPROATE EMBRYOPATHY, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:609446" />
        <display value="PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY" />
      </concept>
      <concept>
        <code value="OMIM:609452" />
        <display value="MYOPATHY, MYOFIBRILLAR, 4" />
      </concept>
      <concept>
        <code value="OMIM:609454" />
        <display value="SUPRANUCLEAR PALSY, PROGRESSIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:609456" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:609460" />
        <display value="GOLDBERG-SHPRINTZEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609465" />
        <display value="AL-GAZALI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609466" />
        <display value="CLEFT PALATE, MIDFACIAL HYPOPLASIA, TRIANGULAR FACIES, AND SENSORINEURAL HEARING LOSS" />
      </concept>
      <concept>
        <code value="OMIM:609469" />
        <display value="NEPHROPATHY, PROGRESSIVE, WITH DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:609470" />
        <display value="LEFT VENTRICULAR NONCOMPACTION 2" />
      </concept>
      <concept>
        <code value="OMIM:609500" />
        <display value="MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:609508" />
        <display value="STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR" />
      </concept>
      <concept>
        <code value="OMIM:609515" />
        <display value="IRIDOGONIODYSGENESIS AND SKELETAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:609524" />
        <display value="MYOPATHY, MYOFIBRILLAR, 5" />
      </concept>
      <concept>
        <code value="OMIM:609528" />
        <display value="CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609529" />
        <display value="IMMUNOGLOBULIN A DEFICIENCY 2" />
      </concept>
      <concept>
        <code value="OMIM:609532" />
        <display value="HEPATITIS C VIRUS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:609533" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 23" />
      </concept>
      <concept>
        <code value="OMIM:609535" />
        <display value="DRUG METABOLISM, POOR, CYP2C19-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:609536" />
        <display value="COMPLEMENT COMPONENT 5 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:609537" />
        <display value="LIPOMYELOMENINGOCELE" />
      </concept>
      <concept>
        <code value="OMIM:609541" />
        <display value="SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:609545" />
        <display value="OMPHALOCELE, DIAPHRAGMATIC HERNIA, AND RADIAL RAY DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:609549" />
        <display value="NANOPHTHALMOS 2" />
      </concept>
      <concept>
        <code value="OMIM:609558" />
        <display value="PROSTATE CANCER, HEREDITARY, 6" />
      </concept>
      <concept>
        <code value="OMIM:609560" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:609566" />
        <display value="PARIETAL FORAMINA 3" />
      </concept>
      <concept>
        <code value="OMIM:609570" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:609572" />
        <display value="PHOTOPAROXYSMAL RESPONSE 2" />
      </concept>
      <concept>
        <code value="OMIM:609573" />
        <display value="PHOTOPAROXYSMAL RESPONSE 3" />
      </concept>
      <concept>
        <code value="OMIM:609578" />
        <display value="CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:609579" />
        <display value="SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:609583" />
        <display value="JOUBERT SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:609597" />
        <display value="PARIETAL FORAMINA 2" />
      </concept>
      <concept>
        <code value="OMIM:609612" />
        <display value="FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH SYNERGISTIC DIVERGENCE" />
      </concept>
      <concept>
        <code value="OMIM:609616" />
        <display value="SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATE CALCIFICATIONS, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:609620" />
        <display value="SHORT QT SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:609621" />
        <display value="SHORT QT SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:609622" />
        <display value="SHORT QT SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:609625" />
        <display value="CHROMOSOME 10q26 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609628" />
        <display value="MAJEED SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609629" />
        <display value="VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:609630" />
        <display value="LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:609633" />
        <display value="MAJOR AFFECTIVE DISORDER 3" />
      </concept>
      <concept>
        <code value="OMIM:609634" />
        <display value="MIGRAINE, FAMILIAL HEMIPLEGIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:609636" />
        <display value="ALZHEIMER DISEASE 10" />
      </concept>
      <concept>
        <code value="OMIM:609637" />
        <display value="HOLOPROSENCEPHALY 5" />
      </concept>
      <concept>
        <code value="OMIM:609638" />
        <display value="EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC" />
      </concept>
      <concept>
        <code value="OMIM:609640" />
        <display value="FRIAS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609643" />
        <display value="NGUYEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609646" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 42" />
      </concept>
      <concept>
        <code value="OMIM:609647" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 46" />
      </concept>
      <concept>
        <code value="OMIM:609649" />
        <display value="TRICHILEMMAL CYST 1" />
      </concept>
      <concept>
        <code value="OMIM:609654" />
        <display value="SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:609655" />
        <display value="TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS" />
      </concept>
      <concept>
        <code value="OMIM:609656" />
        <display value="BONE SIZE QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:609657" />
        <display value="BONE SIZE QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:609670" />
        <display value="MIGRAINE WITH AURA, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:609698" />
        <display value="THYROID HORMONE METABOLISM, ABNORMAL" />
      </concept>
      <concept>
        <code value="OMIM:609706" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 53" />
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      <concept>
        <code value="OMIM:609708" />
        <display value="LIPOPROTEIN LIPASE" />
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      <concept>
        <code value="OMIM:609727" />
        <display value="SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:609734" />
        <display value="OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR" />
      </concept>
      <concept>
        <code value="OMIM:609741" />
        <display value="CATARACT 22, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:609745" />
        <display value="GLAUCOMA 1, OPEN ANGLE, I" />
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      <concept>
        <code value="OMIM:609750" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:609753" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:609754" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:609755" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:609757" />
        <display value="WILLIAMS-BEUREN REGION DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:609782" />
        <display value="AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:609790" />
        <display value="ALZHEIMER DISEASE 11" />
      </concept>
      <concept>
        <code value="OMIM:609796" />
        <display value="PEELING SKIN SYNDROME 2" />
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      <concept>
        <code value="OMIM:609800" />
        <display value="GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:609808" />
        <display value="HAMARTOMA, PRECALCANEAL CONGENITAL FIBROLIPOMATOUS" />
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      <concept>
        <code value="OMIM:609812" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:609813" />
        <display value="SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE" />
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      <concept>
        <code value="OMIM:609814" />
        <display value="COMPLEMENT FACTOR H DEFICIENCY" />
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      <concept>
        <code value="OMIM:609815" />
        <display value="ZYGODACTYLY 1" />
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      <concept>
        <code value="OMIM:609817" />
        <display value="VASCULITIS, LYMPHOCYTIC, CUTANEOUS SMALL VESSEL" />
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      <concept>
        <code value="OMIM:609820" />
        <display value="ERYTHROCYTOSIS, FAMILIAL, 3" />
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      <concept>
        <code value="OMIM:609821" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 8" />
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      <concept>
        <code value="OMIM:609822" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 7" />
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      <concept>
        <code value="OMIM:609823" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 28" />
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      <concept>
        <code value="OMIM:609876" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 6" />
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      <concept>
        <code value="OMIM:609886" />
        <display value="GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA" />
      </concept>
      <concept>
        <code value="OMIM:609887" />
        <display value="GLAUCOMA 1, OPEN ANGLE, G" />
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      <concept>
        <code value="OMIM:609888" />
        <display value="LEPROSY, SUSCEPTIBILITY TO, 1" />
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      <concept>
        <code value="OMIM:609889" />
        <display value="ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION, SEVERE CYTOMEGALOVIRUS INFECTION, AND AUTOIMMUNITY" />
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      <concept>
        <code value="OMIM:609893" />
        <display value="HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3" />
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      <concept>
        <code value="OMIM:609903" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 5" />
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      <concept>
        <code value="OMIM:609909" />
        <display value="CARDIOMYOPATHY, DILATED, 1P" />
      </concept>
      <concept>
        <code value="OMIM:609913" />
        <display value="RETINITIS PIGMENTOSA 32" />
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      <concept>
        <code value="OMIM:609915" />
        <display value="CARDIOMYOPATHY, DILATED, 1Q" />
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      <concept>
        <code value="OMIM:609918" />
        <display value="GALLBLADDER DISEASE 2" />
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      <concept>
        <code value="OMIM:609919" />
        <display value="GALLBLADDER DISEASE 3" />
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      <concept>
        <code value="OMIM:609923" />
        <display value="RETINITIS PIGMENTOSA 31" />
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      <concept>
        <code value="OMIM:609924" />
        <display value="AMINOACYLASE 1 DEFICIENCY" />
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      <concept>
        <code value="OMIM:609939" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6" />
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      <concept>
        <code value="OMIM:609941" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 51" />
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      <concept>
        <code value="OMIM:609942" />
        <display value="NOONAN SYNDROME 3" />
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      <concept>
        <code value="OMIM:609943" />
        <display value="HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES" />
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      <concept>
        <code value="OMIM:609944" />
        <display value="ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES" />
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      <concept>
        <code value="OMIM:609945" />
        <display value="BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA" />
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      <concept>
        <code value="OMIM:609946" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 47" />
      </concept>
      <concept>
        <code value="OMIM:609952" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 55" />
      </concept>
      <concept>
        <code value="OMIM:609954" />
        <display value="ASPERGER SYNDROME, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:609955" />
        <display value="FIBROMATOSIS, GINGIVAL, 3" />
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      <concept>
        <code value="OMIM:609958" />
        <display value="ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:609965" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 53" />
      </concept>
      <concept>
        <code value="OMIM:609968" />
        <display value="HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:609975" />
        <display value="HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:609981" />
        <display value="IMMUNODEFICIENCY 54" />
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      <concept>
        <code value="OMIM:609985" />
        <display value="PANIC DISORDER 3" />
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      <concept>
        <code value="OMIM:609989" />
        <display value="METAPHYSEAL CHONDRODYSPLASIA WITH CONE-SHAPED EPIPHYSES, NORMAL HAIR, AND NORMAL HANDS" />
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      <concept>
        <code value="OMIM:609990" />
        <display value="TRICHOSCYPHODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:609993" />
        <display value="OSTEOSCLEROSIS WITH ICHTHYOSIS AND PREMATURE OVARIAN FAILURE" />
      </concept>
      <concept>
        <code value="OMIM:609994" />
        <display value="MYOPIA 11, AUTOSOMAL DOMINANT" />
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      <concept>
        <code value="OMIM:609995" />
        <display value="MYOPIA 12, AUTOSOMAL DOMINANT" />
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      <concept>
        <code value="OMIM:610001" />
        <display value="ARTHROGRYPOSIS MULTIPLEX WITH DEAFNESS, INGUINAL HERNIAS, AND EARLY DEATH" />
      </concept>
      <concept>
        <code value="OMIM:610003" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT" />
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      <concept>
        <code value="OMIM:610006" />
        <display value="2-METHYLBUTYRYL-CoA DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610015" />
        <display value="GLUTAMINE DEFICIENCY, CONGENITAL" />
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      <concept>
        <code value="OMIM:610017" />
        <display value="MULTIPLE SYNOSTOSES SYNDROME 2" />
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      <concept>
        <code value="OMIM:610019" />
        <display value="CATARACT 18" />
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      <concept>
        <code value="OMIM:610021" />
        <display value="HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7" />
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      <concept>
        <code value="OMIM:610023" />
        <display value="BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:610024" />
        <display value="RETINAL CONE DYSTROPHY 3A" />
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      <concept>
        <code value="OMIM:610031" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7" />
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      <concept>
        <code value="OMIM:610042" />
        <display value="PITT-HOPKINS-LIKE SYNDROME 1" />
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      <concept>
        <code value="OMIM:610048" />
        <display value="CORNEAL DYSTROPHY, CONGENITAL STROMAL" />
      </concept>
      <concept>
        <code value="OMIM:610064" />
        <display value="OPIOID DEPENDENCE, SUSCEPTIBILITY TO, 1" />
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      <concept>
        <code value="OMIM:610065" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:610066" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:610069" />
        <display value="POLYPOSIS SYNDROME, HEREDITARY MIXED, 2" />
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      <concept>
        <code value="OMIM:610071" />
        <display value="HYPERPARATHYROIDISM 3" />
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      <concept>
        <code value="OMIM:610090" />
        <display value="PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610092" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 3" />
      </concept>
      <concept>
        <code value="OMIM:610093" />
        <display value="MICROPHTHALMIA, ISOLATED 2" />
      </concept>
      <concept>
        <code value="OMIM:610099" />
        <display value="MYOPATHY, DISTAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:610100" />
        <display value="GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:610102" />
        <display value="COMPLEMENT COMPONENT 7 DEFICIENCY" />
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      <concept>
        <code value="OMIM:610114" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 8" />
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      <concept>
        <code value="OMIM:610125" />
        <display value="MICROPHTHALMIA, SYNDROMIC 5" />
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      <concept>
        <code value="OMIM:610127" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 10" />
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      <concept>
        <code value="OMIM:610131" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4" />
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      <concept>
        <code value="OMIM:610136" />
        <display value="DEVRIENDT SYNDROME" />
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      <concept>
        <code value="OMIM:610140" />
        <display value="HEART-HAND SYNDROME, SLOVENIAN TYPE" />
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      <concept>
        <code value="OMIM:610141" />
        <display value="QT INTERVAL, VARIATION IN" />
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      <concept>
        <code value="OMIM:610143" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 62" />
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      <concept>
        <code value="OMIM:610149" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 7" />
      </concept>
      <concept>
        <code value="OMIM:610153" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 49" />
      </concept>
      <concept>
        <code value="OMIM:610154" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 44" />
      </concept>
      <concept>
        <code value="OMIM:610155" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 19" />
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      <concept>
        <code value="OMIM:610156" />
        <display value="MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:610157" />
        <display value="HEAT-SHOCK RNA 1" />
      </concept>
      <concept>
        <code value="OMIM:610158" />
        <display value="CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:610163" />
        <display value="IMMUNODEFICIENCY 25" />
      </concept>
      <concept>
        <code value="OMIM:610168" />
        <display value="LOEYS-DIETZ SYNDROME 2" />
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      <concept>
        <code value="OMIM:610170" />
        <display value="KYPHOSCOLIOSIS 1" />
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      <concept>
        <code value="OMIM:610181" />
        <display value="AICARDI-GOUTIERES SYNDROME 2" />
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      <concept>
        <code value="OMIM:610185" />
        <display value="CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:610187" />
        <display value="DIAPHRAGMATIC HERNIA 3" />
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      <concept>
        <code value="OMIM:610188" />
        <display value="JOUBERT SYNDROME 5" />
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      <concept>
        <code value="OMIM:610189" />
        <display value="SENIOR-LOKEN SYNDROME 6" />
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      <concept>
        <code value="OMIM:610193" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10" />
      </concept>
      <concept>
        <code value="OMIM:610198" />
        <display value="3-METHYLGLUTACONIC ACIDURIA, TYPE V" />
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      <concept>
        <code value="OMIM:610199" />
        <display value="DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM" />
      </concept>
      <concept>
        <code value="OMIM:610202" />
        <display value="CATARACT 21, MULTIPLE TYPES" />
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      <concept>
        <code value="OMIM:610204" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 5" />
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      <concept>
        <code value="OMIM:610205" />
        <display value="ALAGILLE SYNDROME 2" />
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      <concept>
        <code value="OMIM:610208" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10" />
      </concept>
      <concept>
        <code value="OMIM:610209" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11" />
      </concept>
      <concept>
        <code value="OMIM:610212" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 66" />
      </concept>
      <concept>
        <code value="OMIM:610213" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 4" />
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      <concept>
        <code value="OMIM:610217" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B" />
      </concept>
      <concept>
        <code value="OMIM:610220" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 59" />
      </concept>
      <concept>
        <code value="OMIM:610227" />
        <display value="SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS" />
      </concept>
      <concept>
        <code value="OMIM:610234" />
        <display value="SYNPOLYDACTYLY 3" />
      </concept>
      <concept>
        <code value="OMIM:610239" />
        <display value="HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:610244" />
        <display value="SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:610245" />
        <display value="SPINOCEREBELLAR ATAXIA 23" />
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      <concept>
        <code value="OMIM:610246" />
        <display value="SPINOCEREBELLAR ATAXIA 28" />
      </concept>
      <concept>
        <code value="OMIM:610247" />
        <display value="ESOPHAGITIS, EOSINOPHILIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:610248" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 65" />
      </concept>
      <concept>
        <code value="OMIM:610250" />
        <display value="SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:610251" />
        <display value="ALCOHOL SENSITIVITY, ACUTE" />
      </concept>
      <concept>
        <code value="OMIM:610253" />
        <display value="KLEEFSTRA SYNDROME 1" />
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      <concept>
        <code value="OMIM:610256" />
        <display value="ANTERIOR SEGMENT DYSGENESIS 2" />
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      <concept>
        <code value="OMIM:610260" />
        <display value="PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 2" />
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      <concept>
        <code value="OMIM:610261" />
        <display value="HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:610262" />
        <display value="HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:610265" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 67" />
      </concept>
      <concept>
        <code value="OMIM:610279" />
        <display value="PACHYGYRIA, FRONTOTEMPORAL" />
      </concept>
      <concept>
        <code value="OMIM:610282" />
        <display value="RETINITIS PIGMENTOSA 35" />
      </concept>
      <concept>
        <code value="OMIM:610283" />
        <display value="CONE-ROD DYSTROPHY 10" />
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      <concept>
        <code value="OMIM:610293" />
        <display value="GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610294" />
        <display value="INTELLIGENCE QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:610295" />
        <display value="INTELLIGENCE QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:610297" />
        <display value="PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:610313" />
        <display value="CRISPONI/COLD-INDUCED SWEATING SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:610319" />
        <display value="RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA" />
      </concept>
      <concept>
        <code value="OMIM:610320" />
        <display value="MYOPIA 14" />
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      <concept>
        <code value="OMIM:610321" />
        <display value="PROSTATE CANCER, HEREDITARY, 7" />
      </concept>
      <concept>
        <code value="OMIM:610329" />
        <display value="AICARDI-GOUTIERES SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:610333" />
        <display value="AICARDI-GOUTIERES SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:610338" />
        <display value="RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:610353" />
        <display value="EPILEPSY, NOCTURNAL FRONTAL LOBE, 4" />
      </concept>
      <concept>
        <code value="OMIM:610356" />
        <display value="RETINAL CONE DYSTROPHY 3B" />
      </concept>
      <concept>
        <code value="OMIM:610357" />
        <display value="SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:610359" />
        <display value="RETINITIS PIGMENTOSA 33" />
      </concept>
      <concept>
        <code value="OMIM:610361" />
        <display value="OROFACIAL CLEFT 9" />
      </concept>
      <concept>
        <code value="OMIM:610370" />
        <display value="DIARRHEA 4, MALABSORPTIVE, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:610374" />
        <display value="DIABETES MELLITUS, TRANSIENT NEONATAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:610377" />
        <display value="MEVALONIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:610379" />
        <display value="WEST NILE VIRUS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:610381" />
        <display value="CONE-ROD DYSTROPHY 11" />
      </concept>
      <concept>
        <code value="OMIM:610382" />
        <display value="PROSOPAGNOSIA, HEREDITARY" />
      </concept>
      <concept>
        <code value="OMIM:610419" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 68" />
      </concept>
      <concept>
        <code value="OMIM:610420" />
        <display value="PREAURICULAR TAG, ISOLATED, AUTOSOMAL DOMINANT, 1" />
      </concept>
      <concept>
        <code value="OMIM:610422" />
        <display value="ALOPECIA-MENTAL RETARDATION SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:610424" />
        <display value="HEPATITIS B VIRUS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:610425" />
        <display value="CATARACT 23, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:610427" />
        <display value="CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:610430" />
        <display value="MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:610438" />
        <display value="RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:610439" />
        <display value="RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:610441" />
        <display value="TESTICULAR MICROLITHIASIS" />
      </concept>
      <concept>
        <code value="OMIM:610442" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE" />
      </concept>
      <concept>
        <code value="OMIM:610443" />
        <display value="KOOLEN-DE VRIES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:610444" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3" />
      </concept>
      <concept>
        <code value="OMIM:610445" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1" />
      </concept>
      <concept>
        <code value="OMIM:610446" />
        <display value="BURULI ULCER, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:610448" />
        <display value="CHILBLAIN LUPUS 1" />
      </concept>
      <concept>
        <code value="OMIM:610452" />
        <display value="MUTAGEN SENSITIVITY" />
      </concept>
      <concept>
        <code value="OMIM:610455" />
        <display value="TUMORAL CALCINOSIS, NORMOPHOSPHATEMIC, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:610460" />
        <display value="THIOPURINES, POOR METABOLISM OF, 1" />
      </concept>
      <concept>
        <code value="OMIM:610474" />
        <display value="CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:610475" />
        <display value="PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:610476" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11" />
      </concept>
      <concept>
        <code value="OMIM:610478" />
        <display value="RETINAL CONE DYSTROPHY 4" />
      </concept>
      <concept>
        <code value="OMIM:610483" />
        <display value="AGAMMAGLOBULINEMIA, MICROCEPHALY, AND SEVERE DERMATITIS" />
      </concept>
      <concept>
        <code value="OMIM:610489" />
        <display value="PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1" />
      </concept>
      <concept>
        <code value="OMIM:610498" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2" />
      </concept>
      <concept>
        <code value="OMIM:610504" />
        <display value="PRETERM PREMATURE RUPTURE OF THE MEMBRANES" />
      </concept>
      <concept>
        <code value="OMIM:610505" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3" />
      </concept>
      <concept>
        <code value="OMIM:610508" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:610532" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 5" />
      </concept>
      <concept>
        <code value="OMIM:610535" />
        <display value="GLAUCOMA 1, OPEN ANGLE, M" />
      </concept>
      <concept>
        <code value="OMIM:610536" />
        <display value="MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:610539" />
        <display value="GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610542" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 12" />
      </concept>
      <concept>
        <code value="OMIM:610543" />
        <display value="CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL" />
      </concept>
      <concept>
        <code value="OMIM:610549" />
        <display value="DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS" />
      </concept>
      <concept>
        <code value="OMIM:610551" />
        <display value="ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:610582" />
        <display value="DIABETES MELLITUS, TRANSIENT NEONATAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:610599" />
        <display value="RETINITIS PIGMENTOSA 36" />
      </concept>
      <concept>
        <code value="OMIM:610600" />
        <display value="CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610612" />
        <display value="LEBER CONGENITAL AMAUROSIS 12" />
      </concept>
      <concept>
        <code value="OMIM:610618" />
        <display value="ANGIOEDEMA, HEREDITARY, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:610623" />
        <display value="CATARACT 11, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:610628" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:610629" />
        <display value="DIAMOND-BLACKFAN ANEMIA 3" />
      </concept>
      <concept>
        <code value="OMIM:610644" />
        <display value="PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL" />
      </concept>
      <concept>
        <code value="OMIM:610649" />
        <display value="BONE SIZE QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:610651" />
        <display value="XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B" />
      </concept>
      <concept>
        <code value="OMIM:610655" />
        <display value="TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:610676" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:610678" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4" />
      </concept>
      <concept>
        <code value="OMIM:610680" />
        <display value="HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:610682" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE VII" />
      </concept>
      <concept>
        <code value="OMIM:610685" />
        <display value="SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 2" />
      </concept>
      <concept>
        <code value="OMIM:610687" />
        <display value="NEMALINE MYOPATHY 7" />
      </concept>
      <concept>
        <code value="OMIM:610688" />
        <display value="JOUBERT SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:610698" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 4" />
      </concept>
      <concept>
        <code value="OMIM:610706" />
        <display value="DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA" />
      </concept>
      <concept>
        <code value="OMIM:610707" />
        <display value="PSORIASIS 8, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:610708" />
        <display value="OPTIC ATROPHY 5" />
      </concept>
      <concept>
        <code value="OMIM:610713" />
        <display value="BRACHYDACTYLY-SYNDACTYLY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:610717" />
        <display value="NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:610725" />
        <display value="NEPHROTIC SYNDROME, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:610733" />
        <display value="NOONAN SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:610738" />
        <display value="NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:610743" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8" />
      </concept>
      <concept>
        <code value="OMIM:610744" />
        <display value="IRIS PATTERN" />
      </concept>
      <concept>
        <code value="OMIM:610753" />
        <display value="ALOPECIA AREATA 2" />
      </concept>
      <concept>
        <code value="OMIM:610755" />
        <display value="MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:610756" />
        <display value="CEREBROOCULOFACIOSKELETAL SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:610758" />
        <display value="CEREBROOCULOFACIOSKELETAL SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:610759" />
        <display value="CORNELIA DE LANGE SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:610760" />
        <display value="CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:610761" />
        <display value="HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:610762" />
        <display value="HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6" />
      </concept>
      <concept>
        <code value="OMIM:610768" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im" />
      </concept>
      <concept>
        <code value="OMIM:610773" />
        <display value="MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610797" />
        <display value="EPIPHYSEAL DYSPLASIA, BAUMANN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:610798" />
        <display value="IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN" />
      </concept>
      <concept>
        <code value="OMIM:610799" />
        <display value="INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 1" />
      </concept>
      <concept>
        <code value="OMIM:610805" />
        <display value="CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 1" />
      </concept>
      <concept>
        <code value="OMIM:610828" />
        <display value="HOLOPROSENCEPHALY 7" />
      </concept>
      <concept>
        <code value="OMIM:610829" />
        <display value="HOLOPROSENCEPHALY 9" />
      </concept>
      <concept>
        <code value="OMIM:610830" />
        <display value="POLYOSTEOLYSIS-HYPEROSTOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:610832" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP N" />
      </concept>
      <concept>
        <code value="OMIM:610836" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 11" />
      </concept>
      <concept>
        <code value="OMIM:610838" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 12" />
      </concept>
      <concept>
        <code value="OMIM:610839" />
        <display value="OSTEOARTHRITIS SUSCEPTIBILITY 4" />
      </concept>
      <concept>
        <code value="OMIM:610840" />
        <display value="MITRAL VALVE PROLAPSE 3" />
      </concept>
      <concept>
        <code value="OMIM:610842" />
        <display value="PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610852" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 6" />
      </concept>
      <concept>
        <code value="OMIM:610871" />
        <display value="SAKODA COMPLEX" />
      </concept>
      <concept>
        <code value="OMIM:610873" />
        <display value="MENARCHE, AGE AT, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:610878" />
        <display value="VESICOURETERAL REFLUX 2" />
      </concept>
      <concept>
        <code value="OMIM:610883" />
        <display value="POTOCKI-LUPSKI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:610896" />
        <display value="BRANCHIOOTORENAL SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:610898" />
        <display value="SUPRANUCLEAR PALSY, PROGRESSIVE, 3" />
      </concept>
      <concept>
        <code value="OMIM:610906" />
        <display value="ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:610908" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 13" />
      </concept>
      <concept>
        <code value="OMIM:610910" />
        <display value="PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED" />
      </concept>
      <concept>
        <code value="OMIM:610913" />
        <display value="SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:610915" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE VIII" />
      </concept>
      <concept>
        <code value="OMIM:610921" />
        <display value="SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3" />
      </concept>
      <concept>
        <code value="OMIM:610926" />
        <display value="TOOTH AGENESIS, SELECTIVE, 5" />
      </concept>
      <concept>
        <code value="OMIM:610927" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:610938" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:610947" />
        <display value="CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:610948" />
        <display value="HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:610951" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 7" />
      </concept>
      <concept>
        <code value="OMIM:610954" />
        <display value="PITT-HOPKINS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:610965" />
        <display value="XFE PROGEROID SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:610967" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:610968" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XI" />
      </concept>
      <concept>
        <code value="OMIM:610978" />
        <display value="CHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM WITH OR WITHOUT PULMONARY DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:610984" />
        <display value="COMPLEMENT FACTOR I DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610988" />
        <display value="LEPROSY, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:610992" />
        <display value="PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:610997" />
        <display value="PROSTATE CANCER, HEREDITARY, 9" />
      </concept>
      <concept>
        <code value="OMIM:611003" />
        <display value="SMOKING AS A QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:611004" />
        <display value="SMOKING AS A QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:611010" />
        <display value="FIBROMATOSIS, GINGIVAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:611014" />
        <display value="HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:611015" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:611016" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 10" />
      </concept>
      <concept>
        <code value="OMIM:611022" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 24" />
      </concept>
      <concept>
        <code value="OMIM:611031" />
        <display value="EPISODIC KINESIGENIC DYSKINESIA 2" />
      </concept>
      <concept>
        <code value="OMIM:611038" />
        <display value="MICROPHTHALMIA, ISOLATED 3" />
      </concept>
      <concept>
        <code value="OMIM:611040" />
        <display value="MICROPHTHALMIA, ISOLATED 5" />
      </concept>
      <concept>
        <code value="OMIM:611046" />
        <display value="MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:611064" />
        <display value="ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:611067" />
        <display value="SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4" />
      </concept>
      <concept>
        <code value="OMIM:611073" />
        <display value="ALZHEIMER DISEASE 12" />
      </concept>
      <concept>
        <code value="OMIM:611081" />
        <display value="INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 10" />
      </concept>
      <concept>
        <code value="OMIM:611087" />
        <display value="POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY" />
      </concept>
      <concept>
        <code value="OMIM:611090" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12" />
      </concept>
      <concept>
        <code value="OMIM:611091" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5" />
      </concept>
      <concept>
        <code value="OMIM:611092" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6" />
      </concept>
      <concept>
        <code value="OMIM:611093" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7" />
      </concept>
      <concept>
        <code value="OMIM:611095" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 9" />
      </concept>
      <concept>
        <code value="OMIM:611096" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 10" />
      </concept>
      <concept>
        <code value="OMIM:611097" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 11" />
      </concept>
      <concept>
        <code value="OMIM:611100" />
        <display value="PROSTATE CANCER, HEREDITARY, 10" />
      </concept>
      <concept>
        <code value="OMIM:611102" />
        <display value="DEAFNESS-INFERTILITY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611105" />
        <display value="LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION" />
      </concept>
      <concept>
        <code value="OMIM:611107" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4" />
      </concept>
      <concept>
        <code value="OMIM:611109" />
        <display value="CINNAMON ODOR, PLEASANTNESS OF" />
      </concept>
      <concept>
        <code value="OMIM:611126" />
        <display value="MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:611131" />
        <display value="RETINITIS PIGMENTOSA 37" />
      </concept>
      <concept>
        <code value="OMIM:611134" />
        <display value="MECKEL SYNDROME, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:611136" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13" />
      </concept>
      <concept>
        <code value="OMIM:611139" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:611147" />
        <display value="PAROXYSMAL NONKINESIGENIC DYSKINESIA 2" />
      </concept>
      <concept>
        <code value="OMIM:611152" />
        <display value="ALZHEIMER DISEASE 13" />
      </concept>
      <concept>
        <code value="OMIM:611154" />
        <display value="ALZHEIMER DISEASE 14" />
      </concept>
      <concept>
        <code value="OMIM:611155" />
        <display value="ALZHEIMER DISEASE 15" />
      </concept>
      <concept>
        <code value="OMIM:611162" />
        <display value="MALARIA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:611174" />
        <display value="HAMAMY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611182" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh" />
      </concept>
      <concept>
        <code value="OMIM:611185" />
        <display value="RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:611209" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg" />
      </concept>
      <concept>
        <code value="OMIM:611222" />
        <display value="MICROPHTHALMIA, SYNDROMIC 10" />
      </concept>
      <concept>
        <code value="OMIM:611225" />
        <display value="SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:611228" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J" />
      </concept>
      <concept>
        <code value="OMIM:611242" />
        <display value="RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:611247" />
        <display value="MAJOR AFFECTIVE DISORDER 4" />
      </concept>
      <concept>
        <code value="OMIM:611252" />
        <display value="SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:611263" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 2 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:611274" />
        <display value="GLAUCOMA 1, OPEN ANGLE, N" />
      </concept>
      <concept>
        <code value="OMIM:611276" />
        <display value="GLAUCOMA 1, OPEN ANGLE, H" />
      </concept>
      <concept>
        <code value="OMIM:611277" />
        <display value="GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:611283" />
        <display value="ISOBUTYRYL-CoA DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:611284" />
        <display value="DYSTONIA, FOCAL, TASK-SPECIFIC" />
      </concept>
      <concept>
        <code value="OMIM:611291" />
        <display value="SEVERE COMBINED IMMUNODEFICIENCY WITH MICROCEPHALY, GROWTH RETARDATION, AND SENSITIVITY TO IONIZING RADIATION" />
      </concept>
      <concept>
        <code value="OMIM:611302" />
        <display value="SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:611307" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 12" />
      </concept>
      <concept>
        <code value="OMIM:611308" />
        <display value="PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:611363" />
        <display value="ATRIAL SEPTAL DEFECT 4" />
      </concept>
      <concept>
        <code value="OMIM:611364" />
        <display value="MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:611369" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:611376" />
        <display value="MUNGAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611377" />
        <display value="BRACHYDACTYLY, TYPE B2" />
      </concept>
      <concept>
        <code value="OMIM:611378" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 9" />
      </concept>
      <concept>
        <code value="OMIM:611381" />
        <display value="KALA-AZAR, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:611382" />
        <display value="KALA-AZAR, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:611383" />
        <display value="USHER SYNDROME, TYPE IID" />
      </concept>
      <concept>
        <code value="OMIM:611384" />
        <display value="PLASMODIUM FALCIPARUM FEVER EPISODES QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:611390" />
        <display value="SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:611391" />
        <display value="CATARACT 33, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:611403" />
        <display value="ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:611407" />
        <display value="CARDIOMYOPATHY, DILATED, 1W" />
      </concept>
      <concept>
        <code value="OMIM:611426" />
        <display value="TENTED EYEBROWS" />
      </concept>
      <concept>
        <code value="OMIM:611431" />
        <display value="LEGIUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611451" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 63" />
      </concept>
      <concept>
        <code value="OMIM:611456" />
        <display value="TREMOR, HEREDITARY ESSENTIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:611465" />
        <display value="GALLBLADDER DISEASE 4" />
      </concept>
      <concept>
        <code value="OMIM:611469" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:611488" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 10" />
      </concept>
      <concept>
        <code value="OMIM:611489" />
        <display value="CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:611490" />
        <display value="OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4" />
      </concept>
      <concept>
        <code value="OMIM:611493" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:611494" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:611497" />
        <display value="OSTEOPETROSIS, AUTOSOMAL RECESSIVE 6" />
      </concept>
      <concept>
        <code value="OMIM:611498" />
        <display value="NEPHRONOPHTHISIS 7" />
      </concept>
      <concept>
        <code value="OMIM:611515" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 7" />
      </concept>
      <concept>
        <code value="OMIM:611521" />
        <display value="IMMUNODEFICIENCY 35" />
      </concept>
      <concept>
        <code value="OMIM:611522" />
        <display value="INTRAOCULAR PRESSURE QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:611523" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:611528" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12" />
      </concept>
      <concept>
        <code value="OMIM:611535" />
        <display value="MAJOR AFFECTIVE DISORDER 5" />
      </concept>
      <concept>
        <code value="OMIM:611536" />
        <display value="MAJOR AFFECTIVE DISORDER 6" />
      </concept>
      <concept>
        <code value="OMIM:611543" />
        <display value="CAVITARY OPTIC DISC ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:611544" />
        <display value="CATARACT 17, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:611547" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 9" />
      </concept>
      <concept>
        <code value="OMIM:611548" />
        <display value="PREMATURE OVARIAN FAILURE 5" />
      </concept>
      <concept>
        <code value="OMIM:611553" />
        <display value="NOONAN SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:611554" />
        <display value="LEOPARD SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:611555" />
        <display value="RENAL TUBULAR ACIDOSIS, DISTAL, WITH NEPHROCALCINOSIS, SHORT STATURE, MENTAL RETARDATION, AND DISTINCTIVE FACIES" />
      </concept>
      <concept>
        <code value="OMIM:611556" />
        <display value="GLYCOGEN STORAGE DISEASE 0, MUSCLE" />
      </concept>
      <concept>
        <code value="OMIM:611560" />
        <display value="JOUBERT SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:611561" />
        <display value="MECKEL SYNDROME, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:611571" />
        <display value="OTOSCLEROSIS 4" />
      </concept>
      <concept>
        <code value="OMIM:611572" />
        <display value="OTOSCLEROSIS 7" />
      </concept>
      <concept>
        <code value="OMIM:611584" />
        <display value="WAARDENBURG SYNDROME, TYPE 2E" />
      </concept>
      <concept>
        <code value="OMIM:611588" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4" />
      </concept>
      <concept>
        <code value="OMIM:611590" />
        <display value="RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA" />
      </concept>
      <concept>
        <code value="OMIM:611597" />
        <display value="CATARACT 12, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:611598" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:611603" />
        <display value="LISSENCEPHALY 3" />
      </concept>
      <concept>
        <code value="OMIM:611615" />
        <display value="CARDIOMYOPATHY, DILATED, 1X" />
      </concept>
      <concept>
        <code value="OMIM:611630" />
        <display value="EPILEPSY, FAMILIAL TEMPORAL LOBE, 3" />
      </concept>
      <concept>
        <code value="OMIM:611631" />
        <display value="EPILEPSY, FAMILIAL TEMPORAL LOBE, 4" />
      </concept>
      <concept>
        <code value="OMIM:611634" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 9" />
      </concept>
      <concept>
        <code value="OMIM:611637" />
        <display value="PRIMARY LATERAL SCLEROSIS, ADULT, 1" />
      </concept>
      <concept>
        <code value="OMIM:611638" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5" />
      </concept>
      <concept>
        <code value="OMIM:611644" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:611650" />
        <display value="PERIPAPILLARY ATROPHY, BETA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:611664" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 7" />
      </concept>
      <concept>
        <code value="OMIM:611694" />
        <display value="DYSTONIA WITH CEREBELLAR ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:611702" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:611705" />
        <display value="SALIH MYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:611706" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12" />
      </concept>
      <concept>
        <code value="OMIM:611717" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH" />
      </concept>
      <concept>
        <code value="OMIM:611718" />
        <display value="HYPOMAGNESEMIA 4, RENAL" />
      </concept>
      <concept>
        <code value="OMIM:611719" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5" />
      </concept>
      <concept>
        <code value="OMIM:611721" />
        <display value="COMBINED SAPOSIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:611722" />
        <display value="KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:611724" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 8" />
      </concept>
      <concept>
        <code value="OMIM:611726" />
        <display value="EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS" />
      </concept>
      <concept>
        <code value="OMIM:611733" />
        <display value="DAUWERSE-PETERS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611738" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 7" />
      </concept>
      <concept>
        <code value="OMIM:611739" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 8" />
      </concept>
      <concept>
        <code value="OMIM:611742" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 9" />
      </concept>
      <concept>
        <code value="OMIM:611755" />
        <display value="LEBER CONGENITAL AMAUROSIS 10" />
      </concept>
      <concept>
        <code value="OMIM:611762" />
        <display value="FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:611771" />
        <display value="LIPOPROTEIN GLOMERULOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:611773" />
        <display value="ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS" />
      </concept>
      <concept>
        <code value="OMIM:611775" />
        <display value="KAWASAKI DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:611777" />
        <display value="BRUGADA SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:611783" />
        <display value="ERYTHROCYTOSIS, FAMILIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:611788" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 6" />
      </concept>
      <concept>
        <code value="OMIM:611804" />
        <display value="ELLIPTOCYTOSIS 1" />
      </concept>
      <concept>
        <code value="OMIM:611808" />
        <display value="TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS" />
      </concept>
      <concept>
        <code value="OMIM:611809" />
        <display value="BESTROPHINOPATHY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:611812" />
        <display value="46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS" />
      </concept>
      <concept>
        <code value="OMIM:611816" />
        <display value="TEMPLE-BARAITSER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611818" />
        <display value="LONG QT SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:611819" />
        <display value="LONG QT SYNDROME 10" />
      </concept>
      <concept>
        <code value="OMIM:611820" />
        <display value="LONG QT SYNDROME 11" />
      </concept>
      <concept>
        <code value="OMIM:611862" />
        <display value="WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:611863" />
        <display value="MICROTIA WITH NASOLACRIMAL DUCT IMPERFORATION AND EYE COLOBOMA" />
      </concept>
      <concept>
        <code value="OMIM:611867" />
        <display value="CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL" />
      </concept>
      <concept>
        <code value="OMIM:611868" />
        <display value="PROSTATE CANCER, HEREDITARY, 12" />
      </concept>
      <concept>
        <code value="OMIM:611875" />
        <display value="BRUGADA SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:611876" />
        <display value="BRUGADA SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:611878" />
        <display value="CARDIOMYOPATHY, DILATED, 1Y" />
      </concept>
      <concept>
        <code value="OMIM:611879" />
        <display value="CARDIOMYOPATHY, DILATED, 1Z" />
      </concept>
      <concept>
        <code value="OMIM:611880" />
        <display value="CARDIOMYOPATHY, DILATED, 2A" />
      </concept>
      <concept>
        <code value="OMIM:611881" />
        <display value="GLYCOGEN STORAGE DISEASE XII" />
      </concept>
      <concept>
        <code value="OMIM:611884" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 7" />
      </concept>
      <concept>
        <code value="OMIM:611886" />
        <display value="MESOMELIC DYSPLASIA, CAMERA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:611890" />
        <display value="LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:611891" />
        <display value="AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:611892" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 6" />
      </concept>
      <concept>
        <code value="OMIM:611895" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 9" />
      </concept>
      <concept>
        <code value="OMIM:611897" />
        <display value="NANOPHTHALMOS 3" />
      </concept>
      <concept>
        <code value="OMIM:611907" />
        <display value="EPISODIC ATAXIA, TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:611913" />
        <display value="CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB" />
      </concept>
      <concept>
        <code value="OMIM:611920" />
        <display value="C-REACTIVE PROTEIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:611926" />
        <display value="IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS" />
      </concept>
      <concept>
        <code value="OMIM:611928" />
        <display value="PROSTATE CANCER, HEREDITARY, 13" />
      </concept>
      <concept>
        <code value="OMIM:611929" />
        <display value="CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:611934" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:611936" />
        <display value="CHROMOSOME 3q29 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611938" />
        <display value="VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:611942" />
        <display value="EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:611943" />
        <display value="RIDDLE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611944" />
        <display value="LYMPHEDEMA, HEREDITARY, IB" />
      </concept>
      <concept>
        <code value="OMIM:611945" />
        <display value="SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:611953" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 11" />
      </concept>
      <concept>
        <code value="OMIM:611955" />
        <display value="PROSTATE CANCER, HEREDITARY, 11" />
      </concept>
      <concept>
        <code value="OMIM:611958" />
        <display value="PROSTATE CANCER, HEREDITARY, 14" />
      </concept>
      <concept>
        <code value="OMIM:611959" />
        <display value="PROSTATE CANCER, HEREDITARY, 15" />
      </concept>
      <concept>
        <code value="OMIM:611960" />
        <display value="ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:611961" />
        <display value="STEVENSON-CAREY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:611962" />
        <display value="HUNTER-MACDONALD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612001" />
        <display value="CHROMOSOME 15q13.3 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612004" />
        <display value="THROMBOCYTOPENIA 4" />
      </concept>
      <concept>
        <code value="OMIM:612005" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:612006" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:612007" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:612008" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 10" />
      </concept>
      <concept>
        <code value="OMIM:612009" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 11" />
      </concept>
      <concept>
        <code value="OMIM:612010" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 12" />
      </concept>
      <concept>
        <code value="OMIM:612011" />
        <display value="CELIAC DISEASE, SUSCEPTIBILITY TO, 13" />
      </concept>
      <concept>
        <code value="OMIM:612015" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE In" />
      </concept>
      <concept>
        <code value="OMIM:612016" />
        <display value="COENZYME Q10 DEFICIENCY, PRIMARY, 4" />
      </concept>
      <concept>
        <code value="OMIM:612017" />
        <display value="PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:612018" />
        <display value="CATARACT 47" />
      </concept>
      <concept>
        <code value="OMIM:612020" />
        <display value="SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612030" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:612042" />
        <display value="RECOMBINATION RATE QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612052" />
        <display value="SMOKING AS A QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:612067" />
        <display value="DYSTONIA 16" />
      </concept>
      <concept>
        <code value="OMIM:612069" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:612073" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)" />
      </concept>
      <concept>
        <code value="OMIM:612075" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)" />
      </concept>
      <concept>
        <code value="OMIM:612076" />
        <display value="HYPOURICEMIA, RENAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:612079" />
        <display value="ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612083" />
        <display value="MUSCLE STRENGTH QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612089" />
        <display value="HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM" />
      </concept>
      <concept>
        <code value="OMIM:612095" />
        <display value="RETINITIS PIGMENTOSA 41" />
      </concept>
      <concept>
        <code value="OMIM:612096" />
        <display value="OTOSCLEROSIS 8" />
      </concept>
      <concept>
        <code value="OMIM:612097" />
        <display value="DEAFNESS, UNILATERAL, WITH DELAYED ENDOLYMPHATIC HYDROPS" />
      </concept>
      <concept>
        <code value="OMIM:612098" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11" />
      </concept>
      <concept>
        <code value="OMIM:612099" />
        <display value="TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:612100" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 15" />
      </concept>
      <concept>
        <code value="OMIM:612108" />
        <display value="FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612109" />
        <display value="OCULOAURICULAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612110" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 9" />
      </concept>
      <concept>
        <code value="OMIM:612113" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 10" />
      </concept>
      <concept>
        <code value="OMIM:612114" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 11" />
      </concept>
      <concept>
        <code value="OMIM:612119" />
        <display value="TREHALASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:612124" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12" />
      </concept>
      <concept>
        <code value="OMIM:612126" />
        <display value="GLUT1 DEFICIENCY SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:612132" />
        <display value="ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 2" />
      </concept>
      <concept>
        <code value="OMIM:612138" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA" />
      </concept>
      <concept>
        <code value="OMIM:612158" />
        <display value="CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION" />
      </concept>
      <concept>
        <code value="OMIM:612160" />
        <display value="HISTIOCYTOMA, ANGIOMATOID FIBROUS" />
      </concept>
      <concept>
        <code value="OMIM:612161" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 7" />
      </concept>
      <concept>
        <code value="OMIM:612162" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 8" />
      </concept>
      <concept>
        <code value="OMIM:612164" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4" />
      </concept>
      <concept>
        <code value="OMIM:612165" />
        <display value="RETINITIS PIGMENTOSA 29" />
      </concept>
      <concept>
        <code value="OMIM:612198" />
        <display value="DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA" />
      </concept>
      <concept>
        <code value="OMIM:612199" />
        <display value="CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 1" />
      </concept>
      <concept>
        <code value="OMIM:612201" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:612219" />
        <display value="EWING SARCOMA" />
      </concept>
      <concept>
        <code value="OMIM:612221" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 10" />
      </concept>
      <concept>
        <code value="OMIM:612223" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 11" />
      </concept>
      <concept>
        <code value="OMIM:612224" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 12" />
      </concept>
      <concept>
        <code value="OMIM:612225" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9" />
      </concept>
      <concept>
        <code value="OMIM:612226" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 13" />
      </concept>
      <concept>
        <code value="OMIM:612227" />
        <display value="DIABETES MELLITUS, KETOSIS-PRONE" />
      </concept>
      <concept>
        <code value="OMIM:612228" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 14" />
      </concept>
      <concept>
        <code value="OMIM:612229" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:612230" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:612231" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:612232" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:612233" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 4" />
      </concept>
      <concept>
        <code value="OMIM:612237" />
        <display value="CHONDROSARCOMA, EXTRASKELETAL MYXOID" />
      </concept>
      <concept>
        <code value="OMIM:612238" />
        <display value="SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:612239" />
        <display value="SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:612240" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 7" />
      </concept>
      <concept>
        <code value="OMIM:612241" />
        <display value="INFLAMMATORY BOWEL DISEASE 12" />
      </concept>
      <concept>
        <code value="OMIM:612242" />
        <display value="CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612244" />
        <display value="INFLAMMATORY BOWEL DISEASE 13" />
      </concept>
      <concept>
        <code value="OMIM:612245" />
        <display value="INFLAMMATORY BOWEL DISEASE 14" />
      </concept>
      <concept>
        <code value="OMIM:612247" />
        <display value="CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS" />
      </concept>
      <concept>
        <code value="OMIM:612251" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 10" />
      </concept>
      <concept>
        <code value="OMIM:612253" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11" />
      </concept>
      <concept>
        <code value="OMIM:612254" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 12" />
      </concept>
      <concept>
        <code value="OMIM:612255" />
        <display value="INFLAMMATORY BOWEL DISEASE 15" />
      </concept>
      <concept>
        <code value="OMIM:612259" />
        <display value="INFLAMMATORY BOWEL DISEASE 16" />
      </concept>
      <concept>
        <code value="OMIM:612260" />
        <display value="MYD88 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:612261" />
        <display value="INFLAMMATORY BOWEL DISEASE 17" />
      </concept>
      <concept>
        <code value="OMIM:612262" />
        <display value="INFLAMMATORY BOWEL DISEASE 18" />
      </concept>
      <concept>
        <code value="OMIM:612263" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:612267" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 10" />
      </concept>
      <concept>
        <code value="OMIM:612269" />
        <display value="EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:612271" />
        <display value="SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 11" />
      </concept>
      <concept>
        <code value="OMIM:612274" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 8" />
      </concept>
      <concept>
        <code value="OMIM:612278" />
        <display value="INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 19" />
      </concept>
      <concept>
        <code value="OMIM:612279" />
        <display value="GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:612281" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6" />
      </concept>
      <concept>
        <code value="OMIM:612284" />
        <display value="MECKEL SYNDROME, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:612285" />
        <display value="JOUBERT SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:612286" />
        <display value="NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1" />
      </concept>
      <concept>
        <code value="OMIM:612287" />
        <display value="NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:612288" />
        <display value="INFLAMMATORY BOWEL DISEASE 20" />
      </concept>
      <concept>
        <code value="OMIM:612289" />
        <display value="FONTAINE PROGEROID SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612290" />
        <display value="MICROTIA, HEARING IMPAIRMENT, AND CLEFT PALATE" />
      </concept>
      <concept>
        <code value="OMIM:612291" />
        <display value="JOUBERT SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:612292" />
        <display value="BIRK-BAREL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612293" />
        <display value="POROKERATOSIS 5, DISSEMINATED SUPERFICIAL ACTINIC TYPE" />
      </concept>
      <concept>
        <code value="OMIM:612300" />
        <display value="HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:612301" />
        <display value="OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7" />
      </concept>
      <concept>
        <code value="OMIM:612304" />
        <display value="THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612306" />
        <display value="THYROID-STIMULATING HORMONE LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612310" />
        <display value="PREMATURE OVARIAN FAILURE 6" />
      </concept>
      <concept>
        <code value="OMIM:612311" />
        <display value="ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:612312" />
        <display value="ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:612313" />
        <display value="GLASS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612318" />
        <display value="PSEUDOFOLLICULITIS BARBAE" />
      </concept>
      <concept>
        <code value="OMIM:612319" />
        <display value="SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612335" />
        <display value="SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:612336" />
        <display value="THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:612337" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 22" />
      </concept>
      <concept>
        <code value="OMIM:612343" />
        <display value="MUSICAL APTITUDE QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:612345" />
        <display value="CHROMOSOME 2q31.2 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612347" />
        <display value="JERVELL AND LANGE-NIELSEN SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:612348" />
        <display value="THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR" />
      </concept>
      <concept>
        <code value="OMIM:612350" />
        <display value="EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 3" />
      </concept>
      <concept>
        <code value="OMIM:612353" />
        <display value="POROKERATOSIS 6, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:612354" />
        <display value="INFLAMMATORY BOWEL DISEASE 21" />
      </concept>
      <concept>
        <code value="OMIM:612356" />
        <display value="HEPARIN COFACTOR II DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:612357" />
        <display value="MAJOR AFFECTIVE DISORDER 8" />
      </concept>
      <concept>
        <code value="OMIM:612361" />
        <display value="SCHIZOPHRENIA 14" />
      </concept>
      <concept>
        <code value="OMIM:612362" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12" />
      </concept>
      <concept>
        <code value="OMIM:612363" />
        <display value="ALANINE AMINOTRANSFERASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612364" />
        <display value="ALANINE AMINOTRANSFERASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:612365" />
        <display value="GAMMA GLUTAMYLTRANSFERASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612366" />
        <display value="GAMMA GLUTAMYLTRANSFERASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:612367" />
        <display value="ALKALINE PHOSPHATASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:612368" />
        <display value="ALKALINE PHOSPHATASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:612369" />
        <display value="ALKALINE PHOSPHATASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:612370" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:612371" />
        <display value="MAJOR AFFECTIVE DISORDER 7" />
      </concept>
      <concept>
        <code value="OMIM:612372" />
        <display value="MAJOR AFFECTIVE DISORDER 9" />
      </concept>
      <concept>
        <code value="OMIM:612376" />
        <display value="ACUTE PROMYELOCYTIC LEUKEMIA" />
      </concept>
      <concept>
        <code value="OMIM:612378" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 13" />
      </concept>
      <concept>
        <code value="OMIM:612379" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq" />
      </concept>
      <concept>
        <code value="OMIM:612380" />
        <display value="INFLAMMATORY BOWEL DISEASE 22" />
      </concept>
      <concept>
        <code value="OMIM:612381" />
        <display value="INFLAMMATORY BOWEL DISEASE 23" />
      </concept>
      <concept>
        <code value="OMIM:612387" />
        <display value="SARCOIDOSIS, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:612388" />
        <display value="SARCOIDOSIS, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:612389" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 2B" />
      </concept>
      <concept>
        <code value="OMIM:612390" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 2C" />
      </concept>
      <concept>
        <code value="OMIM:612394" />
        <display value="BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:612396" />
        <display value="ALLANTOICASE" />
      </concept>
      <concept>
        <code value="OMIM:612400" />
        <display value="OSTEOARTHRITIS SUSCEPTIBILITY 5" />
      </concept>
      <concept>
        <code value="OMIM:612401" />
        <display value="OSTEOARTHRITIS SUSCEPTIBILITY 6" />
      </concept>
      <concept>
        <code value="OMIM:612406" />
        <display value="DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612410" />
        <display value="PSORIASIS 10, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:612416" />
        <display value="FACTOR XI DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:612417" />
        <display value="NARCOLEPSY 4, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:612421" />
        <display value="ALOPECIA, ANDROGENETIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:612422" />
        <display value="CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3" />
      </concept>
      <concept>
        <code value="OMIM:612423" />
        <display value="PREKALLIKREIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:612431" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 27" />
      </concept>
      <concept>
        <code value="OMIM:612433" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 45" />
      </concept>
      <concept>
        <code value="OMIM:612437" />
        <display value="EPILEPSY, PROGRESSIVE MYOCLONIC, 1B" />
      </concept>
      <concept>
        <code value="OMIM:612438" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 6" />
      </concept>
      <concept>
        <code value="OMIM:612444" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 9" />
      </concept>
      <concept>
        <code value="OMIM:612445" />
        <display value="SCOLIOSIS, ARACHNODACTYLY, AND BLINDNESS" />
      </concept>
      <concept>
        <code value="OMIM:612446" />
        <display value="COMPLEMENT COMPONENT 6 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:612447" />
        <display value="SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:612448" />
        <display value="AGE-RELATED HEARING IMPAIRMENT 1" />
      </concept>
      <concept>
        <code value="OMIM:612459" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13" />
      </concept>
      <concept>
        <code value="OMIM:612460" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14" />
      </concept>
      <concept>
        <code value="OMIM:612462" />
        <display value="PSEUDOHYPOPARATHYROIDISM, TYPE IC" />
      </concept>
      <concept>
        <code value="OMIM:612463" />
        <display value="PSEUDOPSEUDOHYPOPARATHYROIDISM" />
      </concept>
      <concept>
        <code value="OMIM:612469" />
        <display value="WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, MENTAL RETARDATION, AND OBESITY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612474" />
        <display value="CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB" />
      </concept>
      <concept>
        <code value="OMIM:612475" />
        <display value="CHROMOSOME 1q21.1 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612513" />
        <display value="CHROMOSOME 2p16.1-p15 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612514" />
        <display value="SPECIFIC LANGUAGE IMPAIRMENT 4" />
      </concept>
      <concept>
        <code value="OMIM:612518" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 10" />
      </concept>
      <concept>
        <code value="OMIM:612520" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 20" />
      </concept>
      <concept>
        <code value="OMIM:612521" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 21" />
      </concept>
      <concept>
        <code value="OMIM:612522" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 22" />
      </concept>
      <concept>
        <code value="OMIM:612525" />
        <display value="PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 5" />
      </concept>
      <concept>
        <code value="OMIM:612526" />
        <display value="LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:612527" />
        <display value="DIAMOND-BLACKFAN ANEMIA 4" />
      </concept>
      <concept>
        <code value="OMIM:612528" />
        <display value="DIAMOND-BLACKFAN ANEMIA 5" />
      </concept>
      <concept>
        <code value="OMIM:612529" />
        <display value="AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2" />
      </concept>
      <concept>
        <code value="OMIM:612530" />
        <display value="CHROMOSOME 1q41-q42 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612539" />
        <display value="SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:612540" />
        <display value="MYOPATHY, CONGENITAL, COMPTON-NORTH" />
      </concept>
      <concept>
        <code value="OMIM:612541" />
        <display value="NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612542" />
        <display value="VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612551" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:612554" />
        <display value="MYOPIA 16, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:612555" />
        <display value="BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:612556" />
        <display value="ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612557" />
        <display value="LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:612558" />
        <display value="LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:612559" />
        <display value="LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:612560" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 12" />
      </concept>
      <concept>
        <code value="OMIM:612561" />
        <display value="DIAMOND-BLACKFAN ANEMIA 6" />
      </concept>
      <concept>
        <code value="OMIM:612562" />
        <display value="DIAMOND-BLACKFAN ANEMIA 7" />
      </concept>
      <concept>
        <code value="OMIM:612563" />
        <display value="DIAMOND-BLACKFAN ANEMIA 8" />
      </concept>
      <concept>
        <code value="OMIM:612566" />
        <display value="INFLAMMATORY BOWEL DISEASE 24" />
      </concept>
      <concept>
        <code value="OMIM:612567" />
        <display value="INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612571" />
        <display value="LUNG CANCER SUSCEPTIBILITY 3" />
      </concept>
      <concept>
        <code value="OMIM:612572" />
        <display value="RETINITIS PIGMENTOSA 46" />
      </concept>
      <concept>
        <code value="OMIM:612573" />
        <display value="MEAN PLATELET VOLUME QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612574" />
        <display value="MEAN PLATELET VOLUME QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:612575" />
        <display value="MEAN PLATELET VOLUME QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:612576" />
        <display value="CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612577" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 11" />
      </concept>
      <concept>
        <code value="OMIM:612578" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 15" />
      </concept>
      <concept>
        <code value="OMIM:612579" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 16" />
      </concept>
      <concept>
        <code value="OMIM:612580" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 3" />
      </concept>
      <concept>
        <code value="OMIM:612581" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 4" />
      </concept>
      <concept>
        <code value="OMIM:612582" />
        <display value="CHROMOSOME 6pter-p24 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612586" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 9" />
      </concept>
      <concept>
        <code value="OMIM:612587" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 10" />
      </concept>
      <concept>
        <code value="OMIM:612589" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:612590" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:612591" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 10" />
      </concept>
      <concept>
        <code value="OMIM:612592" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 11" />
      </concept>
      <concept>
        <code value="OMIM:612593" />
        <display value="LUNG CANCER SUSCEPTIBILITY 4" />
      </concept>
      <concept>
        <code value="OMIM:612594" />
        <display value="MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:612595" />
        <display value="MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:612596" />
        <display value="MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:612599" />
        <display value="PSORIASIS 11, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:612621" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 5" />
      </concept>
      <concept>
        <code value="OMIM:612622" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 23" />
      </concept>
      <concept>
        <code value="OMIM:612623" />
        <display value="MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:612624" />
        <display value="MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:612626" />
        <display value="CHROMOSOME 15q26-qter DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612627" />
        <display value="SEIZURES, BENIGN FAMILIAL INFANTILE, 4" />
      </concept>
      <concept>
        <code value="OMIM:612628" />
        <display value="MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:612629" />
        <display value="ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:612630" />
        <display value="HAIR MORPHOLOGY 1" />
      </concept>
      <concept>
        <code value="OMIM:612631" />
        <display value="ADENYLATE KINASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:612632" />
        <display value="USHER SYNDROME, TYPE IH" />
      </concept>
      <concept>
        <code value="OMIM:612633" />
        <display value="MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:612634" />
        <display value="MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:612635" />
        <display value="MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:612637" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 10" />
      </concept>
      <concept>
        <code value="OMIM:612639" />
        <display value="INFLAMMATORY BOWEL DISEASE 26" />
      </concept>
      <concept>
        <code value="OMIM:612642" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 59" />
      </concept>
      <concept>
        <code value="OMIM:612643" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 3B" />
      </concept>
      <concept>
        <code value="OMIM:612644" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 2B" />
      </concept>
      <concept>
        <code value="OMIM:612645" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 1B" />
      </concept>
      <concept>
        <code value="OMIM:612649" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 11" />
      </concept>
      <concept>
        <code value="OMIM:612650" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 12" />
      </concept>
      <concept>
        <code value="OMIM:612651" />
        <display value="ENDOCRINE-CEREBROOSTEODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:612653" />
        <display value="SPHEROCYTOSIS, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:612656" />
        <display value="EPISODIC ATAXIA, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:612657" />
        <display value="CONE-ROD DYSTROPHY 12" />
      </concept>
      <concept>
        <code value="OMIM:612671" />
        <display value="URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:612674" />
        <display value="POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT" />
      </concept>
      <concept>
        <code value="OMIM:612690" />
        <display value="SPHEROCYTOSIS, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:612691" />
        <display value="POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL" />
      </concept>
      <concept>
        <code value="OMIM:612692" />
        <display value="AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612702" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:612703" />
        <display value="MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612712" />
        <display value="LEBER CONGENITAL AMAUROSIS 13" />
      </concept>
      <concept>
        <code value="OMIM:612713" />
        <display value="KAHRIZI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612714" />
        <display value="EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIAL HYPEROSTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:612715" />
        <display value="DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 2" />
      </concept>
      <concept>
        <code value="OMIM:612716" />
        <display value="DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:612717" />
        <display value="MYOPIA 15, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:612718" />
        <display value="CEREBRAL CREATINE DEFICIENCY SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:612726" />
        <display value="HARDIKAR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612727" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 13" />
      </concept>
      <concept>
        <code value="OMIM:612728" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 14" />
      </concept>
      <concept>
        <code value="OMIM:612729" />
        <display value="LEAN BODY MASS QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612731" />
        <display value="FACIOCARDIOMELIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612736" />
        <display value="CEREBRAL CREATINE DEFICIENCY SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:612737" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 17" />
      </concept>
      <concept>
        <code value="OMIM:612740" />
        <display value="PORPHYRIA, ACUTE HEPATIC" />
      </concept>
      <concept>
        <code value="OMIM:612759" />
        <display value="SYNESTHESIA" />
      </concept>
      <concept>
        <code value="OMIM:612775" />
        <display value="CONE-ROD DYSTROPHY 9" />
      </concept>
      <concept>
        <code value="OMIM:612776" />
        <display value="HYPOGLOSSIA WITH SITUS INVERSUS" />
      </concept>
      <concept>
        <code value="OMIM:612777" />
        <display value="HYPOTONIA, SEIZURES, AND PRECOCIOUS PUBERTY" />
      </concept>
      <concept>
        <code value="OMIM:612780" />
        <display value="SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE" />
      </concept>
      <concept>
        <code value="OMIM:612781" />
        <display value="ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IB" />
      </concept>
      <concept>
        <code value="OMIM:612782" />
        <display value="IMMUNODEFICIENCY 9" />
      </concept>
      <concept>
        <code value="OMIM:612783" />
        <display value="IMMUNODEFICIENCY 10" />
      </concept>
      <concept>
        <code value="OMIM:612785" />
        <display value="MEGARBANE-JALKH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612789" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 71" />
      </concept>
      <concept>
        <code value="OMIM:612794" />
        <display value="ATRIAL SEPTAL DEFECT 5" />
      </concept>
      <concept>
        <code value="OMIM:612795" />
        <display value="POLYUNSATURATED FATTY ACIDS PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612796" />
        <display value="INFLAMMATORY BOWEL DISEASE 27" />
      </concept>
      <concept>
        <code value="OMIM:612797" />
        <display value="HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12" />
      </concept>
      <concept>
        <code value="OMIM:612798" />
        <display value="QUESTION MARK EARS, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:612813" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE" />
      </concept>
      <concept>
        <code value="OMIM:612838" />
        <display value="BRUGADA SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:612840" />
        <display value="LEUKOCYTE ADHESION DEFICIENCY, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:612841" />
        <display value="HYPOTRICHOSIS 5" />
      </concept>
      <concept>
        <code value="OMIM:612843" />
        <display value="KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:612847" />
        <display value="BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES" />
      </concept>
      <concept>
        <code value="OMIM:612851" />
        <display value="NARCOLEPSY 5, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:612852" />
        <display value="OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS" />
      </concept>
      <concept>
        <code value="OMIM:612853" />
        <display value="RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:612858" />
        <display value="OROFACIAL CLEFT 12" />
      </concept>
      <concept>
        <code value="OMIM:612862" />
        <display value="PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:612863" />
        <display value="CHROMOSOME 6q24-q25 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612867" />
        <display value="CORNEAL DYSTROPHY, SUBEPITHELIAL MUCINOUS" />
      </concept>
      <concept>
        <code value="OMIM:612868" />
        <display value="CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS" />
      </concept>
      <concept>
        <code value="OMIM:612874" />
        <display value="ERYTHROCYTE AMP DEAMINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:612875" />
        <display value="GONADOTROPIN-RELEASING HORMONE RECEPTOR 2" />
      </concept>
      <concept>
        <code value="OMIM:612876" />
        <display value="SPINOCEREBELLAR ATAXIA 9" />
      </concept>
      <concept>
        <code value="OMIM:612877" />
        <display value="CARDIOMYOPATHY, DILATED, 1BB" />
      </concept>
      <concept>
        <code value="OMIM:612881" />
        <display value="CHROMOSOME 5q14.3 DELETION SYNDROME, DISTAL" />
      </concept>
      <concept>
        <code value="OMIM:612882" />
        <display value="MENARCHE, AGE AT, QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:612883" />
        <display value="MENARCHE, AGE AT, QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:612884" />
        <display value="MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:612885" />
        <display value="PREMATURE OVARIAN FAILURE 10" />
      </concept>
      <concept>
        <code value="OMIM:612886" />
        <display value="MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:612892" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 18" />
      </concept>
      <concept>
        <code value="OMIM:612893" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 19" />
      </concept>
      <concept>
        <code value="OMIM:612894" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 20" />
      </concept>
      <concept>
        <code value="OMIM:612899" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:612900" />
        <display value="CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:612908" />
        <display value="KERATOSIS PALMOPLANTARIS STRIATA II" />
      </concept>
      <concept>
        <code value="OMIM:612913" />
        <display value="OROFACIODIGITAL SYNDROME XI" />
      </concept>
      <concept>
        <code value="OMIM:612916" />
        <display value="ZECHI-CEIDE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612917" />
        <display value="GIACHETI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612918" />
        <display value="CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI" />
      </concept>
      <concept>
        <code value="OMIM:612921" />
        <display value="THREE M SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:612922" />
        <display value="HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:612923" />
        <display value="HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:612924" />
        <display value="HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:612925" />
        <display value="HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:612926" />
        <display value="HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:612929" />
        <display value="MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:612932" />
        <display value="GLYCOGEN STORAGE DISEASE XIII" />
      </concept>
      <concept>
        <code value="OMIM:612933" />
        <display value="GLYCOGEN STORAGE DISEASE XI" />
      </concept>
      <concept>
        <code value="OMIM:612936" />
        <display value="SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612937" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15" />
      </concept>
      <concept>
        <code value="OMIM:612938" />
        <display value="GROWTH RETARDATION, DEVELOPMENTAL DELAY, AND FACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:612940" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB" />
      </concept>
      <concept>
        <code value="OMIM:612943" />
        <display value="RETINITIS PIGMENTOSA 42" />
      </concept>
      <concept>
        <code value="OMIM:612946" />
        <display value="HADZISELIMOVIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:612947" />
        <display value="MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE" />
      </concept>
      <concept>
        <code value="OMIM:612948" />
        <display value="STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, MENTAL RETARDATION, AND DYSMORPHIC FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:612949" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39" />
      </concept>
      <concept>
        <code value="OMIM:612950" />
        <display value="PSORIASIS 12, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:612951" />
        <display value="LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:612952" />
        <display value="AICARDI-GOUTIERES SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:612953" />
        <display value="PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:612954" />
        <display value="MYOPATHY, MYOFIBRILLAR, 6" />
      </concept>
      <concept>
        <code value="OMIM:612955" />
        <display value="LONG QT SYNDROME 12" />
      </concept>
      <concept>
        <code value="OMIM:612956" />
        <display value="VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:612957" />
        <display value="VITAMIN B6 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:612961" />
        <display value="MULTIPLE SYNOSTOSES SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:612964" />
        <display value="PREMATURE OVARIAN FAILURE 7" />
      </concept>
      <concept>
        <code value="OMIM:612965" />
        <display value="46,XY SEX REVERSAL 3" />
      </concept>
      <concept>
        <code value="OMIM:612967" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 15" />
      </concept>
      <concept>
        <code value="OMIM:612968" />
        <display value="CATARACT 34, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:612970" />
        <display value="NEUROBLASTOMA BREAKPOINT FAMILY, MEMBER 17, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:612975" />
        <display value="SHORT SLEEPER" />
      </concept>
      <concept>
        <code value="OMIM:612976" />
        <display value="AGE-RELATED HEARING IMPAIRMENT 2" />
      </concept>
      <concept>
        <code value="OMIM:612989" />
        <display value="OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:612997" />
        <display value="SPERMATOGENIC FAILURE 7" />
      </concept>
      <concept>
        <code value="OMIM:612998" />
        <display value="EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:612999" />
        <display value="EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:613000" />
        <display value="PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 1" />
      </concept>
      <concept>
        <code value="OMIM:613001" />
        <display value="ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:613002" />
        <display value="ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613003" />
        <display value="ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:613005" />
        <display value="SANTOS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613006" />
        <display value="DIABETES MELLITUS, INSULIN-DEPENDENT, 24" />
      </concept>
      <concept>
        <code value="OMIM:613007" />
        <display value="BILIARY CIRRHOSIS, PRIMARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:613008" />
        <display value="BILIARY CIRRHOSIS, PRIMARY, 3" />
      </concept>
      <concept>
        <code value="OMIM:613011" />
        <display value="LYMPHOPROLIFERATIVE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:613013" />
        <display value="NEUROBLASTOMA, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613014" />
        <display value="NEUROBLASTOMA, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:613015" />
        <display value="NEUROBLASTOMA, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:613016" />
        <display value="NEUROBLASTOMA, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:613017" />
        <display value="NEUROBLASTOMA, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:613021" />
        <display value="BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2" />
      </concept>
      <concept>
        <code value="OMIM:613024" />
        <display value="FOLLICULAR LYMPHOMA, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:613025" />
        <display value="SCHIZOPHRENIA 13" />
      </concept>
      <concept>
        <code value="OMIM:613026" />
        <display value="CHROMOSOME 19q13.11 DELETION SYNDROME, DISTAL" />
      </concept>
      <concept>
        <code value="OMIM:613027" />
        <display value="GLYCOGEN STORAGE DISEASE IXc" />
      </concept>
      <concept>
        <code value="OMIM:613028" />
        <display value="GLIOMA SUSCEPTIBILITY 2" />
      </concept>
      <concept>
        <code value="OMIM:613029" />
        <display value="GLIOMA SUSCEPTIBILITY 3" />
      </concept>
      <concept>
        <code value="OMIM:613030" />
        <display value="GLIOMA SUSCEPTIBILITY 5" />
      </concept>
      <concept>
        <code value="OMIM:613031" />
        <display value="GLIOMA SUSCEPTIBILITY 6" />
      </concept>
      <concept>
        <code value="OMIM:613032" />
        <display value="GLIOMA SUSCEPTIBILITY 7" />
      </concept>
      <concept>
        <code value="OMIM:613033" />
        <display value="GLIOMA SUSCEPTIBILITY 8" />
      </concept>
      <concept>
        <code value="OMIM:613035" />
        <display value="HEARING LOSS, NOISE-INDUCED, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:613038" />
        <display value="PITUITARY HORMONE DEFICIENCY, COMBINED, 1" />
      </concept>
      <concept>
        <code value="OMIM:613055" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 8" />
      </concept>
      <concept>
        <code value="OMIM:613058" />
        <display value="BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613059" />
        <display value="BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:613060" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10" />
      </concept>
      <concept>
        <code value="OMIM:613061" />
        <display value="BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:613062" />
        <display value="BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:613063" />
        <display value="BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:613064" />
        <display value="DERMATITIS, ATOPIC, 7" />
      </concept>
      <concept>
        <code value="OMIM:613065" />
        <display value="LEUKEMIA, ACUTE LYMPHOBLASTIC" />
      </concept>
      <concept>
        <code value="OMIM:613067" />
        <display value="LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613068" />
        <display value="NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613070" />
        <display value="LIVER FAILURE, INFANTILE, TRANSIENT" />
      </concept>
      <concept>
        <code value="OMIM:613071" />
        <display value="BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3" />
      </concept>
      <concept>
        <code value="OMIM:613073" />
        <display value="METAPHYSEAL ANADYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:613074" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 50" />
      </concept>
      <concept>
        <code value="OMIM:613075" />
        <display value="MACS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613076" />
        <display value="MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARING LOSS, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:613077" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5" />
      </concept>
      <concept>
        <code value="OMIM:613078" />
        <display value="NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:613079" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 77" />
      </concept>
      <concept>
        <code value="OMIM:613080" />
        <display value="46,XY SEX REVERSAL 5" />
      </concept>
      <concept>
        <code value="OMIM:613085" />
        <display value="GLAUCOMA 3, PRIMARY CONGENITAL, C" />
      </concept>
      <concept>
        <code value="OMIM:613086" />
        <display value="GLAUCOMA 3, PRIMARY CONGENITAL, D" />
      </concept>
      <concept>
        <code value="OMIM:613087" />
        <display value="ATRIAL SEPTAL DEFECT 6" />
      </concept>
      <concept>
        <code value="OMIM:613088" />
        <display value="PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613089" />
        <display value="CAPILLARY MALFORMATION OF THE LOWER LIP, LYMPHATIC MALFORMATION OF FACE AND NECK, ASYMMETRY OF FACE AND LIMBS, AND PARTIAL/GENERALIZED OVERGROWTH" />
      </concept>
      <concept>
        <code value="OMIM:613090" />
        <display value="BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:613091" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:613092" />
        <display value="HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2" />
      </concept>
      <concept>
        <code value="OMIM:613093" />
        <display value="CONE DYSTROPHY 4" />
      </concept>
      <concept>
        <code value="OMIM:613094" />
        <display value="MICROPHTHALMIA, ISOLATED 4" />
      </concept>
      <concept>
        <code value="OMIM:613095" />
        <display value="POLYCYSTIC KIDNEY DISEASE 2 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:613096" />
        <display value="SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:613098" />
        <display value="INCREASED ANALGESIA FROM KAPPA-OPIOID RECEPTOR AGONIST, FEMALE-SPECIFIC" />
      </concept>
      <concept>
        <code value="OMIM:613099" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:613100" />
        <display value="GLAUCOMA 1, OPEN ANGLE, O" />
      </concept>
      <concept>
        <code value="OMIM:613101" />
        <display value="HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:613102" />
        <display value="HYPOTRICHOSIS AND RECURRENT SKIN VESICLES" />
      </concept>
      <concept>
        <code value="OMIM:613105" />
        <display value="CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2" />
      </concept>
      <concept>
        <code value="OMIM:613106" />
        <display value="VERTIGO, BENIGN RECURRENT, 2" />
      </concept>
      <concept>
        <code value="OMIM:613107" />
        <display value="NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:613108" />
        <display value="CANDIDIASIS, FAMILIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:613112" />
        <display value="MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:613115" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB" />
      </concept>
      <concept>
        <code value="OMIM:613116" />
        <display value="THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613118" />
        <display value="ANTITHROMBIN III DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613119" />
        <display value="BRUGADA SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:613120" />
        <display value="BRUGADA SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:613122" />
        <display value="CARDIOMYOPATHY, DILATED, 1CC" />
      </concept>
      <concept>
        <code value="OMIM:613123" />
        <display value="BRUGADA SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:613124" />
        <display value="HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:613135" />
        <display value="PARKINSONISM-DYSTONIA, INFANTILE, 1" />
      </concept>
      <concept>
        <code value="OMIM:613144" />
        <display value="CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, 3" />
      </concept>
      <concept>
        <code value="OMIM:613145" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 14" />
      </concept>
      <concept>
        <code value="OMIM:613148" />
        <display value="INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613150" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2" />
      </concept>
      <concept>
        <code value="OMIM:613151" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3" />
      </concept>
      <concept>
        <code value="OMIM:613152" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4" />
      </concept>
      <concept>
        <code value="OMIM:613153" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5" />
      </concept>
      <concept>
        <code value="OMIM:613154" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6" />
      </concept>
      <concept>
        <code value="OMIM:613155" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1" />
      </concept>
      <concept>
        <code value="OMIM:613156" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2" />
      </concept>
      <concept>
        <code value="OMIM:613157" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3" />
      </concept>
      <concept>
        <code value="OMIM:613158" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2" />
      </concept>
      <concept>
        <code value="OMIM:613159" />
        <display value="NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1" />
      </concept>
      <concept>
        <code value="OMIM:613161" />
        <display value="BETA-UREIDOPROPIONASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613162" />
        <display value="SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613163" />
        <display value="GABA-TRANSAMINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613164" />
        <display value="PARKINSON DISEASE 16" />
      </concept>
      <concept>
        <code value="OMIM:613172" />
        <display value="CARDIOMYOPATHY, DILATED, 1DD" />
      </concept>
      <concept>
        <code value="OMIM:613174" />
        <display value="CHROMOSOME 5p13 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613177" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC" />
      </concept>
      <concept>
        <code value="OMIM:613179" />
        <display value="PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613180" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 8" />
      </concept>
      <concept>
        <code value="OMIM:613192" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13" />
      </concept>
      <concept>
        <code value="OMIM:613193" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 13" />
      </concept>
      <concept>
        <code value="OMIM:613194" />
        <display value="RETINITIS PIGMENTOSA 50" />
      </concept>
      <concept>
        <code value="OMIM:613195" />
        <display value="WEILL-MARCHESANI SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:613204" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613205" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:613206" />
        <display value="SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613207" />
        <display value="ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:613211" />
        <display value="AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3" />
      </concept>
      <concept>
        <code value="OMIM:613215" />
        <display value="CHROMOSOME 17p13.3, CENTROMERIC, DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613216" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C" />
      </concept>
      <concept>
        <code value="OMIM:613217" />
        <display value="DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:613219" />
        <display value="FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:613223" />
        <display value="LEPROSY, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:613224" />
        <display value="NOONAN SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:613225" />
        <display value="FACTOR XIII, A SUBUNIT, DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:613227" />
        <display value="CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:613229" />
        <display value="TRICHOTILLOMANIA" />
      </concept>
      <concept>
        <code value="OMIM:613233" />
        <display value="FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:613235" />
        <display value="FACTOR XIII, B SUBUNIT, DEFICIENCY OF" />
      </concept>
      <concept>
        <code value="OMIM:613237" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5" />
      </concept>
      <concept>
        <code value="OMIM:613238" />
        <display value="SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:613239" />
        <display value="THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613241" />
        <display value="PSEUDOPILI ANNULATI" />
      </concept>
      <concept>
        <code value="OMIM:613243" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13" />
      </concept>
      <concept>
        <code value="OMIM:613244" />
        <display value="COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8" />
      </concept>
      <concept>
        <code value="OMIM:613251" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14" />
      </concept>
      <concept>
        <code value="OMIM:613252" />
        <display value="CARDIOMYOPATHY, DILATED, 1EE" />
      </concept>
      <concept>
        <code value="OMIM:613254" />
        <display value="TUBEROUS SCLEROSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:613255" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15" />
      </concept>
      <concept>
        <code value="OMIM:613265" />
        <display value="WAARDENBURG SYNDROME, TYPE 4B" />
      </concept>
      <concept>
        <code value="OMIM:613266" />
        <display value="WAARDENBURG SYNDROME, TYPE 4C" />
      </concept>
      <concept>
        <code value="OMIM:613267" />
        <display value="CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:613268" />
        <display value="CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:613269" />
        <display value="CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:613270" />
        <display value="CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:613271" />
        <display value="CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 7" />
      </concept>
      <concept>
        <code value="OMIM:613280" />
        <display value="HYPERMANGANESEMIA WITH DYSTONIA 1" />
      </concept>
      <concept>
        <code value="OMIM:613282" />
        <display value="FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:613284" />
        <display value="HEMATOCRIT/HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 3" />
      </concept>
      <concept>
        <code value="OMIM:613285" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 25" />
      </concept>
      <concept>
        <code value="OMIM:613286" />
        <display value="CARDIOMYOPATHY, DILATED, 1FF" />
      </concept>
      <concept>
        <code value="OMIM:613287" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N" />
      </concept>
      <concept>
        <code value="OMIM:613290" />
        <display value="HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:613291" />
        <display value="BILE ACID MALABSORPTION, PRIMARY" />
      </concept>
      <concept>
        <code value="OMIM:613307" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 79" />
      </concept>
      <concept>
        <code value="OMIM:613308" />
        <display value="DIAMOND-BLACKFAN ANEMIA 9" />
      </concept>
      <concept>
        <code value="OMIM:613309" />
        <display value="DIAMOND-BLACKFAN ANEMIA 10" />
      </concept>
      <concept>
        <code value="OMIM:613310" />
        <display value="EXUDATIVE VITREORETINOPATHY 5" />
      </concept>
      <concept>
        <code value="OMIM:613312" />
        <display value="HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:613313" />
        <display value="HEMOCHROMATOSIS, TYPE 2B" />
      </concept>
      <concept>
        <code value="OMIM:613318" />
        <display value="MIYOSHI MUSCULAR DYSTROPHY 2" />
      </concept>
      <concept>
        <code value="OMIM:613319" />
        <display value="MIYOSHI MUSCULAR DYSTROPHY 3" />
      </concept>
      <concept>
        <code value="OMIM:613320" />
        <display value="SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:613325" />
        <display value="RHABDOID TUMOR PREDISPOSITION SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:613327" />
        <display value="LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:613328" />
        <display value="ROIFMAN-CHITAYAT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613329" />
        <display value="PLASMINOGEN ACTIVATOR INHIBITOR-1 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613330" />
        <display value="SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:613339" />
        <display value="EPILEPSY, HOT WATER, 1" />
      </concept>
      <concept>
        <code value="OMIM:613340" />
        <display value="EPILEPSY, HOT WATER, 2" />
      </concept>
      <concept>
        <code value="OMIM:613341" />
        <display value="LEBER CONGENITAL AMAUROSIS 14" />
      </concept>
      <concept>
        <code value="OMIM:613342" />
        <display value="MSELENI JOINT DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:613343" />
        <display value="HANDIGODU JOINT DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:613345" />
        <display value="HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:613347" />
        <display value="PANCREATIC CANCER, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613348" />
        <display value="PANCREATIC CANCER, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:613353" />
        <display value="MONONEUROPATHY OF THE MEDIAN NERVE, MILD" />
      </concept>
      <concept>
        <code value="OMIM:613355" />
        <display value="CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613364" />
        <display value="SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:613370" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10" />
      </concept>
      <concept>
        <code value="OMIM:613371" />
        <display value="SPINOCEREBELLAR ATAXIA 30" />
      </concept>
      <concept>
        <code value="OMIM:613375" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11" />
      </concept>
      <concept>
        <code value="OMIM:613376" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC" />
      </concept>
      <concept>
        <code value="OMIM:613382" />
        <display value="BRACHYDACTYLY, TYPE E2" />
      </concept>
      <concept>
        <code value="OMIM:613385" />
        <display value="AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:613387" />
        <display value="FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613388" />
        <display value="FANCONI RENOTUBULAR SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:613390" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP O" />
      </concept>
      <concept>
        <code value="OMIM:613391" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 84A" />
      </concept>
      <concept>
        <code value="OMIM:613392" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 85" />
      </concept>
      <concept>
        <code value="OMIM:613393" />
        <display value="BIRBECK GRANULE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613398" />
        <display value="WARSAW BREAKAGE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613399" />
        <display value="BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:613402" />
        <display value="MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:613404" />
        <display value="ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2" />
      </concept>
      <concept>
        <code value="OMIM:613406" />
        <display value="WITTEVEEN-KOLK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613407" />
        <display value="LEPROSY, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:613410" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 16" />
      </concept>
      <concept>
        <code value="OMIM:613411" />
        <display value="OGUCHI DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:613412" />
        <display value="ESOPHAGITIS, EOSINOPHILIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:613418" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15" />
      </concept>
      <concept>
        <code value="OMIM:613424" />
        <display value="CARDIOMYOPATHY, DILATED, 1R" />
      </concept>
      <concept>
        <code value="OMIM:613426" />
        <display value="CARDIOMYOPATHY, DILATED, 1S" />
      </concept>
      <concept>
        <code value="OMIM:613428" />
        <display value="RETINITIS PIGMENTOSA 54" />
      </concept>
      <concept>
        <code value="OMIM:613435" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 12" />
      </concept>
      <concept>
        <code value="OMIM:613436" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 17" />
      </concept>
      <concept>
        <code value="OMIM:613440" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 21" />
      </concept>
      <concept>
        <code value="OMIM:613443" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 20" />
      </concept>
      <concept>
        <code value="OMIM:613444" />
        <display value="CHROMOSOME 16p11.2 DELETION SYNDROME, 220-KB" />
      </concept>
      <concept>
        <code value="OMIM:613451" />
        <display value="FRONTONASAL DYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:613453" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 91" />
      </concept>
      <concept>
        <code value="OMIM:613454" />
        <display value="RETT SYNDROME, CONGENITAL VARIANT" />
      </concept>
      <concept>
        <code value="OMIM:613456" />
        <display value="FRONTONASAL DYSPLASIA 3" />
      </concept>
      <concept>
        <code value="OMIM:613457" />
        <display value="CHROMOSOME 14q11-q22 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613458" />
        <display value="CHROMOSOME 16p13.3 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613459" />
        <display value="BIRTH WEIGHT QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:613460" />
        <display value="FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 6" />
      </concept>
      <concept>
        <code value="OMIM:613462" />
        <display value="FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:613463" />
        <display value="FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:613464" />
        <display value="RETINITIS PIGMENTOSA 51" />
      </concept>
      <concept>
        <code value="OMIM:613470" />
        <display value="HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613471" />
        <display value="REYNOLDS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613477" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5" />
      </concept>
      <concept>
        <code value="OMIM:613480" />
        <display value="LYMPHEDEMA, HEREDITARY, IC" />
      </concept>
      <concept>
        <code value="OMIM:613485" />
        <display value="LONG QT SYNDROME 13" />
      </concept>
      <concept>
        <code value="OMIM:613488" />
        <display value="MYXOID LIPOSARCOMA" />
      </concept>
      <concept>
        <code value="OMIM:613489" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj" />
      </concept>
      <concept>
        <code value="OMIM:613490" />
        <display value="ALPHA-1-ANTITRYPSIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613493" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 3" />
      </concept>
      <concept>
        <code value="OMIM:613494" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 4" />
      </concept>
      <concept>
        <code value="OMIM:613495" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 5" />
      </concept>
      <concept>
        <code value="OMIM:613496" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 6" />
      </concept>
      <concept>
        <code value="OMIM:613498" />
        <display value="SEX HORMONE-BINDING GLOBULIN CIRCULATING LEVEL QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:613500" />
        <display value="AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613501" />
        <display value="AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613502" />
        <display value="AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613506" />
        <display value="AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:613507" />
        <display value="GLYCOGEN STORAGE DISEASE XV" />
      </concept>
      <concept>
        <code value="OMIM:613508" />
        <display value="SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:613509" />
        <display value="CHROMOSOME 4q21 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613517" />
        <display value="MICROPHTHALMIA, ISOLATED 6" />
      </concept>
      <concept>
        <code value="OMIM:613518" />
        <display value="DERMATITIS, ATOPIC, 8" />
      </concept>
      <concept>
        <code value="OMIM:613519" />
        <display value="DERMATITIS, ATOPIC, 9" />
      </concept>
      <concept>
        <code value="OMIM:613523" />
        <display value="CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613530" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H" />
      </concept>
      <concept>
        <code value="OMIM:613533" />
        <display value="CHROMOSOME 17q21.31 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613544" />
        <display value="CHROMOSOME 6q11-q14 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613545" />
        <display value="MACROSTOMIA, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:613546" />
        <display value="AROMATASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613547" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 22" />
      </concept>
      <concept>
        <code value="OMIM:613548" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 23" />
      </concept>
      <concept>
        <code value="OMIM:613549" />
        <display value="STATURE QUANTITATIVE TRAIT LOCUS 24" />
      </concept>
      <concept>
        <code value="OMIM:613550" />
        <display value="NEPHRONOPHTHISIS 11" />
      </concept>
      <concept>
        <code value="OMIM:613551" />
        <display value="AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:613554" />
        <display value="VON WILLEBRAND DISEASE, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:613558" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 51" />
      </concept>
      <concept>
        <code value="OMIM:613559" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7" />
      </concept>
      <concept>
        <code value="OMIM:613561" />
        <display value="MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2" />
      </concept>
      <concept>
        <code value="OMIM:613563" />
        <display value="NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA" />
      </concept>
      <concept>
        <code value="OMIM:613564" />
        <display value="CHROMOSOME 2p12-p11.2 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613566" />
        <display value="FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6" />
      </concept>
      <concept>
        <code value="OMIM:613571" />
        <display value="DISORDERED STEROIDOGENESIS DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613573" />
        <display value="ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:613575" />
        <display value="RETINITIS PIGMENTOSA 55" />
      </concept>
      <concept>
        <code value="OMIM:613576" />
        <display value="ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:613581" />
        <display value="RETINITIS PIGMENTOSA 56" />
      </concept>
      <concept>
        <code value="OMIM:613582" />
        <display value="RETINITIS PIGMENTOSA 57" />
      </concept>
      <concept>
        <code value="OMIM:613587" />
        <display value="OCCULT MACULAR DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:613589" />
        <display value="LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6" />
      </concept>
      <concept>
        <code value="OMIM:613600" />
        <display value="TORSADE DE POINTES, SHORT-COUPLED VARIANT" />
      </concept>
      <concept>
        <code value="OMIM:613601" />
        <display value="EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION" />
      </concept>
      <concept>
        <code value="OMIM:613603" />
        <display value="CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613604" />
        <display value="CHROMOSOME 16p12.2-p11.2 DELETION SYNDROME, 7.1- TO 8.7-MB" />
      </concept>
      <concept>
        <code value="OMIM:613606" />
        <display value="FORSYTHE-WAKELING SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613608" />
        <display value="EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:613610" />
        <display value="CRANIOECTODERMAL DYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:613611" />
        <display value="CHOANAL ATRESIA AND LYMPHEDEMA" />
      </concept>
      <concept>
        <code value="OMIM:613612" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi" />
      </concept>
      <concept>
        <code value="OMIM:613615" />
        <display value="SENIOR-LOKEN SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:613616" />
        <display value="HYPEROXALURIA, PRIMARY, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:613617" />
        <display value="RETINITIS PIGMENTOSA 58" />
      </concept>
      <concept>
        <code value="OMIM:613618" />
        <display value="CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613623" />
        <display value="AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA" />
      </concept>
      <concept>
        <code value="OMIM:613625" />
        <display value="FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2" />
      </concept>
      <concept>
        <code value="OMIM:613627" />
        <display value="BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY, PTOSIS, HEARING LOSS, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:613628" />
        <display value="ODONTOID HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:613630" />
        <display value="COCOON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613636" />
        <display value="TUBERCULIN SKIN TEST REACTIVITY, ABSENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:613637" />
        <display value="TUBERCULIN SKIN TEST REACTIVITY QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:613638" />
        <display value="CHROMOSOME 19p13.13 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613640" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC" />
      </concept>
      <concept>
        <code value="OMIM:613641" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B" />
      </concept>
      <concept>
        <code value="OMIM:613642" />
        <display value="CARDIOMYOPATHY, DILATED, 1GG" />
      </concept>
      <concept>
        <code value="OMIM:613643" />
        <display value="PARKINSON DISEASE 5, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:613646" />
        <display value="METHYLMALONIC ACIDURIA, TRANSIENT, DUE TO TRANSCOBALAMIN RECEPTOR DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:613647" />
        <display value="SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613652" />
        <display value="C1q DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613656" />
        <display value="MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13" />
      </concept>
      <concept>
        <code value="OMIM:613657" />
        <display value="D-2-HYDROXYGLUTARIC ACIDURIA 2" />
      </concept>
      <concept>
        <code value="OMIM:613658" />
        <display value="RAJAB SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613659" />
        <display value="GASTRIC CANCER" />
      </concept>
      <concept>
        <code value="OMIM:613660" />
        <display value="CONE-ROD DYSTROPHY 15" />
      </concept>
      <concept>
        <code value="OMIM:613661" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip" />
      </concept>
      <concept>
        <code value="OMIM:613662" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:613668" />
        <display value="MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:613670" />
        <display value="MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:613671" />
        <display value="MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS" />
      </concept>
      <concept>
        <code value="OMIM:613672" />
        <display value="SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613673" />
        <display value="ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:613674" />
        <display value="VESICOURETERAL REFLUX 3" />
      </concept>
      <concept>
        <code value="OMIM:613675" />
        <display value="CHROMOSOME 17q11.2 DELETION SYNDROME, 1.4-MB" />
      </concept>
      <concept>
        <code value="OMIM:613676" />
        <display value="SECKEL SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:613677" />
        <display value="HYPERALDOSTERONISM, FAMILIAL, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:613678" />
        <display value="BRACHYOLMIA TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:613679" />
        <display value="PROTHROMBIN DEFICIENCY, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:613680" />
        <display value="BEAULIEU-BOYCOTT-INNES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613681" />
        <display value="CHROMOSOME 2q31.1 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613684" />
        <display value="RUBINSTEIN-TAYBI SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:613685" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 83" />
      </concept>
      <concept>
        <code value="OMIM:613686" />
        <display value="SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613688" />
        <display value="LONG QT SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:613689" />
        <display value="MAMMARY-DIGITAL-NAIL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613690" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7" />
      </concept>
      <concept>
        <code value="OMIM:613693" />
        <display value="LONG QT SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:613694" />
        <display value="CARDIOMYOPATHY, DILATED, 1U" />
      </concept>
      <concept>
        <code value="OMIM:613695" />
        <display value="LONG QT SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:613697" />
        <display value="CARDIOMYOPATHY, DILATED, 1V" />
      </concept>
      <concept>
        <code value="OMIM:613700" />
        <display value="SUPERNUMERARY DER(22)t(8" />
      </concept>
      <concept>
        <code value="OMIM:613702" />
        <display value="KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:613703" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6" />
      </concept>
      <concept>
        <code value="OMIM:613704" />
        <display value="MICROPHTHALMIA, ISOLATED 7" />
      </concept>
      <concept>
        <code value="OMIM:613705" />
        <display value="OROFACIAL CLEFT 10" />
      </concept>
      <concept>
        <code value="OMIM:613706" />
        <display value="NOONAN SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:613707" />
        <display value="LEOPARD SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:613708" />
        <display value="NEUROPATHY, HEREDITARY SENSORY, TYPE ID" />
      </concept>
      <concept>
        <code value="OMIM:613710" />
        <display value="THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:613711" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:613712" />
        <display value="HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:613717" />
        <display value="TREACHER COLLINS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:613718" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 74" />
      </concept>
      <concept>
        <code value="OMIM:613720" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7" />
      </concept>
      <concept>
        <code value="OMIM:613721" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11" />
      </concept>
      <concept>
        <code value="OMIM:613722" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12" />
      </concept>
      <concept>
        <code value="OMIM:613723" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 17" />
      </concept>
      <concept>
        <code value="OMIM:613724" />
        <display value="LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY" />
      </concept>
      <concept>
        <code value="OMIM:613728" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10" />
      </concept>
      <concept>
        <code value="OMIM:613729" />
        <display value="CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB" />
      </concept>
      <concept>
        <code value="OMIM:613730" />
        <display value="HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS" />
      </concept>
      <concept>
        <code value="OMIM:613731" />
        <display value="RETINITIS PIGMENTOSA 4" />
      </concept>
      <concept>
        <code value="OMIM:613735" />
        <display value="BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:613736" />
        <display value="ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:613737" />
        <display value="ACNE INVERSA, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:613743" />
        <display value="ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE" />
      </concept>
      <concept>
        <code value="OMIM:613744" />
        <display value="SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613750" />
        <display value="RETINITIS PIGMENTOSA 27" />
      </concept>
      <concept>
        <code value="OMIM:613751" />
        <display value="HETEROTAXY, VISCERAL, 4, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:613752" />
        <display value="HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613756" />
        <display value="RETINITIS PIGMENTOSA 49" />
      </concept>
      <concept>
        <code value="OMIM:613757" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 6" />
      </concept>
      <concept>
        <code value="OMIM:613758" />
        <display value="RETINITIS PIGMENTOSA 47" />
      </concept>
      <concept>
        <code value="OMIM:613759" />
        <display value="INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:613761" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 5" />
      </concept>
      <concept>
        <code value="OMIM:613762" />
        <display value="46,XY SEX REVERSAL 6" />
      </concept>
      <concept>
        <code value="OMIM:613763" />
        <display value="CATARACT 16, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:613765" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9" />
      </concept>
      <concept>
        <code value="OMIM:613767" />
        <display value="RETINITIS PIGMENTOSA 45" />
      </concept>
      <concept>
        <code value="OMIM:613769" />
        <display value="RETINITIS PIGMENTOSA 44" />
      </concept>
      <concept>
        <code value="OMIM:613776" />
        <display value="CHROMOSOME 17p13.1 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613778" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 8" />
      </concept>
      <concept>
        <code value="OMIM:613779" />
        <display value="COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:613780" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 7" />
      </concept>
      <concept>
        <code value="OMIM:613783" />
        <display value="COMPLEMENT COMPONENT C1s DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613784" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 12" />
      </concept>
      <concept>
        <code value="OMIM:613789" />
        <display value="COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II" />
      </concept>
      <concept>
        <code value="OMIM:613790" />
        <display value="COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I" />
      </concept>
      <concept>
        <code value="OMIM:613791" />
        <display value="MASP2 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613792" />
        <display value="CHROMOSOME 3pter-p25 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613793" />
        <display value="BLOOD GROUP, CROMER SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:613794" />
        <display value="RETINITIS PIGMENTOSA 20" />
      </concept>
      <concept>
        <code value="OMIM:613795" />
        <display value="LOEYS-DIETZ SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:613796" />
        <display value="IMMUNODEFICIENCY 31B" />
      </concept>
      <concept>
        <code value="OMIM:613800" />
        <display value="MEIER-GORLIN SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:613801" />
        <display value="RETINITIS PIGMENTOSA 40" />
      </concept>
      <concept>
        <code value="OMIM:613803" />
        <display value="MEIER-GORLIN SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:613804" />
        <display value="MEIER-GORLIN SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:613805" />
        <display value="MEIER-GORLIN SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:613806" />
        <display value="CHOLANGITIS, PRIMARY SCLEROSING" />
      </concept>
      <concept>
        <code value="OMIM:613807" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 14" />
      </concept>
      <concept>
        <code value="OMIM:613808" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 15" />
      </concept>
      <concept>
        <code value="OMIM:613809" />
        <display value="RETINITIS PIGMENTOSA 39" />
      </concept>
      <concept>
        <code value="OMIM:613810" />
        <display value="RETINITIS PIGMENTOSA 43" />
      </concept>
      <concept>
        <code value="OMIM:613811" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 2D" />
      </concept>
      <concept>
        <code value="OMIM:613812" />
        <display value="BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:613818" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9" />
      </concept>
      <concept>
        <code value="OMIM:613819" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:613820" />
        <display value="NEPHRONOPHTHISIS 12" />
      </concept>
      <concept>
        <code value="OMIM:613823" />
        <display value="SECKEL SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:613824" />
        <display value="NEPHRONOPHTHISIS 9" />
      </concept>
      <concept>
        <code value="OMIM:613825" />
        <display value="COMPLEMENT COMPONENT 9 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613826" />
        <display value="LEBER CONGENITAL AMAUROSIS 6" />
      </concept>
      <concept>
        <code value="OMIM:613827" />
        <display value="RETINITIS PIGMENTOSA 48" />
      </concept>
      <concept>
        <code value="OMIM:613828" />
        <display value="GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8" />
      </concept>
      <concept>
        <code value="OMIM:613829" />
        <display value="LEBER CONGENITAL AMAUROSIS 7" />
      </concept>
      <concept>
        <code value="OMIM:613830" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D" />
      </concept>
      <concept>
        <code value="OMIM:613834" />
        <display value="MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613835" />
        <display value="LEBER CONGENITAL AMAUROSIS 8" />
      </concept>
      <concept>
        <code value="OMIM:613836" />
        <display value="ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:613837" />
        <display value="LEBER CONGENITAL AMAUROSIS 11" />
      </concept>
      <concept>
        <code value="OMIM:613838" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16" />
      </concept>
      <concept>
        <code value="OMIM:613839" />
        <display value="MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613843" />
        <display value="LEBER CONGENITAL AMAUROSIS 15" />
      </concept>
      <concept>
        <code value="OMIM:613845" />
        <display value="HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613848" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE X" />
      </concept>
      <concept>
        <code value="OMIM:613849" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XII" />
      </concept>
      <concept>
        <code value="OMIM:613850" />
        <display value="INOSINE TRIPHOSPHATASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613852" />
        <display value="FUCOSYLTRANSFERASE 6 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613854" />
        <display value="CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6" />
      </concept>
      <concept>
        <code value="OMIM:613855" />
        <display value="EPISODIC ATAXIA, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:613856" />
        <display value="ACHROMATOPSIA 4" />
      </concept>
      <concept>
        <code value="OMIM:613857" />
        <display value="OROFACIAL CLEFT 13" />
      </concept>
      <concept>
        <code value="OMIM:613860" />
        <display value="FICOLIN 3 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613861" />
        <display value="RETINITIS PIGMENTOSA 59" />
      </concept>
      <concept>
        <code value="OMIM:613862" />
        <display value="RETINITIS PIGMENTOSA 38" />
      </concept>
      <concept>
        <code value="OMIM:613863" />
        <display value="GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:613865" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 61" />
      </concept>
      <concept>
        <code value="OMIM:613869" />
        <display value="MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:613870" />
        <display value="HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:613873" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17" />
      </concept>
      <concept>
        <code value="OMIM:613874" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18" />
      </concept>
      <concept>
        <code value="OMIM:613876" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20" />
      </concept>
      <concept>
        <code value="OMIM:613877" />
        <display value="LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:613881" />
        <display value="CARDIOMYOPATHY, DILATED, 1HH" />
      </concept>
      <concept>
        <code value="OMIM:613882" />
        <display value="HYPOMAGNESEMIA 6, RENAL" />
      </concept>
      <concept>
        <code value="OMIM:613884" />
        <display value="CHROMOSOME 13q14 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:613885" />
        <display value="MECKEL SYNDROME, TYPE 8" />
      </concept>
      <concept>
        <code value="OMIM:613886" />
        <display value="OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:613887" />
        <display value="CATARACT 36" />
      </concept>
      <concept>
        <code value="OMIM:613908" />
        <display value="SPINOCEREBELLAR ATAXIA 35" />
      </concept>
      <concept>
        <code value="OMIM:613909" />
        <display value="SPINOCEREBELLAR ATAXIA 32" />
      </concept>
      <concept>
        <code value="OMIM:613912" />
        <display value="COMPLEMENT FACTOR D DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613913" />
        <display value="LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS" />
      </concept>
      <concept>
        <code value="OMIM:613916" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 89" />
      </concept>
      <concept>
        <code value="OMIM:613925" />
        <display value="MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A" />
      </concept>
      <concept>
        <code value="OMIM:613926" />
        <display value="MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:613930" />
        <display value="ALOPECIA-MENTAL RETARDATION SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:613933" />
        <display value="ACETYL-CoA CARBOXYLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613938" />
        <display value="PARASOMNIA, SLEEPWALKING TYPE" />
      </concept>
      <concept>
        <code value="OMIM:613943" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8" />
      </concept>
      <concept>
        <code value="OMIM:613944" />
        <display value="IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:613949" />
        <display value="OKT4 EPITOPE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:613950" />
        <display value="SCHIZOPHRENIA 15" />
      </concept>
      <concept>
        <code value="OMIM:613951" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP P" />
      </concept>
      <concept>
        <code value="OMIM:613953" />
        <display value="IMMUNODEFICIENCY 51" />
      </concept>
      <concept>
        <code value="OMIM:613954" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:613955" />
        <display value="AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2" />
      </concept>
      <concept>
        <code value="OMIM:613956" />
        <display value="CANDIDIASIS, FAMILIAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:613957" />
        <display value="SPERMATOGENIC FAILURE 8" />
      </concept>
      <concept>
        <code value="OMIM:613958" />
        <display value="SPERMATOGENIC FAILURE 9" />
      </concept>
      <concept>
        <code value="OMIM:613959" />
        <display value="SCHIZOPHRENIA 16" />
      </concept>
      <concept>
        <code value="OMIM:613960" />
        <display value="GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:613969" />
        <display value="MYOPIA 19, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:613970" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:613972" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:613977" />
        <display value="CYANOSIS, TRANSIENT NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:613978" />
        <display value="HEMOGLOBIN H DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:613980" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 9" />
      </concept>
      <concept>
        <code value="OMIM:613981" />
        <display value="HYPOTRICHOSIS 3" />
      </concept>
      <concept>
        <code value="OMIM:613982" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE VI" />
      </concept>
      <concept>
        <code value="OMIM:613983" />
        <display value="RETINITIS PIGMENTOSA 60" />
      </concept>
      <concept>
        <code value="OMIM:613985" />
        <display value="BETA-THALASSEMIA" />
      </concept>
      <concept>
        <code value="OMIM:613986" />
        <display value="PITUITARY HORMONE DEFICIENCY, COMBINED, 6" />
      </concept>
      <concept>
        <code value="OMIM:613987" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:613988" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:613989" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:613990" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3" />
      </concept>
      <concept>
        <code value="OMIM:614008" />
        <display value="NESTOR-GUILLERMO PROGERIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614009" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614017" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 16" />
      </concept>
      <concept>
        <code value="OMIM:614018" />
        <display value="EPILEPSY, PROGRESSIVE MYOCLONIC, 6" />
      </concept>
      <concept>
        <code value="OMIM:614019" />
        <display value="LISSENCEPHALY 4" />
      </concept>
      <concept>
        <code value="OMIM:614020" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14" />
      </concept>
      <concept>
        <code value="OMIM:614021" />
        <display value="VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:614022" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 10" />
      </concept>
      <concept>
        <code value="OMIM:614023" />
        <display value="PHOSPHOSERINE PHOSPHATASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614024" />
        <display value="PROTEIN Z DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614025" />
        <display value="HEPATIC LIPASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614028" />
        <display value="APOLIPOPROTEIN C-III DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614033" />
        <display value="HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614034" />
        <display value="HEME OXYGENASE 1 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614035" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 29" />
      </concept>
      <concept>
        <code value="OMIM:614036" />
        <display value="ALPHA-2-MACROGLOBULIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614037" />
        <display value="LEUKOTRIENE C4 SYNTHASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614038" />
        <display value="LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:614039" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1" />
      </concept>
      <concept>
        <code value="OMIM:614042" />
        <display value="MOYAMOYA DISEASE 5" />
      </concept>
      <concept>
        <code value="OMIM:614044" />
        <display value="TRYPSINOGEN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614049" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 11" />
      </concept>
      <concept>
        <code value="OMIM:614050" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 12" />
      </concept>
      <concept>
        <code value="OMIM:614052" />
        <display value="MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:614053" />
        <display value="MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:614055" />
        <display value="ACETYL-CoA ACETYLTRANSFERASE-2 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614063" />
        <display value="N-ACETYLASPARTATE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614065" />
        <display value="MYOPATHY, DISTAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:614066" />
        <display value="SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614067" />
        <display value="SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614069" />
        <display value="IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614070" />
        <display value="PSORIASIS 13, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614072" />
        <display value="HERMANSKY-PUDLAK SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614073" />
        <display value="HERMANSKY-PUDLAK SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:614074" />
        <display value="HERMANSKY-PUDLAK SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:614075" />
        <display value="HERMANSKY-PUDLAK SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:614076" />
        <display value="HERMANSKY-PUDLAK SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:614077" />
        <display value="HERMANSKY-PUDLAK SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:614078" />
        <display value="CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614079" />
        <display value="ASPERGILLOSIS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614080" />
        <display value="MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:614081" />
        <display value="ANHAPTOGLOBINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:614082" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP G" />
      </concept>
      <concept>
        <code value="OMIM:614083" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP L" />
      </concept>
      <concept>
        <code value="OMIM:614089" />
        <display value="ATRIAL SEPTAL DEFECT 3" />
      </concept>
      <concept>
        <code value="OMIM:614090" />
        <display value="SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614091" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:614096" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8" />
      </concept>
      <concept>
        <code value="OMIM:614097" />
        <display value="ACATALASEMIA" />
      </concept>
      <concept>
        <code value="OMIM:614098" />
        <display value="KEPPEN-LUBINSKY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614099" />
        <display value="CRANIOECTODERMAL DYSPLASIA 3" />
      </concept>
      <concept>
        <code value="OMIM:614100" />
        <display value="CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE" />
      </concept>
      <concept>
        <code value="OMIM:614101" />
        <display value="PLASMA FIBRONECTIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614102" />
        <display value="IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614103" />
        <display value="LIPEDEMA" />
      </concept>
      <concept>
        <code value="OMIM:614104" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 7" />
      </concept>
      <concept>
        <code value="OMIM:614105" />
        <display value="METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614111" />
        <display value="PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614113" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:614114" />
        <display value="MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614115" />
        <display value="CORTICAL MALFORMATIONS, OCCIPITAL" />
      </concept>
      <concept>
        <code value="OMIM:614116" />
        <display value="NEUROPATHY, HEREDITARY SENSORY, TYPE IE" />
      </concept>
      <concept>
        <code value="OMIM:614120" />
        <display value="HYDROLETHALUS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614122" />
        <display value="CHITOTRIOSIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614128" />
        <display value="LACTATE DEHYDROGENASE B DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614129" />
        <display value="PERRAULT SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614131" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6" />
      </concept>
      <concept>
        <code value="OMIM:614134" />
        <display value="STICKLER SYNDROME, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:614135" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, 6" />
      </concept>
      <concept>
        <code value="OMIM:614149" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9" />
      </concept>
      <concept>
        <code value="OMIM:614152" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 64" />
      </concept>
      <concept>
        <code value="OMIM:614153" />
        <display value="SPINOCEREBELLAR ATAXIA 36" />
      </concept>
      <concept>
        <code value="OMIM:614156" />
        <display value="HYPERBILIVERDINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:614157" />
        <display value="NAIL DISORDER, NONSYNDROMIC CONGENITAL, 10" />
      </concept>
      <concept>
        <code value="OMIM:614158" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 14" />
      </concept>
      <concept>
        <code value="OMIM:614160" />
        <display value="MUSCLE HYPERTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:614162" />
        <display value="IMMUNODEFICIENCY 31C" />
      </concept>
      <concept>
        <code value="OMIM:614163" />
        <display value="DELAYED SLEEP PHASE DISORDER, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614164" />
        <display value="GLUTATHIONE PEROXIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614165" />
        <display value="PARAGANGLIOMAS 5" />
      </concept>
      <concept>
        <code value="OMIM:614166" />
        <display value="MYOPIA 20, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:614167" />
        <display value="MYOPIA 21, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:614170" />
        <display value="BRITTLE CORNEA SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614171" />
        <display value="HERMANSKY-PUDLAK SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:614172" />
        <display value="IMMUNODEFICIENCY 21" />
      </concept>
      <concept>
        <code value="OMIM:614173" />
        <display value="JOUBERT SYNDROME 13" />
      </concept>
      <concept>
        <code value="OMIM:614175" />
        <display value="MECKEL SYNDROME, TYPE 10" />
      </concept>
      <concept>
        <code value="OMIM:614180" />
        <display value="RETINITIS PIGMENTOSA 61" />
      </concept>
      <concept>
        <code value="OMIM:614181" />
        <display value="RETINITIS PIGMENTOSA 62" />
      </concept>
      <concept>
        <code value="OMIM:614185" />
        <display value="GELEOPHYSIC DYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:614186" />
        <display value="LEBER CONGENITAL AMAUROSIS 16" />
      </concept>
      <concept>
        <code value="OMIM:614187" />
        <display value="HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:614188" />
        <display value="CRANIOSYNOSTOSIS AND DENTAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:614190" />
        <display value="PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3" />
      </concept>
      <concept>
        <code value="OMIM:614192" />
        <display value="MACROCEPHALY, MACROSOMIA, AND FACIAL DYSMORPHISM SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614193" />
        <display value="TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2" />
      </concept>
      <concept>
        <code value="OMIM:614195" />
        <display value="CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614196" />
        <display value="NEPHROTIC SYNDROME, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:614198" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 16" />
      </concept>
      <concept>
        <code value="OMIM:614199" />
        <display value="NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:614200" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 9" />
      </concept>
      <concept>
        <code value="OMIM:614201" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 11" />
      </concept>
      <concept>
        <code value="OMIM:614202" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15" />
      </concept>
      <concept>
        <code value="OMIM:614203" />
        <display value="PARKINSON DISEASE 17" />
      </concept>
      <concept>
        <code value="OMIM:614204" />
        <display value="PSORIASIS 14, PUSTULAR" />
      </concept>
      <concept>
        <code value="OMIM:614205" />
        <display value="THREE M SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614207" />
        <display value="HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614208" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16" />
      </concept>
      <concept>
        <code value="OMIM:614209" />
        <display value="MECKEL SYNDROME, TYPE 9" />
      </concept>
      <concept>
        <code value="OMIM:614210" />
        <display value="LUNG CANCER SUSCEPTIBILITY 5" />
      </concept>
      <concept>
        <code value="OMIM:614211" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 33" />
      </concept>
      <concept>
        <code value="OMIM:614212" />
        <display value="ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:614213" />
        <display value="NEUROPATHY, HEREDITARY SENSORY, TYPE IIC" />
      </concept>
      <concept>
        <code value="OMIM:614219" />
        <display value="ADAMS-OLIVER SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614220" />
        <display value="BILIARY CIRRHOSIS, PRIMARY, 4" />
      </concept>
      <concept>
        <code value="OMIM:614221" />
        <display value="BILIARY CIRRHOSIS, PRIMARY, 5" />
      </concept>
      <concept>
        <code value="OMIM:614222" />
        <display value="WARBURG MICRO SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614223" />
        <display value="NARCOLEPSY 6, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614224" />
        <display value="RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS" />
      </concept>
      <concept>
        <code value="OMIM:614225" />
        <display value="WARBURG MICRO SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614226" />
        <display value="HOLOPROSENCEPHALY 11" />
      </concept>
      <concept>
        <code value="OMIM:614227" />
        <display value="HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3" />
      </concept>
      <concept>
        <code value="OMIM:614228" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O" />
      </concept>
      <concept>
        <code value="OMIM:614229" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11" />
      </concept>
      <concept>
        <code value="OMIM:614230" />
        <display value="CHROMOSOME 8q21.11 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614231" />
        <display value="MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614233" />
        <display value="HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1" />
      </concept>
      <concept>
        <code value="OMIM:614237" />
        <display value="HYPOTRICHOSIS 9" />
      </concept>
      <concept>
        <code value="OMIM:614238" />
        <display value="HYPOTRICHOSIS 10" />
      </concept>
      <concept>
        <code value="OMIM:614249" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 18" />
      </concept>
      <concept>
        <code value="OMIM:614250" />
        <display value="NARCOLEPSY 7" />
      </concept>
      <concept>
        <code value="OMIM:614251" />
        <display value="PARKINSON DISEASE 18, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614252" />
        <display value="ANEURYSM, INTRACRANIAL BERRY, 11" />
      </concept>
      <concept>
        <code value="OMIM:614254" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:614255" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 9" />
      </concept>
      <concept>
        <code value="OMIM:614256" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 10" />
      </concept>
      <concept>
        <code value="OMIM:614257" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 11" />
      </concept>
      <concept>
        <code value="OMIM:614261" />
        <display value="MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614262" />
        <display value="ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY" />
      </concept>
      <concept>
        <code value="OMIM:614265" />
        <display value="COMBINED MALONIC AND METHYLMALONIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:614266" />
        <display value="BARRETT ESOPHAGUS" />
      </concept>
      <concept>
        <code value="OMIM:614278" />
        <display value="PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614279" />
        <display value="46,XY SEX REVERSAL 8" />
      </concept>
      <concept>
        <code value="OMIM:614280" />
        <display value="EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:614284" />
        <display value="STICKLER SYNDROME, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:614286" />
        <display value="MYELODYSPLASTIC SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614290" />
        <display value="TETRASOMY 18p" />
      </concept>
      <concept>
        <code value="OMIM:614291" />
        <display value="BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:614292" />
        <display value="MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:614293" />
        <display value="HYDATIDIFORM MOLE, RECURRENT, 2" />
      </concept>
      <concept>
        <code value="OMIM:614294" />
        <display value="CHROMOSOME 15q25 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614296" />
        <display value="WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:614298" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4" />
      </concept>
      <concept>
        <code value="OMIM:614299" />
        <display value="MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:614300" />
        <display value="HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614302" />
        <display value="EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:614303" />
        <display value="EDICT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614305" />
        <display value="SCLEROSTEOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:614306" />
        <display value="COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:614307" />
        <display value="ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614317" />
        <display value="VESICOURETERAL REFLUX 4" />
      </concept>
      <concept>
        <code value="OMIM:614318" />
        <display value="VESICOURETERAL REFLUX 5" />
      </concept>
      <concept>
        <code value="OMIM:614319" />
        <display value="VESICOURETERAL REFLUX 6" />
      </concept>
      <concept>
        <code value="OMIM:614320" />
        <display value="PANCREATIC CANCER, SUSCEPTIBILITY TO, 4" />
      </concept>
      <concept>
        <code value="OMIM:614321" />
        <display value="MYOPATHY, DISTAL, TATEYAMA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614322" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12" />
      </concept>
      <concept>
        <code value="OMIM:614323" />
        <display value="NEVOID HYPERMELANOSIS, LINEAR AND WHORLED" />
      </concept>
      <concept>
        <code value="OMIM:614324" />
        <display value="OVARIAN DYSGENESIS 3" />
      </concept>
      <concept>
        <code value="OMIM:614325" />
        <display value="PITT-HOPKINS-LIKE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614326" />
        <display value="FEINGOLD SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614327" />
        <display value="TUMOR PREDISPOSITION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614328" />
        <display value="INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:614329" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 31" />
      </concept>
      <concept>
        <code value="OMIM:614331" />
        <display value="COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:614332" />
        <display value="CHROMOSOME 2p16.3 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614333" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 29" />
      </concept>
      <concept>
        <code value="OMIM:614335" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 1B" />
      </concept>
      <concept>
        <code value="OMIM:614337" />
        <display value="COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:614338" />
        <display value="PANCREATIC LIPASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614340" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27" />
      </concept>
      <concept>
        <code value="OMIM:614341" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 33" />
      </concept>
      <concept>
        <code value="OMIM:614342" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 30" />
      </concept>
      <concept>
        <code value="OMIM:614343" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 19" />
      </concept>
      <concept>
        <code value="OMIM:614344" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 23" />
      </concept>
      <concept>
        <code value="OMIM:614345" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 24" />
      </concept>
      <concept>
        <code value="OMIM:614346" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 25" />
      </concept>
      <concept>
        <code value="OMIM:614347" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 28" />
      </concept>
      <concept>
        <code value="OMIM:614350" />
        <display value="COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:614369" />
        <display value="PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS" />
      </concept>
      <concept>
        <code value="OMIM:614370" />
        <display value="SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5" />
      </concept>
      <concept>
        <code value="OMIM:614371" />
        <display value="DENGUE VIRUS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614372" />
        <display value="MANNOSE-BINDING LECTIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614373" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE" />
      </concept>
      <concept>
        <code value="OMIM:614374" />
        <display value="BLOOD GROUP, CHIDO/RODGERS SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:614375" />
        <display value="AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:614376" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:614377" />
        <display value="NEPHRONOPHTHISIS 13" />
      </concept>
      <concept>
        <code value="OMIM:614378" />
        <display value="CRANIOECTODERMAL DYSPLASIA 4" />
      </concept>
      <concept>
        <code value="OMIM:614379" />
        <display value="COMPLEMENT COMPONENT 4B DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614380" />
        <display value="COMPLEMENT COMPONENT 4A DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614381" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM" />
      </concept>
      <concept>
        <code value="OMIM:614382" />
        <display value="BACTEREMIA, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:614383" />
        <display value="BACTEREMIA, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:614385" />
        <display value="COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:614388" />
        <display value="ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1" />
      </concept>
      <concept>
        <code value="OMIM:614389" />
        <display value="PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1" />
      </concept>
      <concept>
        <code value="OMIM:614390" />
        <display value="PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2" />
      </concept>
      <concept>
        <code value="OMIM:614391" />
        <display value="PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:614395" />
        <display value="GRAFT-VERSUS-HOST DISEASE, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614399" />
        <display value="MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:614400" />
        <display value="GLUCOCORTICOID THERAPY, RESPONSE TO" />
      </concept>
      <concept>
        <code value="OMIM:614401" />
        <display value="ACCELERATED TUMOR FORMATION, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614402" />
        <display value="MICROPHTHALMIA, SYNDROMIC 11" />
      </concept>
      <concept>
        <code value="OMIM:614407" />
        <display value="MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614408" />
        <display value="MYOPATHY, CENTRONUCLEAR, 3" />
      </concept>
      <concept>
        <code value="OMIM:614409" />
        <display value="SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614411" />
        <display value="GLYCEROL QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:614414" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 96" />
      </concept>
      <concept>
        <code value="OMIM:614415" />
        <display value="CHILBLAIN LUPUS 2" />
      </concept>
      <concept>
        <code value="OMIM:614416" />
        <display value="RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:614417" />
        <display value="EPILEPSY, FAMILIAL TEMPORAL LOBE, 5" />
      </concept>
      <concept>
        <code value="OMIM:614418" />
        <display value="FEBRILE SEIZURES, FAMILIAL, 11" />
      </concept>
      <concept>
        <code value="OMIM:614419" />
        <display value="ASPARTATE AMINOTRANSFERASE, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1" />
      </concept>
      <concept>
        <code value="OMIM:614420" />
        <display value="SYSTEMIC LUPUS ERYTHEMATOSUS 16" />
      </concept>
      <concept>
        <code value="OMIM:614422" />
        <display value="CATARACT 37" />
      </concept>
      <concept>
        <code value="OMIM:614424" />
        <display value="JOUBERT SYNDROME 14" />
      </concept>
      <concept>
        <code value="OMIM:614429" />
        <display value="VENTRICULAR SEPTAL DEFECT 1" />
      </concept>
      <concept>
        <code value="OMIM:614430" />
        <display value="ATRIOVENTRICULAR SEPTAL DEFECT 4" />
      </concept>
      <concept>
        <code value="OMIM:614431" />
        <display value="VENTRICULAR SEPTAL DEFECT 2" />
      </concept>
      <concept>
        <code value="OMIM:614432" />
        <display value="VENTRICULAR SEPTAL DEFECT 3" />
      </concept>
      <concept>
        <code value="OMIM:614433" />
        <display value="ATRIAL SEPTAL DEFECT 8" />
      </concept>
      <concept>
        <code value="OMIM:614434" />
        <display value="CUTIS LAXA, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:614435" />
        <display value="HYPOPLASTIC LEFT HEART SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614436" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P" />
      </concept>
      <concept>
        <code value="OMIM:614437" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB" />
      </concept>
      <concept>
        <code value="OMIM:614438" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB" />
      </concept>
      <concept>
        <code value="OMIM:614441" />
        <display value="HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:614450" />
        <display value="HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6" />
      </concept>
      <concept>
        <code value="OMIM:614455" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E" />
      </concept>
      <concept>
        <code value="OMIM:614456" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:614457" />
        <display value="ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:614458" />
        <display value="THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:614462" />
        <display value="HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:614464" />
        <display value="JOUBERT SYNDROME 15" />
      </concept>
      <concept>
        <code value="OMIM:614465" />
        <display value="JOUBERT SYNDROME 16" />
      </concept>
      <concept>
        <code value="OMIM:614466" />
        <display value="CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:614468" />
        <display value="FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614470" />
        <display value="RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:614473" />
        <display value="ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2" />
      </concept>
      <concept>
        <code value="OMIM:614474" />
        <display value="ATRIOVENTRICULAR SEPTAL DEFECT 5" />
      </concept>
      <concept>
        <code value="OMIM:614475" />
        <display value="ATRIAL SEPTAL DEFECT 9" />
      </concept>
      <concept>
        <code value="OMIM:614480" />
        <display value="HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:614482" />
        <display value="CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:614483" />
        <display value="PORENCEPHALY 2" />
      </concept>
      <concept>
        <code value="OMIM:614485" />
        <display value="TRIGONOCEPHALY 2" />
      </concept>
      <concept>
        <code value="OMIM:614486" />
        <display value="THROMBOPHILIA DUE TO THROMBOMODULIN DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:614487" />
        <display value="SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614490" />
        <display value="BLOOD GROUP, JUNIOR SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:614491" />
        <display value="PSEUDOHYPOALDOSTERONISM, TYPE IIB" />
      </concept>
      <concept>
        <code value="OMIM:614492" />
        <display value="PSEUDOHYPOALDOSTERONISM, TYPE IIC" />
      </concept>
      <concept>
        <code value="OMIM:614493" />
        <display value="WISKOTT-ALDRICH SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614494" />
        <display value="RETINITIS PIGMENTOSA 63" />
      </concept>
      <concept>
        <code value="OMIM:614495" />
        <display value="PSEUDOHYPOALDOSTERONISM, TYPE IID" />
      </concept>
      <concept>
        <code value="OMIM:614496" />
        <display value="PSEUDOHYPOALDOSTERONISM, TYPE IIE" />
      </concept>
      <concept>
        <code value="OMIM:614497" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7" />
      </concept>
      <concept>
        <code value="OMIM:614498" />
        <display value="RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:614499" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:614500" />
        <display value="CONE-ROD DYSTROPHY 16" />
      </concept>
      <concept>
        <code value="OMIM:614501" />
        <display value="PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:614504" />
        <display value="USHER SYNDROME, TYPE IIIB" />
      </concept>
      <concept>
        <code value="OMIM:614507" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ir" />
      </concept>
      <concept>
        <code value="OMIM:614508" />
        <display value="MIRROR MOVEMENTS 2" />
      </concept>
      <concept>
        <code value="OMIM:614514" />
        <display value="THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614519" />
        <display value="HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614520" />
        <display value="ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614521" />
        <display value="THROMBOCYTHEMIA 3" />
      </concept>
      <concept>
        <code value="OMIM:614524" />
        <display value="FIBROCHONDROGENESIS 2" />
      </concept>
      <concept>
        <code value="OMIM:614526" />
        <display value="CHROMOSOME 17q12 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614527" />
        <display value="CHROMOSOME 17q12 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614541" />
        <display value="CHROMOSOME 16q22 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614546" />
        <display value="EFAVIRENZ, POOR METABOLISM OF" />
      </concept>
      <concept>
        <code value="OMIM:614557" />
        <display value="EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2" />
      </concept>
      <concept>
        <code value="OMIM:614558" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13" />
      </concept>
      <concept>
        <code value="OMIM:614559" />
        <display value="INFANTILE CEREBELLAR-RETINAL DEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:614561" />
        <display value="LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:614563" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 13" />
      </concept>
      <concept>
        <code value="OMIM:614564" />
        <display value="CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL" />
      </concept>
      <concept>
        <code value="OMIM:614565" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E" />
      </concept>
      <concept>
        <code value="OMIM:614569" />
        <display value="MULTIPLE ENCHONDROMATOSIS, MAFFUCCI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614575" />
        <display value="CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614576" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl" />
      </concept>
      <concept>
        <code value="OMIM:614582" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9" />
      </concept>
      <concept>
        <code value="OMIM:614583" />
        <display value="BARAITSER-WINTER SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614588" />
        <display value="DYSTONIA 21" />
      </concept>
      <concept>
        <code value="OMIM:614590" />
        <display value="PODOCONIOSIS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614592" />
        <display value="BENT BONE DYSPLASIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614594" />
        <display value="PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES" />
      </concept>
      <concept>
        <code value="OMIM:614595" />
        <display value="PREECLAMPSIA/ECLAMPSIA 5" />
      </concept>
      <concept>
        <code value="OMIM:614602" />
        <display value="TRICHOHEPATOENTERIC SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614607" />
        <display value="COFFIN-SIRIS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614608" />
        <display value="COFFIN-SIRIS SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614609" />
        <display value="COFFIN-SIRIS SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:614613" />
        <display value="ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:614614" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 4B" />
      </concept>
      <concept>
        <code value="OMIM:614615" />
        <display value="JOUBERT SYNDROME 17" />
      </concept>
      <concept>
        <code value="OMIM:614616" />
        <display value="DIARRHEA 6" />
      </concept>
      <concept>
        <code value="OMIM:614617" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 86" />
      </concept>
      <concept>
        <code value="OMIM:614618" />
        <display value="HYPEREKPLEXIA 3" />
      </concept>
      <concept>
        <code value="OMIM:614619" />
        <display value="HYPEREKPLEXIA 2" />
      </concept>
      <concept>
        <code value="OMIM:614621" />
        <display value="UV-SENSITIVE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614622" />
        <display value="KERATOCONUS 5" />
      </concept>
      <concept>
        <code value="OMIM:614623" />
        <display value="KERATOCONUS 6" />
      </concept>
      <concept>
        <code value="OMIM:614628" />
        <display value="KERATOCONUS 8" />
      </concept>
      <concept>
        <code value="OMIM:614629" />
        <display value="KERATOCONUS 7" />
      </concept>
      <concept>
        <code value="OMIM:614640" />
        <display value="UV-SENSITIVE SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614643" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7" />
      </concept>
      <concept>
        <code value="OMIM:614644" />
        <display value="MEAN PLATELET VOLUME QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:614645" />
        <display value="MEAN PLATELET VOLUME QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:614646" />
        <display value="MEAN PLATELET VOLUME QUANTITATIVE TRAIT LOCUS 6" />
      </concept>
      <concept>
        <code value="OMIM:614650" />
        <display value="COENZYME Q10 DEFICIENCY, PRIMARY, 6" />
      </concept>
      <concept>
        <code value="OMIM:614651" />
        <display value="COENZYME Q10 DEFICIENCY, PRIMARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:614652" />
        <display value="COENZYME Q10 DEFICIENCY, PRIMARY, 3" />
      </concept>
      <concept>
        <code value="OMIM:614653" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI" />
      </concept>
      <concept>
        <code value="OMIM:614654" />
        <display value="COENZYME Q10 DEFICIENCY, PRIMARY, 5" />
      </concept>
      <concept>
        <code value="OMIM:614655" />
        <display value="STUTTERING, FAMILIAL PERSISTENT, 3" />
      </concept>
      <concept>
        <code value="OMIM:614662" />
        <display value="CORTISONE REDUCTASE DEFICIENCY 2" />
      </concept>
      <concept>
        <code value="OMIM:614665" />
        <display value="MECONIUM ILEUS" />
      </concept>
      <concept>
        <code value="OMIM:614668" />
        <display value="STUTTERING, FAMILIAL PERSISTENT, 4" />
      </concept>
      <concept>
        <code value="OMIM:614669" />
        <display value="AURICULOCONDYLAR SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614670" />
        <display value="PERIPARTUM CARDIOMYOPATHY, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614671" />
        <display value="CHROMOSOME 16p11.2 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614672" />
        <display value="CARDIOMYOPATHY, DILATED, 2B" />
      </concept>
      <concept>
        <code value="OMIM:614673" />
        <display value="MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614674" />
        <display value="PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT" />
      </concept>
      <concept>
        <code value="OMIM:614675" />
        <display value="BONE MARROW FAILURE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:614676" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21" />
      </concept>
      <concept>
        <code value="OMIM:614678" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 1B" />
      </concept>
      <concept>
        <code value="OMIM:614679" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 17" />
      </concept>
      <concept>
        <code value="OMIM:614680" />
        <display value="INFLUENZA, SEVERE, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614684" />
        <display value="HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES" />
      </concept>
      <concept>
        <code value="OMIM:614687" />
        <display value="ALAR CLEFT, ISOLATED" />
      </concept>
      <concept>
        <code value="OMIM:614688" />
        <display value="PONTINE TEGMENTAL CAP DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:614689" />
        <display value="SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:614691" />
        <display value="CATARACT 38" />
      </concept>
      <concept>
        <code value="OMIM:614692" />
        <display value="MEMBRANOUS NEPHROPATHY, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614696" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 17" />
      </concept>
      <concept>
        <code value="OMIM:614699" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 7" />
      </concept>
      <concept>
        <code value="OMIM:614700" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY" />
      </concept>
      <concept>
        <code value="OMIM:614701" />
        <display value="CORNELIA DE LANGE SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:614702" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10" />
      </concept>
      <concept>
        <code value="OMIM:614706" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 11" />
      </concept>
      <concept>
        <code value="OMIM:614707" />
        <display value="BROWN-VIALETTO-VAN LAERE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614714" />
        <display value="POROKERATOSIS 7, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:614723" />
        <display value="ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614727" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIk" />
      </concept>
      <concept>
        <code value="OMIM:614728" />
        <display value="SECKEL SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:614731" />
        <display value="PROSTATE CANCER, HEREDITARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:614732" />
        <display value="INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, AND GENITAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:614736" />
        <display value="GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614739" />
        <display value="3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:614740" />
        <display value="BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:614741" />
        <display value="MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614742" />
        <display value="PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1" />
      </concept>
      <concept>
        <code value="OMIM:614743" />
        <display value="PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2" />
      </concept>
      <concept>
        <code value="OMIM:614744" />
        <display value="FACIAL PARESIS, HEREDITARY CONGENITAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:614745" />
        <display value="BLOOD GROUP, JOHN MILTON HAGEN SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:614746" />
        <display value="URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 5" />
      </concept>
      <concept>
        <code value="OMIM:614747" />
        <display value="URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 6" />
      </concept>
      <concept>
        <code value="OMIM:614748" />
        <display value="INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:614749" />
        <display value="HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614750" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 13" />
      </concept>
      <concept>
        <code value="OMIM:614751" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB" />
      </concept>
      <concept>
        <code value="OMIM:614752" />
        <display value="INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:614753" />
        <display value="SOTOS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614756" />
        <display value="CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:614779" />
        <display value="HETEROTAXY, VISCERAL, 6, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:614782" />
        <display value="TREMOR, HEREDITARY ESSENTIAL, 4" />
      </concept>
      <concept>
        <code value="OMIM:614800" />
        <display value="SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY" />
      </concept>
      <concept>
        <code value="OMIM:614807" />
        <display value="MYOPATHY, CENTRONUCLEAR, 4" />
      </concept>
      <concept>
        <code value="OMIM:614808" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 18" />
      </concept>
      <concept>
        <code value="OMIM:614809" />
        <display value="CFHR5 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614810" />
        <display value="MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:614813" />
        <display value="SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS" />
      </concept>
      <concept>
        <code value="OMIM:614814" />
        <display value="ADAMS-OLIVER SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614815" />
        <display value="JOUBERT SYNDROME 18" />
      </concept>
      <concept>
        <code value="OMIM:614816" />
        <display value="LOEYS-DIETZ SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:614817" />
        <display value="INTERSTITIAL NEPHRITIS, KARYOMEGALIC" />
      </concept>
      <concept>
        <code value="OMIM:614819" />
        <display value="WEILL-MARCHESANI SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:614820" />
        <display value="ALTERNATING HEMIPLEGIA OF CHILDHOOD 2" />
      </concept>
      <concept>
        <code value="OMIM:614822" />
        <display value="SPERMATOGENIC FAILURE 10" />
      </concept>
      <concept>
        <code value="OMIM:614823" />
        <display value="AORTIC VALVE DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:614826" />
        <display value="NYSTAGMUS 7, CONGENITAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:614830" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8" />
      </concept>
      <concept>
        <code value="OMIM:614831" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13" />
      </concept>
      <concept>
        <code value="OMIM:614832" />
        <display value="AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4" />
      </concept>
      <concept>
        <code value="OMIM:614833" />
        <display value="MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:614834" />
        <display value="THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:614836" />
        <display value="HUMAN HERPESVIRUS 8, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:614837" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614838" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614839" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614840" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614841" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614842" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614844" />
        <display value="NEPHRONOPHTHISIS 14" />
      </concept>
      <concept>
        <code value="OMIM:614845" />
        <display value="NEPHRONOPHTHISIS 15" />
      </concept>
      <concept>
        <code value="OMIM:614846" />
        <display value="TETRASOMY 15q26" />
      </concept>
      <concept>
        <code value="OMIM:614847" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12" />
      </concept>
      <concept>
        <code value="OMIM:614849" />
        <display value="ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 5" />
      </concept>
      <concept>
        <code value="OMIM:614850" />
        <display value="ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6" />
      </concept>
      <concept>
        <code value="OMIM:614851" />
        <display value="SECKEL SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:614852" />
        <display value="MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614856" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XIII" />
      </concept>
      <concept>
        <code value="OMIM:614857" />
        <display value="METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614858" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614859" />
        <display value="PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614860" />
        <display value="DYSTONIA 23" />
      </concept>
      <concept>
        <code value="OMIM:614861" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 98" />
      </concept>
      <concept>
        <code value="OMIM:614862" />
        <display value="PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614863" />
        <display value="PEROXISOME BIOGENESIS DISORDER 4B" />
      </concept>
      <concept>
        <code value="OMIM:614866" />
        <display value="PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614867" />
        <display value="PEROXISOME BIOGENESIS DISORDER 5B" />
      </concept>
      <concept>
        <code value="OMIM:614868" />
        <display value="T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:614869" />
        <display value="USHER SYNDROME, TYPE IJ" />
      </concept>
      <concept>
        <code value="OMIM:614870" />
        <display value="PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614871" />
        <display value="PEROXISOME BIOGENESIS DISORDER 6B" />
      </concept>
      <concept>
        <code value="OMIM:614872" />
        <display value="PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614873" />
        <display value="PEROXISOME BIOGENESIS DISORDER 7B" />
      </concept>
      <concept>
        <code value="OMIM:614874" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 18" />
      </concept>
      <concept>
        <code value="OMIM:614875" />
        <display value="METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:614876" />
        <display value="PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614877" />
        <display value="PEROXISOME BIOGENESIS DISORDER 8B" />
      </concept>
      <concept>
        <code value="OMIM:614878" />
        <display value="AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED" />
      </concept>
      <concept>
        <code value="OMIM:614879" />
        <display value="PEROXISOME BIOGENESIS DISORDER 9B" />
      </concept>
      <concept>
        <code value="OMIM:614880" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614881" />
        <display value="SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5" />
      </concept>
      <concept>
        <code value="OMIM:614882" />
        <display value="PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614883" />
        <display value="PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614885" />
        <display value="PEROXISOME BIOGENESIS DISORDER 11B" />
      </concept>
      <concept>
        <code value="OMIM:614886" />
        <display value="PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614887" />
        <display value="PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)" />
      </concept>
      <concept>
        <code value="OMIM:614889" />
        <display value="IMMUNODEFICIENCY 28" />
      </concept>
      <concept>
        <code value="OMIM:614890" />
        <display value="IMMUNODEFICIENCY 29" />
      </concept>
      <concept>
        <code value="OMIM:614891" />
        <display value="IMMUNODEFICIENCY 30" />
      </concept>
      <concept>
        <code value="OMIM:614892" />
        <display value="IMMUNODEFICIENCY 31A" />
      </concept>
      <concept>
        <code value="OMIM:614893" />
        <display value="IMMUNODEFICIENCY 32A" />
      </concept>
      <concept>
        <code value="OMIM:614895" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F" />
      </concept>
      <concept>
        <code value="OMIM:614896" />
        <display value="SINOATRIAL NODE DYSFUNCTION AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:614897" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:614898" />
        <display value="SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614899" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 93" />
      </concept>
      <concept>
        <code value="OMIM:614900" />
        <display value="DIAMOND-BLACKFAN ANEMIA 11" />
      </concept>
      <concept>
        <code value="OMIM:614915" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:614916" />
        <display value="VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4" />
      </concept>
      <concept>
        <code value="OMIM:614920" />
        <display value="PEROXISOME BIOGENESIS DISORDER 14B" />
      </concept>
      <concept>
        <code value="OMIM:614921" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It" />
      </concept>
      <concept>
        <code value="OMIM:614922" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11" />
      </concept>
      <concept>
        <code value="OMIM:614923" />
        <display value="BRANCHED-CHAIN KETO ACID DEHYDROGENASE KINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614924" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12" />
      </concept>
      <concept>
        <code value="OMIM:614926" />
        <display value="PERRAULT SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614927" />
        <display value="ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614928" />
        <display value="ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614929" />
        <display value="ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614931" />
        <display value="ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614932" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13" />
      </concept>
      <concept>
        <code value="OMIM:614934" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 70" />
      </concept>
      <concept>
        <code value="OMIM:614935" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 19" />
      </concept>
      <concept>
        <code value="OMIM:614936" />
        <display value="PALMOPLANTAR KERATODERMA, PUNCTATE TYPE IB" />
      </concept>
      <concept>
        <code value="OMIM:614937" />
        <display value="MYOCLONUS, FAMILIAL CORTICAL" />
      </concept>
      <concept>
        <code value="OMIM:614940" />
        <display value="ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:614941" />
        <display value="ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:614944" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 84B" />
      </concept>
      <concept>
        <code value="OMIM:614945" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 18B" />
      </concept>
      <concept>
        <code value="OMIM:614946" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14" />
      </concept>
      <concept>
        <code value="OMIM:614947" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15" />
      </concept>
      <concept>
        <code value="OMIM:614954" />
        <display value="CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3" />
      </concept>
      <concept>
        <code value="OMIM:614959" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14" />
      </concept>
      <concept>
        <code value="OMIM:614961" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 8" />
      </concept>
      <concept>
        <code value="OMIM:614962" />
        <display value="LEPTIN DEFICIENCY OR DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:614963" />
        <display value="LEPTIN RECEPTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:614969" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:614970" />
        <display value="JOUBERT SYNDROME 20" />
      </concept>
      <concept>
        <code value="OMIM:614972" />
        <display value="CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3" />
      </concept>
      <concept>
        <code value="OMIM:614973" />
        <display value="FOCAL FACIAL DERMAL DYSPLASIA 2, BRAUER-SETLEIS TYPE" />
      </concept>
      <concept>
        <code value="OMIM:614974" />
        <display value="FOCAL FACIAL DERMAL DYSPLASIA 4" />
      </concept>
      <concept>
        <code value="OMIM:614976" />
        <display value="CARPENTER SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:614979" />
        <display value="SPLENOMEGALY, CYTOPENIA, AND VISION LOSS" />
      </concept>
      <concept>
        <code value="OMIM:614980" />
        <display value="CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2" />
      </concept>
      <concept>
        <code value="OMIM:614990" />
        <display value="USHER SYNDROME, TYPE IK" />
      </concept>
      <concept>
        <code value="OMIM:615005" />
        <display value="EPILEPSY, NOCTURNAL FRONTAL LOBE, 5" />
      </concept>
      <concept>
        <code value="OMIM:615006" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15" />
      </concept>
      <concept>
        <code value="OMIM:615007" />
        <display value="BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4" />
      </concept>
      <concept>
        <code value="OMIM:615008" />
        <display value="NEPHROTIC SYNDROME, TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:615009" />
        <display value="SCHUURS-HOEIJMAKERS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615010" />
        <display value="AICARDI-GOUTIERES SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:615011" />
        <display value="PHOSPHOHYDROXYLYSINURIA" />
      </concept>
      <concept>
        <code value="OMIM:615021" />
        <display value="BLOOD GROUP, GLOBOSIDE SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:615022" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7" />
      </concept>
      <concept>
        <code value="OMIM:615023" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9" />
      </concept>
      <concept>
        <code value="OMIM:615024" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10" />
      </concept>
      <concept>
        <code value="OMIM:615025" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q" />
      </concept>
      <concept>
        <code value="OMIM:615026" />
        <display value="RIBOFLAVIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615028" />
        <display value="EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615030" />
        <display value="SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615031" />
        <display value="SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615032" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 18" />
      </concept>
      <concept>
        <code value="OMIM:615033" />
        <display value="SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615034" />
        <display value="DYSTONIA 24" />
      </concept>
      <concept>
        <code value="OMIM:615035" />
        <display value="SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615040" />
        <display value="EPISODIC PAIN SYNDROME, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:615041" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10" />
      </concept>
      <concept>
        <code value="OMIM:615042" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu" />
      </concept>
      <concept>
        <code value="OMIM:615043" />
        <display value="SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615048" />
        <display value="SPINAL MUSCULAR ATROPHY, JOKELA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:615058" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F" />
      </concept>
      <concept>
        <code value="OMIM:615059" />
        <display value="HYPOTRICHOSIS 11" />
      </concept>
      <concept>
        <code value="OMIM:615065" />
        <display value="ARTHROGRYPOSIS, DISTAL, TYPE 5D" />
      </concept>
      <concept>
        <code value="OMIM:615066" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XIV" />
      </concept>
      <concept>
        <code value="OMIM:615067" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 20" />
      </concept>
      <concept>
        <code value="OMIM:615071" />
        <display value="ALAZAMI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615072" />
        <display value="BRACHYDACTYLY, TYPE A1, C" />
      </concept>
      <concept>
        <code value="OMIM:615073" />
        <display value="DYSTONIA 25" />
      </concept>
      <concept>
        <code value="OMIM:615074" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 18" />
      </concept>
      <concept>
        <code value="OMIM:615075" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 19" />
      </concept>
      <concept>
        <code value="OMIM:615080" />
        <display value="ALZHEIMER DISEASE 17" />
      </concept>
      <concept>
        <code value="OMIM:615081" />
        <display value="SPERMATOGENIC FAILURE 11" />
      </concept>
      <concept>
        <code value="OMIM:615082" />
        <display value="C3HEX, ABILITY TO SMELL" />
      </concept>
      <concept>
        <code value="OMIM:615083" />
        <display value="COLORECTAL CANCER, SUSCEPTIBILITY TO, 12" />
      </concept>
      <concept>
        <code value="OMIM:615084" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 11" />
      </concept>
      <concept>
        <code value="OMIM:615085" />
        <display value="OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8" />
      </concept>
      <concept>
        <code value="OMIM:615091" />
        <display value="AUTISM, SUSCEPTIBILITY TO, 19" />
      </concept>
      <concept>
        <code value="OMIM:615092" />
        <display value="LEFT VENTRICULAR NONCOMPACTION 7" />
      </concept>
      <concept>
        <code value="OMIM:615095" />
        <display value="MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615102" />
        <display value="TYSHCHENKO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615107" />
        <display value="COWDEN SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:615108" />
        <display value="COWDEN SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:615109" />
        <display value="COWDEN SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:615112" />
        <display value="UROFACIAL SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:615113" />
        <display value="MICROPHTHALMIA, ISOLATED 8" />
      </concept>
      <concept>
        <code value="OMIM:615119" />
        <display value="CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2" />
      </concept>
      <concept>
        <code value="OMIM:615120" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 8" />
      </concept>
      <concept>
        <code value="OMIM:615121" />
        <display value="STOMATIN-LIKE PROTEIN-2, HYPERPHOSPHORYLATION OF" />
      </concept>
      <concept>
        <code value="OMIM:615122" />
        <display value="LYMPHOPROLIFERATIVE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:615127" />
        <display value="EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4" />
      </concept>
      <concept>
        <code value="OMIM:615134" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 9" />
      </concept>
      <concept>
        <code value="OMIM:615135" />
        <display value="MAPLE SYRUP URINE DISEASE, MILD VARIANT" />
      </concept>
      <concept>
        <code value="OMIM:615139" />
        <display value="FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE" />
      </concept>
      <concept>
        <code value="OMIM:615145" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9" />
      </concept>
      <concept>
        <code value="OMIM:615147" />
        <display value="RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615155" />
        <display value="STEEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615156" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 6" />
      </concept>
      <concept>
        <code value="OMIM:615157" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:615158" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3" />
      </concept>
      <concept>
        <code value="OMIM:615159" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:615160" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:615162" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35" />
      </concept>
      <concept>
        <code value="OMIM:615163" />
        <display value="CONE-ROD DYSTROPHY 17" />
      </concept>
      <concept>
        <code value="OMIM:615170" />
        <display value="WAHAB SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615174" />
        <display value="L-THREONINE DEHYDROGENASE, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:615179" />
        <display value="ALBINISM, OCULOCUTANEOUS, TYPE VII" />
      </concept>
      <concept>
        <code value="OMIM:615181" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11" />
      </concept>
      <concept>
        <code value="OMIM:615182" />
        <display value="COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA" />
      </concept>
      <concept>
        <code value="OMIM:615184" />
        <display value="CARDIOMYOPATHY, DILATED, 1II" />
      </concept>
      <concept>
        <code value="OMIM:615185" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F" />
      </concept>
      <concept>
        <code value="OMIM:615188" />
        <display value="CATARACT 39, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:615190" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5" />
      </concept>
      <concept>
        <code value="OMIM:615191" />
        <display value="LISSENCEPHALY 5" />
      </concept>
      <concept>
        <code value="OMIM:615192" />
        <display value="BIRTH WEIGHT QUANTITATIVE TRAIT LOCUS 4" />
      </concept>
      <concept>
        <code value="OMIM:615193" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 15" />
      </concept>
      <concept>
        <code value="OMIM:615197" />
        <display value="RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:615198" />
        <display value="OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:615206" />
        <display value="IMMUNODEFICIENCY 11" />
      </concept>
      <concept>
        <code value="OMIM:615207" />
        <display value="IMMUNODEFICIENCY 56" />
      </concept>
      <concept>
        <code value="OMIM:615214" />
        <display value="AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615217" />
        <display value="ATAXIA-OCULOMOTOR APRAXIA 3" />
      </concept>
      <concept>
        <code value="OMIM:615219" />
        <display value="HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:615220" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XV" />
      </concept>
      <concept>
        <code value="OMIM:615221" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 16" />
      </concept>
      <concept>
        <code value="OMIM:615222" />
        <display value="SMITH-MCCORT DYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:615224" />
        <display value="ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:615225" />
        <display value="PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING" />
      </concept>
      <concept>
        <code value="OMIM:615226" />
        <display value="POLYDACTYLY, POSTAXIAL, TYPE A6" />
      </concept>
      <concept>
        <code value="OMIM:615228" />
        <display value="MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4" />
      </concept>
      <concept>
        <code value="OMIM:615232" />
        <display value="SCHIZOPHRENIA 18" />
      </concept>
      <concept>
        <code value="OMIM:615233" />
        <display value="RETINITIS PIGMENTOSA 66" />
      </concept>
      <concept>
        <code value="OMIM:615234" />
        <display value="ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2" />
      </concept>
      <concept>
        <code value="OMIM:615235" />
        <display value="CARDIOMYOPATHY, DILATED, 1JJ" />
      </concept>
      <concept>
        <code value="OMIM:615236" />
        <display value="WOODS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615237" />
        <display value="CONGENITAL SHORT BOWEL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615238" />
        <display value="LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:615244" />
        <display value="NEPHROTIC SYNDROME, TYPE 8" />
      </concept>
      <concept>
        <code value="OMIM:615248" />
        <display value="CARDIOMYOPATHY, DILATED, 1KK" />
      </concept>
      <concept>
        <code value="OMIM:615249" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12" />
      </concept>
      <concept>
        <code value="OMIM:615264" />
        <display value="BLOOD GROUP, VEL SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:615266" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:615267" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:615268" />
        <display value="CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:615269" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:615270" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:615271" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:615272" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP Q" />
      </concept>
      <concept>
        <code value="OMIM:615273" />
        <display value="CONGENITAL DISORDER OF DEGLYCOSYLATION" />
      </concept>
      <concept>
        <code value="OMIM:615274" />
        <display value="CATARACT 15, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:615277" />
        <display value="CATARACT 19, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:615278" />
        <display value="CARDIOFACIOCUTANEOUS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:615279" />
        <display value="CARDIOFACIOCUTANEOUS SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:615280" />
        <display value="CARDIOFACIOCUTANEOUS SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:615281" />
        <display value="HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY" />
      </concept>
      <concept>
        <code value="OMIM:615282" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2" />
      </concept>
      <concept>
        <code value="OMIM:615284" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3" />
      </concept>
      <concept>
        <code value="OMIM:615285" />
        <display value="NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615286" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36" />
      </concept>
      <concept>
        <code value="OMIM:615287" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13" />
      </concept>
      <concept>
        <code value="OMIM:615290" />
        <display value="SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:615293" />
        <display value="MYOFIBROMATOSIS, INFANTILE, 2" />
      </concept>
      <concept>
        <code value="OMIM:615294" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 21" />
      </concept>
      <concept>
        <code value="OMIM:615297" />
        <display value="ADAMS-OLIVER SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:615298" />
        <display value="SYMPHALANGISM, PROXIMAL, 1B" />
      </concept>
      <concept>
        <code value="OMIM:615300" />
        <display value="PERRAULT SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:615311" />
        <display value="BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 17" />
      </concept>
      <concept>
        <code value="OMIM:615312" />
        <display value="ALBINISM, OCULOCUTANEOUS, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:615314" />
        <display value="CRANIOSYNOSTOSIS 3" />
      </concept>
      <concept>
        <code value="OMIM:615327" />
        <display value="DOWLING-DEGOS DISEASE 2" />
      </concept>
      <concept>
        <code value="OMIM:615328" />
        <display value="SHAHEEN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615330" />
        <display value="MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:615338" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16" />
      </concept>
      <concept>
        <code value="OMIM:615342" />
        <display value="PULMONARY HYPERTENSION, PRIMARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:615343" />
        <display value="PULMONARY HYPERTENSION, PRIMARY, 3" />
      </concept>
      <concept>
        <code value="OMIM:615344" />
        <display value="PULMONARY HYPERTENSION, PRIMARY, 4" />
      </concept>
      <concept>
        <code value="OMIM:615346" />
        <display value="PRECOCIOUS PUBERTY, CENTRAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:615348" />
        <display value="NEMALINE MYOPATHY 8" />
      </concept>
      <concept>
        <code value="OMIM:615349" />
        <display value="EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2" />
      </concept>
      <concept>
        <code value="OMIM:615350" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14" />
      </concept>
      <concept>
        <code value="OMIM:615351" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14" />
      </concept>
      <concept>
        <code value="OMIM:615352" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14" />
      </concept>
      <concept>
        <code value="OMIM:615355" />
        <display value="NOONAN SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:615356" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 18" />
      </concept>
      <concept>
        <code value="OMIM:615360" />
        <display value="LEBER CONGENITAL AMAUROSIS 17" />
      </concept>
      <concept>
        <code value="OMIM:615361" />
        <display value="HYPOCALCEMIA, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:615362" />
        <display value="CEROID LIPOFUSCINOSIS, NEURONAL, 13" />
      </concept>
      <concept>
        <code value="OMIM:615363" />
        <display value="ESTROGEN RESISTANCE" />
      </concept>
      <concept>
        <code value="OMIM:615368" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:615369" />
        <display value="EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:615371" />
        <display value="PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:615373" />
        <display value="LEFT VENTRICULAR NONCOMPACTION 8" />
      </concept>
      <concept>
        <code value="OMIM:615374" />
        <display value="CONE-ROD DYSTROPHY 18" />
      </concept>
      <concept>
        <code value="OMIM:615376" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C" />
      </concept>
      <concept>
        <code value="OMIM:615377" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 13" />
      </concept>
      <concept>
        <code value="OMIM:615378" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 14" />
      </concept>
      <concept>
        <code value="OMIM:615381" />
        <display value="MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615382" />
        <display value="NEPHRONOPHTHISIS 16" />
      </concept>
      <concept>
        <code value="OMIM:615386" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14" />
      </concept>
      <concept>
        <code value="OMIM:615387" />
        <display value="T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615390" />
        <display value="VESICOURETERAL REFLUX 7" />
      </concept>
      <concept>
        <code value="OMIM:615395" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16" />
      </concept>
      <concept>
        <code value="OMIM:615396" />
        <display value="LEFT VENTRICULAR NONCOMPACTION 10" />
      </concept>
      <concept>
        <code value="OMIM:615397" />
        <display value="MECKEL SYNDROME, TYPE 11" />
      </concept>
      <concept>
        <code value="OMIM:615398" />
        <display value="MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:615399" />
        <display value="PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2" />
      </concept>
      <concept>
        <code value="OMIM:615400" />
        <display value="EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5" />
      </concept>
      <concept>
        <code value="OMIM:615401" />
        <display value="IMMUNODEFICIENCY 8" />
      </concept>
      <concept>
        <code value="OMIM:615402" />
        <display value="DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3" />
      </concept>
      <concept>
        <code value="OMIM:615411" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3" />
      </concept>
      <concept>
        <code value="OMIM:615412" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4" />
      </concept>
      <concept>
        <code value="OMIM:615413" />
        <display value="SPERMATOGENIC FAILURE 12" />
      </concept>
      <concept>
        <code value="OMIM:615414" />
        <display value="MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615415" />
        <display value="RENAL-HEPATIC-PANCREATIC DYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:615418" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615419" />
        <display value="HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1" />
      </concept>
      <concept>
        <code value="OMIM:615420" />
        <display value="MYOPIA 22, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:615422" />
        <display value="INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2" />
      </concept>
      <concept>
        <code value="OMIM:615424" />
        <display value="INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3" />
      </concept>
      <concept>
        <code value="OMIM:615425" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:615426" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 20" />
      </concept>
      <concept>
        <code value="OMIM:615429" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 88" />
      </concept>
      <concept>
        <code value="OMIM:615431" />
        <display value="MYOPIA 23, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615432" />
        <display value="SPECIFIC LANGUAGE IMPAIRMENT 5" />
      </concept>
      <concept>
        <code value="OMIM:615433" />
        <display value="CHROMOSOME 3q13.31 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615434" />
        <display value="RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS" />
      </concept>
      <concept>
        <code value="OMIM:615436" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 8" />
      </concept>
      <concept>
        <code value="OMIM:615438" />
        <display value="INFANTILE LIVER FAILURE SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:615439" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 13" />
      </concept>
      <concept>
        <code value="OMIM:615440" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17" />
      </concept>
      <concept>
        <code value="OMIM:615441" />
        <display value="VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS" />
      </concept>
      <concept>
        <code value="OMIM:615444" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 22" />
      </concept>
      <concept>
        <code value="OMIM:615451" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 23" />
      </concept>
      <concept>
        <code value="OMIM:615453" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:615457" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18" />
      </concept>
      <concept>
        <code value="OMIM:615458" />
        <display value="MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS" />
      </concept>
      <concept>
        <code value="OMIM:615465" />
        <display value="HARTSFIELD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615468" />
        <display value="IMMUNODEFICIENCY 12" />
      </concept>
      <concept>
        <code value="OMIM:615471" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:615473" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17" />
      </concept>
      <concept>
        <code value="OMIM:615474" />
        <display value="PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:615476" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18" />
      </concept>
      <concept>
        <code value="OMIM:615481" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 24" />
      </concept>
      <concept>
        <code value="OMIM:615482" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 25" />
      </concept>
      <concept>
        <code value="OMIM:615483" />
        <display value="BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5" />
      </concept>
      <concept>
        <code value="OMIM:615485" />
        <display value="BAINBRIDGE-ROPERS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615486" />
        <display value="INTERSTITIAL LUNG AND LIVER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:615489" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 14" />
      </concept>
      <concept>
        <code value="OMIM:615490" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R" />
      </concept>
      <concept>
        <code value="OMIM:615491" />
        <display value="SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615493" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37" />
      </concept>
      <concept>
        <code value="OMIM:615500" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 26" />
      </concept>
      <concept>
        <code value="OMIM:615501" />
        <display value="MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C" />
      </concept>
      <concept>
        <code value="OMIM:615502" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 21" />
      </concept>
      <concept>
        <code value="OMIM:615503" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:615504" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 27" />
      </concept>
      <concept>
        <code value="OMIM:615505" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 28" />
      </concept>
      <concept>
        <code value="OMIM:615506" />
        <display value="TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:615508" />
        <display value="ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE" />
      </concept>
      <concept>
        <code value="OMIM:615510" />
        <display value="ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615511" />
        <display value="MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615512" />
        <display value="TRIOSEPHOSPHATE ISOMERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615513" />
        <display value="IMMUNODEFICIENCY 14" />
      </concept>
      <concept>
        <code value="OMIM:615515" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 19" />
      </concept>
      <concept>
        <code value="OMIM:615516" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38" />
      </concept>
      <concept>
        <code value="OMIM:615517" />
        <display value="HEMOCHROMATOSIS, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:615518" />
        <display value="IMMUNODEFICIENCY 13" />
      </concept>
      <concept>
        <code value="OMIM:615522" />
        <display value="COLE DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:615523" />
        <display value="CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8" />
      </concept>
      <concept>
        <code value="OMIM:615524" />
        <display value="MICROPHTHALMIA, SYNDROMIC 12" />
      </concept>
      <concept>
        <code value="OMIM:615527" />
        <display value="CANDIDIASIS, FAMILIAL, 8" />
      </concept>
      <concept>
        <code value="OMIM:615528" />
        <display value="PARKINSON DISEASE 19A, JUVENILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:615529" />
        <display value="CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:615530" />
        <display value="PARKINSON DISEASE 20, EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:615537" />
        <display value="RETICULATE ACROPIGMENTATION OF KITAMURA" />
      </concept>
      <concept>
        <code value="OMIM:615538" />
        <display value="CHROMOSOME 22q13 DUPLICATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615539" />
        <display value="EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2" />
      </concept>
      <concept>
        <code value="OMIM:615540" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 76" />
      </concept>
      <concept>
        <code value="OMIM:615541" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39" />
      </concept>
      <concept>
        <code value="OMIM:615542" />
        <display value="TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:615544" />
        <display value="PERIVENTRICULAR NODULAR HETEROTOPIA 6" />
      </concept>
      <concept>
        <code value="OMIM:615545" />
        <display value="LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:615546" />
        <display value="VAN MALDERGEM SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:615547" />
        <display value="SCHAAF-YANG SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615548" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII" />
      </concept>
      <concept>
        <code value="OMIM:615550" />
        <display value="DIAMOND-BLACKFAN ANEMIA 12" />
      </concept>
      <concept>
        <code value="OMIM:615551" />
        <display value="EPISODIC PAIN SYNDROME, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:615552" />
        <display value="EPISODIC PAIN SYNDROME, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:615553" />
        <display value="ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:615554" />
        <display value="MULTIPLE FIBROADENOMAS OF THE BREAST" />
      </concept>
      <concept>
        <code value="OMIM:615555" />
        <display value="HYPERPROLACTINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:615557" />
        <display value="MELIOIDOSIS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:615558" />
        <display value="HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1" />
      </concept>
      <concept>
        <code value="OMIM:615559" />
        <display value="AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:615560" />
        <display value="OTOFACIOCERVICAL SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:615561" />
        <display value="COMPLEMENT FACTOR B DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615565" />
        <display value="RETINITIS PIGMENTOSA 67" />
      </concept>
      <concept>
        <code value="OMIM:615573" />
        <display value="NEPHROTIC SYNDROME, TYPE 9" />
      </concept>
      <concept>
        <code value="OMIM:615574" />
        <display value="ASPARAGINE SYNTHETASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615575" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID" />
      </concept>
      <concept>
        <code value="OMIM:615577" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 10" />
      </concept>
      <concept>
        <code value="OMIM:615578" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18" />
      </concept>
      <concept>
        <code value="OMIM:615582" />
        <display value="LOEYS-DIETZ SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:615583" />
        <display value="VERHEIJ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615589" />
        <display value="OTOSCLEROSIS 10" />
      </concept>
      <concept>
        <code value="OMIM:615590" />
        <display value="ALZHEIMER DISEASE 18" />
      </concept>
      <concept>
        <code value="OMIM:615591" />
        <display value="MACULAR DEGENERATION, AGE-RELATED, 15" />
      </concept>
      <concept>
        <code value="OMIM:615592" />
        <display value="IMMUNODEFICIENCY 15" />
      </concept>
      <concept>
        <code value="OMIM:615593" />
        <display value="IMMUNODEFICIENCY 16" />
      </concept>
      <concept>
        <code value="OMIM:615595" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19" />
      </concept>
      <concept>
        <code value="OMIM:615596" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw" />
      </concept>
      <concept>
        <code value="OMIM:615597" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix" />
      </concept>
      <concept>
        <code value="OMIM:615598" />
        <display value="PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:615599" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40" />
      </concept>
      <concept>
        <code value="OMIM:615602" />
        <display value="MEMORY QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:615604" />
        <display value="L-FERRITIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615605" />
        <display value="FANCONI RENOTUBULAR SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:615607" />
        <display value="IMMUNODEFICIENCY 17" />
      </concept>
      <concept>
        <code value="OMIM:615612" />
        <display value="DEVELOPMENTAL DYSPLASIA OF THE HIP 2" />
      </concept>
      <concept>
        <code value="OMIM:615615" />
        <display value="IMMUNODEFICIENCY 18" />
      </concept>
      <concept>
        <code value="OMIM:615616" />
        <display value="ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13" />
      </concept>
      <concept>
        <code value="OMIM:615617" />
        <display value="IMMUNODEFICIENCY 19" />
      </concept>
      <concept>
        <code value="OMIM:615619" />
        <display value="CHOLANGIOCARCINOMA, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:615625" />
        <display value="SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615629" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 56" />
      </concept>
      <concept>
        <code value="OMIM:615630" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:615631" />
        <display value="ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib" />
      </concept>
      <concept>
        <code value="OMIM:615632" />
        <display value="NEUROPATHY, HEREDITARY SENSORY, TYPE IF" />
      </concept>
      <concept>
        <code value="OMIM:615633" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:615636" />
        <display value="JOUBERT SYNDROME 21" />
      </concept>
      <concept>
        <code value="OMIM:615637" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41" />
      </concept>
      <concept>
        <code value="OMIM:615643" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6" />
      </concept>
      <concept>
        <code value="OMIM:615649" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 54" />
      </concept>
      <concept>
        <code value="OMIM:615651" />
        <display value="LEUKOENCEPHALOPATHY WITH ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:615654" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 58" />
      </concept>
      <concept>
        <code value="OMIM:615656" />
        <display value="CHROMOSOME 15q11.2 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615658" />
        <display value="SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615663" />
        <display value="WARBURG MICRO SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:615665" />
        <display value="JOUBERT SYNDROME 22" />
      </concept>
      <concept>
        <code value="OMIM:615668" />
        <display value="CHROMOSOME 5q12 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615670" />
        <display value="SCHWANNOMATOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:615673" />
        <display value="MYOPATHY WITH EXTRAPYRAMIDAL SIGNS" />
      </concept>
      <concept>
        <code value="OMIM:615674" />
        <display value="DOWLING-DEGOS DISEASE 3" />
      </concept>
      <concept>
        <code value="OMIM:615681" />
        <display value="SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615683" />
        <display value="SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615685" />
        <display value="SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615686" />
        <display value="SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615688" />
        <display value="POLYARTERITIS NODOSA, CHILDHOOD-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:615696" />
        <display value="DOWLING-DEGOS DISEASE 4" />
      </concept>
      <concept>
        <code value="OMIM:615697" />
        <display value="EPILEPSY, FAMILIAL TEMPORAL LOBE, 6" />
      </concept>
      <concept>
        <code value="OMIM:615703" />
        <display value="MORBID OBESITY AND SPERMATOGENIC FAILURE" />
      </concept>
      <concept>
        <code value="OMIM:615704" />
        <display value="POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS" />
      </concept>
      <concept>
        <code value="OMIM:615705" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15" />
      </concept>
      <concept>
        <code value="OMIM:615706" />
        <display value="AURICULOCONDYLAR SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:615707" />
        <display value="IMMUNODEFICIENCY 20" />
      </concept>
      <concept>
        <code value="OMIM:615709" />
        <display value="SACRAL AGENESIS WITH VERTEBRAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:615710" />
        <display value="MITCHELL-RILEY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615711" />
        <display value="ALZHEIMER DISEASE 19" />
      </concept>
      <concept>
        <code value="OMIM:615715" />
        <display value="BONE MARROW FAILURE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:615716" />
        <display value="HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:615721" />
        <display value="RENAL HYPODYSPLASIA/APLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:615722" />
        <display value="BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615723" />
        <display value="PREMATURE OVARIAN FAILURE 8" />
      </concept>
      <concept>
        <code value="OMIM:615724" />
        <display value="PREMATURE OVARIAN FAILURE 9" />
      </concept>
      <concept>
        <code value="OMIM:615725" />
        <display value="RETINITIS PIGMENTOSA 68" />
      </concept>
      <concept>
        <code value="OMIM:615726" />
        <display value="PACHYONYCHIA CONGENITA 3" />
      </concept>
      <concept>
        <code value="OMIM:615728" />
        <display value="PACHYONYCHIA CONGENITA 4" />
      </concept>
      <concept>
        <code value="OMIM:615731" />
        <display value="NEMALINE MYOPATHY 9" />
      </concept>
      <concept>
        <code value="OMIM:615735" />
        <display value="PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE" />
      </concept>
      <concept>
        <code value="OMIM:615744" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19" />
      </concept>
      <concept>
        <code value="OMIM:615745" />
        <display value="ATRIAL STANDSTILL 2" />
      </concept>
      <concept>
        <code value="OMIM:615749" />
        <display value="ECULIZUMAB, POOR RESPONSE TO" />
      </concept>
      <concept>
        <code value="OMIM:615750" />
        <display value="MOYAMOYA DISEASE 6 WITH OR WITHOUT ACHALASIA" />
      </concept>
      <concept>
        <code value="OMIM:615751" />
        <display value="CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO" />
      </concept>
      <concept>
        <code value="OMIM:615752" />
        <display value="POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:615758" />
        <display value="IMMUNODEFICIENCY 22" />
      </concept>
      <concept>
        <code value="OMIM:615760" />
        <display value="MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:615761" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 23" />
      </concept>
      <concept>
        <code value="OMIM:615763" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5" />
      </concept>
      <concept>
        <code value="OMIM:615767" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 11" />
      </concept>
      <concept>
        <code value="OMIM:615768" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16" />
      </concept>
      <concept>
        <code value="OMIM:615770" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 15" />
      </concept>
      <concept>
        <code value="OMIM:615771" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6" />
      </concept>
      <concept>
        <code value="OMIM:615774" />
        <display value="OOCYTE MATURATION DEFECT 1" />
      </concept>
      <concept>
        <code value="OMIM:615777" />
        <display value="DESBUQUOIS DYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:615779" />
        <display value="CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4" />
      </concept>
      <concept>
        <code value="OMIM:615780" />
        <display value="RETINITIS PIGMENTOSA 69" />
      </concept>
      <concept>
        <code value="OMIM:615785" />
        <display value="WHITE SPONGE NEVUS 2" />
      </concept>
      <concept>
        <code value="OMIM:615789" />
        <display value="SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES" />
      </concept>
      <concept>
        <code value="OMIM:615802" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42" />
      </concept>
      <concept>
        <code value="OMIM:615803" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 10" />
      </concept>
      <concept>
        <code value="OMIM:615807" />
        <display value="SECKEL SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:615809" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 9" />
      </concept>
      <concept>
        <code value="OMIM:615812" />
        <display value="ABDOMINAL OBESITY-METABOLIC SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:615816" />
        <display value="IMMUNODEFICIENCY 23" />
      </concept>
      <concept>
        <code value="OMIM:615817" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43" />
      </concept>
      <concept>
        <code value="OMIM:615821" />
        <display value="CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS" />
      </concept>
      <concept>
        <code value="OMIM:615824" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7" />
      </concept>
      <concept>
        <code value="OMIM:615828" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 24" />
      </concept>
      <concept>
        <code value="OMIM:615829" />
        <display value="XIA-GIBBS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615830" />
        <display value="PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4" />
      </concept>
      <concept>
        <code value="OMIM:615833" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21" />
      </concept>
      <concept>
        <code value="OMIM:615834" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 26" />
      </concept>
      <concept>
        <code value="OMIM:615835" />
        <display value="CHROMOSOME 16 INVERSION, 0.45-MB" />
      </concept>
      <concept>
        <code value="OMIM:615837" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 101" />
      </concept>
      <concept>
        <code value="OMIM:615838" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8" />
      </concept>
      <concept>
        <code value="OMIM:615841" />
        <display value="SPERMATOGENIC FAILURE 13" />
      </concept>
      <concept>
        <code value="OMIM:615842" />
        <display value="SPERMATOGENIC FAILURE 14" />
      </concept>
      <concept>
        <code value="OMIM:615846" />
        <display value="AICARDI-GOUTIERES SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:615848" />
        <display value="MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10" />
      </concept>
      <concept>
        <code value="OMIM:615849" />
        <display value="CULLER-JONES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615851" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 2E" />
      </concept>
      <concept>
        <code value="OMIM:615859" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23" />
      </concept>
      <concept>
        <code value="OMIM:615860" />
        <display value="CONE-ROD DYSTROPHY 19" />
      </concept>
      <concept>
        <code value="OMIM:615861" />
        <display value="NEPHROTIC SYNDROME, TYPE 10" />
      </concept>
      <concept>
        <code value="OMIM:615862" />
        <display value="NEPHRONOPHTHISIS 18" />
      </concept>
      <concept>
        <code value="OMIM:615863" />
        <display value="DIARRHEA 7, PROTEIN-LOSING ENTEROPATHY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:615866" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 27" />
      </concept>
      <concept>
        <code value="OMIM:615871" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24" />
      </concept>
      <concept>
        <code value="OMIM:615872" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 29" />
      </concept>
      <concept>
        <code value="OMIM:615873" />
        <display value="HELSMOORTEL-VAN DER AA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615877" />
        <display value="MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615878" />
        <display value="CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4" />
      </concept>
      <concept>
        <code value="OMIM:615879" />
        <display value="TATTON-BROWN-RAHMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615881" />
        <display value="PLASMA TRIGLYCERIDE LEVEL QUANTITATIVE TRAIT LOCUS" />
      </concept>
      <concept>
        <code value="OMIM:615883" />
        <display value="MYOPATHY, TUBULAR AGGREGATE, 2" />
      </concept>
      <concept>
        <code value="OMIM:615885" />
        <display value="HYPOTRICHOSIS 12" />
      </concept>
      <concept>
        <code value="OMIM:615887" />
        <display value="AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5" />
      </concept>
      <concept>
        <code value="OMIM:615888" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 18" />
      </concept>
      <concept>
        <code value="OMIM:615889" />
        <display value="LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE" />
      </concept>
      <concept>
        <code value="OMIM:615892" />
        <display value="OROFACIAL CLEFT 14" />
      </concept>
      <concept>
        <code value="OMIM:615895" />
        <display value="POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615896" />
        <display value="HYPOTRICHOSIS 13" />
      </concept>
      <concept>
        <code value="OMIM:615897" />
        <display value="IMMUNODEFICIENCY 24" />
      </concept>
      <concept>
        <code value="OMIM:615905" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25" />
      </concept>
      <concept>
        <code value="OMIM:615907" />
        <display value="LYMPHEDEMA, HEREDITARY, ID" />
      </concept>
      <concept>
        <code value="OMIM:615909" />
        <display value="DIAMOND-BLACKFAN ANEMIA 13" />
      </concept>
      <concept>
        <code value="OMIM:615911" />
        <display value="FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:615916" />
        <display value="CARDIOMYOPATHY, DILATED, 1NN" />
      </concept>
      <concept>
        <code value="OMIM:615917" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20" />
      </concept>
      <concept>
        <code value="OMIM:615918" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21" />
      </concept>
      <concept>
        <code value="OMIM:615919" />
        <display value="ATAXIA-TELANGIECTASIA-LIKE DISORDER 2" />
      </concept>
      <concept>
        <code value="OMIM:615922" />
        <display value="RETINITIS PIGMENTOSA 70" />
      </concept>
      <concept>
        <code value="OMIM:615923" />
        <display value="EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:615924" />
        <display value="ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:615925" />
        <display value="GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL" />
      </concept>
      <concept>
        <code value="OMIM:615926" />
        <display value="WEBB-DATTANI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615934" />
        <display value="STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:615935" />
        <display value="PANCREATIC AGENESIS 2" />
      </concept>
      <concept>
        <code value="OMIM:615937" />
        <display value="MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:615938" />
        <display value="MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:615942" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44" />
      </concept>
      <concept>
        <code value="OMIM:615945" />
        <display value="SPINOCEREBELLAR ATAXIA 37" />
      </concept>
      <concept>
        <code value="OMIM:615946" />
        <display value="MYOPIA 24, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:615947" />
        <display value="HYPERLIPOPROTEINEMIA, TYPE ID" />
      </concept>
      <concept>
        <code value="OMIM:615948" />
        <display value="OROFACIODIGITAL SYNDROME XIV" />
      </concept>
      <concept>
        <code value="OMIM:615952" />
        <display value="AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1" />
      </concept>
      <concept>
        <code value="OMIM:615953" />
        <display value="KALLIKREIN, DECREASED URINARY ACTIVITY OF" />
      </concept>
      <concept>
        <code value="OMIM:615954" />
        <display value="ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:615957" />
        <display value="SPINOCEREBELLAR ATAXIA 38" />
      </concept>
      <concept>
        <code value="OMIM:615959" />
        <display value="MYOPATHY, CENTRONUCLEAR, 5" />
      </concept>
      <concept>
        <code value="OMIM:615960" />
        <display value="PORETTI-BOLTSHAUSER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:615961" />
        <display value="ACID-LABILE SUBUNIT DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615962" />
        <display value="GLUCOCORTICOID RESISTANCE, GENERALIZED" />
      </concept>
      <concept>
        <code value="OMIM:615963" />
        <display value="VESICOURETERAL REFLUX 8" />
      </concept>
      <concept>
        <code value="OMIM:615966" />
        <display value="IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:615969" />
        <display value="ALPHA-FETOPROTEIN DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:615970" />
        <display value="ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF" />
      </concept>
      <concept>
        <code value="OMIM:615972" />
        <display value="NANOPHTHALMOS 4" />
      </concept>
      <concept>
        <code value="OMIM:615973" />
        <display value="CONE-ROD DYSTROPHY 20" />
      </concept>
      <concept>
        <code value="OMIM:615974" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 102" />
      </concept>
      <concept>
        <code value="OMIM:615978" />
        <display value="IMMUNODEFICIENCY 27B" />
      </concept>
      <concept>
        <code value="OMIM:615979" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45" />
      </concept>
      <concept>
        <code value="OMIM:615980" />
        <display value="LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6" />
      </concept>
      <concept>
        <code value="OMIM:615981" />
        <display value="BARDET-BIEDL SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:615982" />
        <display value="BARDET-BIEDL SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:615983" />
        <display value="BARDET-BIEDL SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:615984" />
        <display value="BARDET-BIEDL SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:615985" />
        <display value="BARDET-BIEDL SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:615986" />
        <display value="BARDET-BIEDL SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:615987" />
        <display value="BARDET-BIEDL SYNDROME 10" />
      </concept>
      <concept>
        <code value="OMIM:615988" />
        <display value="BARDET-BIEDL SYNDROME 11" />
      </concept>
      <concept>
        <code value="OMIM:615989" />
        <display value="BARDET-BIEDL SYNDROME 12" />
      </concept>
      <concept>
        <code value="OMIM:615990" />
        <display value="BARDET-BIEDL SYNDROME 13" />
      </concept>
      <concept>
        <code value="OMIM:615991" />
        <display value="BARDET-BIEDL SYNDROME 14" />
      </concept>
      <concept>
        <code value="OMIM:615992" />
        <display value="BARDET-BIEDL SYNDROME 15" />
      </concept>
      <concept>
        <code value="OMIM:615993" />
        <display value="BARDET-BIEDL SYNDROME 16" />
      </concept>
      <concept>
        <code value="OMIM:615994" />
        <display value="BARDET-BIEDL SYNDROME 17" />
      </concept>
      <concept>
        <code value="OMIM:615995" />
        <display value="BARDET-BIEDL SYNDROME 18" />
      </concept>
      <concept>
        <code value="OMIM:615996" />
        <display value="BARDET-BIEDL SYNDROME 19" />
      </concept>
      <concept>
        <code value="OMIM:615999" />
        <display value="HYPERTHYROXINEMIA, FAMILIAL DYSALBUMINEMIC" />
      </concept>
      <concept>
        <code value="OMIM:616000" />
        <display value="ANALBUMINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:616001" />
        <display value="BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2" />
      </concept>
      <concept>
        <code value="OMIM:616002" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7" />
      </concept>
      <concept>
        <code value="OMIM:616004" />
        <display value="DYSFIBRINOGENEMIA, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:616005" />
        <display value="IMMUNODEFICIENCY 36" />
      </concept>
      <concept>
        <code value="OMIM:616006" />
        <display value="HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:616007" />
        <display value="CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:616022" />
        <display value="NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616025" />
        <display value="GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11" />
      </concept>
      <concept>
        <code value="OMIM:616026" />
        <display value="FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG" />
      </concept>
      <concept>
        <code value="OMIM:616028" />
        <display value="ADAMS-OLIVER SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:616029" />
        <display value="ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616030" />
        <display value="HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA" />
      </concept>
      <concept>
        <code value="OMIM:616032" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8" />
      </concept>
      <concept>
        <code value="OMIM:616033" />
        <display value="MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1" />
      </concept>
      <concept>
        <code value="OMIM:616034" />
        <display value="2,4-DIENOYL-CoA REDUCTASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:616037" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 30" />
      </concept>
      <concept>
        <code value="OMIM:616038" />
        <display value="NEU-LAXOVA SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:616039" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D" />
      </concept>
      <concept>
        <code value="OMIM:616040" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC" />
      </concept>
      <concept>
        <code value="OMIM:616042" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 103" />
      </concept>
      <concept>
        <code value="OMIM:616044" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 65" />
      </concept>
      <concept>
        <code value="OMIM:616045" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22" />
      </concept>
      <concept>
        <code value="OMIM:616050" />
        <display value="AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS" />
      </concept>
      <concept>
        <code value="OMIM:616051" />
        <display value="MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616052" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7" />
      </concept>
      <concept>
        <code value="OMIM:616053" />
        <display value="SPINOCEREBELLAR ATAXIA 40" />
      </concept>
      <concept>
        <code value="OMIM:616055" />
        <display value="EPISODIC ATAXIA, TYPE 8" />
      </concept>
      <concept>
        <code value="OMIM:616056" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26" />
      </concept>
      <concept>
        <code value="OMIM:616059" />
        <display value="MIRROR MOVEMENTS 3" />
      </concept>
      <concept>
        <code value="OMIM:616060" />
        <display value="BLOOD GROUP, DOMBROCK SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:616063" />
        <display value="POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE" />
      </concept>
      <concept>
        <code value="OMIM:616067" />
        <display value="46,XY SEX REVERSAL 9" />
      </concept>
      <concept>
        <code value="OMIM:616069" />
        <display value="INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:616078" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 29" />
      </concept>
      <concept>
        <code value="OMIM:616079" />
        <display value="RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:616080" />
        <display value="MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616081" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 1C" />
      </concept>
      <concept>
        <code value="OMIM:616083" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 30" />
      </concept>
      <concept>
        <code value="OMIM:616084" />
        <display value="SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:616087" />
        <display value="DIABETES MELLITUS, NONINSULIN-DEPENDENT, 5" />
      </concept>
      <concept>
        <code value="OMIM:616089" />
        <display value="BLOOD GROUP, GERBICH SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:616093" />
        <display value="BLOOD GROUP, ABO SYSTEM" />
      </concept>
      <concept>
        <code value="OMIM:616094" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12" />
      </concept>
      <concept>
        <code value="OMIM:616095" />
        <display value="MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:616098" />
        <display value="IMMUNODEFICIENCY 37" />
      </concept>
      <concept>
        <code value="OMIM:616099" />
        <display value="PALMOPLANTAR KERATODERMA AND WOOLLY HAIR" />
      </concept>
      <concept>
        <code value="OMIM:616100" />
        <display value="AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:616106" />
        <display value="PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:616108" />
        <display value="RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616111" />
        <display value="MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9" />
      </concept>
      <concept>
        <code value="OMIM:616113" />
        <display value="POLYENDOCRINE-POLYNEUROPATHY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616115" />
        <display value="FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:616116" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46" />
      </concept>
      <concept>
        <code value="OMIM:616117" />
        <display value="CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:616118" />
        <display value="MACULAR DEGENERATION, EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:616121" />
        <display value="GTPase, VERY LARGE INTERFERON-INDUCIBLE, PSEUDOGENE 1" />
      </concept>
      <concept>
        <code value="OMIM:616126" />
        <display value="IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION" />
      </concept>
      <concept>
        <code value="OMIM:616127" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17" />
      </concept>
      <concept>
        <code value="OMIM:616138" />
        <display value="PERRAULT SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:616139" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27" />
      </concept>
      <concept>
        <code value="OMIM:616140" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 9" />
      </concept>
      <concept>
        <code value="OMIM:616145" />
        <display value="CATEL-MANZKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616151" />
        <display value="MACULAR DYSTROPHY, VITELLIFORM, 4" />
      </concept>
      <concept>
        <code value="OMIM:616152" />
        <display value="MACULAR DYSTROPHY, VITELLIFORM, 5" />
      </concept>
      <concept>
        <code value="OMIM:616154" />
        <display value="PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:616155" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S" />
      </concept>
      <concept>
        <code value="OMIM:616158" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 31" />
      </concept>
      <concept>
        <code value="OMIM:616165" />
        <display value="NEMALINE MYOPATHY 10" />
      </concept>
      <concept>
        <code value="OMIM:616166" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 9" />
      </concept>
      <concept>
        <code value="OMIM:616170" />
        <display value="MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT" />
      </concept>
      <concept>
        <code value="OMIM:616171" />
        <display value="MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2" />
      </concept>
      <concept>
        <code value="OMIM:616172" />
        <display value="GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9" />
      </concept>
      <concept>
        <code value="OMIM:616176" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 19" />
      </concept>
      <concept>
        <code value="OMIM:616182" />
        <display value="CHRONIC MOUNTAIN SICKNESS, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:616185" />
        <display value="OVARIAN DYSGENESIS 4" />
      </concept>
      <concept>
        <code value="OMIM:616187" />
        <display value="EPILEPSY, PROGRESSIVE MYOCLONIC 7" />
      </concept>
      <concept>
        <code value="OMIM:616188" />
        <display value="RETINAL DYSTROPHY AND OBESITY" />
      </concept>
      <concept>
        <code value="OMIM:616192" />
        <display value="ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS" />
      </concept>
      <concept>
        <code value="OMIM:616193" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47" />
      </concept>
      <concept>
        <code value="OMIM:616198" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23" />
      </concept>
      <concept>
        <code value="OMIM:616199" />
        <display value="POLYGLUCOSAN BODY MYOPATHY 2" />
      </concept>
      <concept>
        <code value="OMIM:616200" />
        <display value="RUIJS-AALFS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616201" />
        <display value="CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA" />
      </concept>
      <concept>
        <code value="OMIM:616202" />
        <display value="CEREBELLOFACIODENTAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616204" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18" />
      </concept>
      <concept>
        <code value="OMIM:616208" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA" />
      </concept>
      <concept>
        <code value="OMIM:616209" />
        <display value="MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:616211" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28" />
      </concept>
      <concept>
        <code value="OMIM:616212" />
        <display value="LISSENCEPHALY 6 WITH MICROCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:616214" />
        <display value="HYPERPROINSULINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:616216" />
        <display value="THROMBOCYTOPENIA 5" />
      </concept>
      <concept>
        <code value="OMIM:616217" />
        <display value="NEPHRONOPHTHISIS 19" />
      </concept>
      <concept>
        <code value="OMIM:616219" />
        <display value="FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:616220" />
        <display value="FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9" />
      </concept>
      <concept>
        <code value="OMIM:616221" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IH" />
      </concept>
      <concept>
        <code value="OMIM:616222" />
        <display value="TEMPLE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616224" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 22" />
      </concept>
      <concept>
        <code value="OMIM:616227" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 15" />
      </concept>
      <concept>
        <code value="OMIM:616228" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 14" />
      </concept>
      <concept>
        <code value="OMIM:616229" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XVI" />
      </concept>
      <concept>
        <code value="OMIM:616230" />
        <display value="EPILEPSY, PROGRESSIVE MYOCLONIC, 8" />
      </concept>
      <concept>
        <code value="OMIM:616231" />
        <display value="MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES" />
      </concept>
      <concept>
        <code value="OMIM:616239" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24" />
      </concept>
      <concept>
        <code value="OMIM:616247" />
        <display value="LONG QT SYNDROME 14" />
      </concept>
      <concept>
        <code value="OMIM:616248" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:616249" />
        <display value="LONG QT SYNDROME 15" />
      </concept>
      <concept>
        <code value="OMIM:616255" />
        <display value="SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:616258" />
        <display value="MECKEL SYNDROME 12" />
      </concept>
      <concept>
        <code value="OMIM:616260" />
        <display value="TENORIO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616263" />
        <display value="NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:616265" />
        <display value="PEELING SKIN SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:616266" />
        <display value="CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:616267" />
        <display value="ATAXIA-OCULOMOTOR APRAXIA 4" />
      </concept>
      <concept>
        <code value="OMIM:616268" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 32" />
      </concept>
      <concept>
        <code value="OMIM:616269" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48" />
      </concept>
      <concept>
        <code value="OMIM:616270" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IF" />
      </concept>
      <concept>
        <code value="OMIM:616271" />
        <display value="3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA" />
      </concept>
      <concept>
        <code value="OMIM:616276" />
        <display value="COENZYME Q10 DEFICIENCY, PRIMARY, 7" />
      </concept>
      <concept>
        <code value="OMIM:616277" />
        <display value="MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:616278" />
        <display value="BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:616279" />
        <display value="CATARACT 43" />
      </concept>
      <concept>
        <code value="OMIM:616280" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U" />
      </concept>
      <concept>
        <code value="OMIM:616281" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49" />
      </concept>
      <concept>
        <code value="OMIM:616282" />
        <display value="SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:616286" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:616287" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:616289" />
        <display value="OPTIC ATROPHY 9" />
      </concept>
      <concept>
        <code value="OMIM:616291" />
        <display value="LICHTENSTEIN-KNORR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616294" />
        <display value="COLE-CARPENTER SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:616295" />
        <display value="PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS" />
      </concept>
      <concept>
        <code value="OMIM:616298" />
        <display value="SINGLETON-MERTEN SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:616299" />
        <display value="LIPOYLTRANSFERASE 1 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:616300" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:616304" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 17" />
      </concept>
      <concept>
        <code value="OMIM:616307" />
        <display value="SENIOR-LOKEN SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:616311" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 33" />
      </concept>
      <concept>
        <code value="OMIM:616313" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL" />
      </concept>
      <concept>
        <code value="OMIM:616314" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:616321" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL" />
      </concept>
      <concept>
        <code value="OMIM:616322" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL" />
      </concept>
      <concept>
        <code value="OMIM:616323" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:616324" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL" />
      </concept>
      <concept>
        <code value="OMIM:616325" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:616326" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:616329" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13" />
      </concept>
      <concept>
        <code value="OMIM:616330" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 18" />
      </concept>
      <concept>
        <code value="OMIM:616331" />
        <display value="ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:616335" />
        <display value="MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3" />
      </concept>
      <concept>
        <code value="OMIM:616339" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29" />
      </concept>
      <concept>
        <code value="OMIM:616340" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 67" />
      </concept>
      <concept>
        <code value="OMIM:616341" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30" />
      </concept>
      <concept>
        <code value="OMIM:616342" />
        <display value="LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:616345" />
        <display value="IMMUNODEFICIENCY 39" />
      </concept>
      <concept>
        <code value="OMIM:616346" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31" />
      </concept>
      <concept>
        <code value="OMIM:616351" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 34" />
      </concept>
      <concept>
        <code value="OMIM:616353" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6" />
      </concept>
      <concept>
        <code value="OMIM:616354" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20" />
      </concept>
      <concept>
        <code value="OMIM:616355" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 35" />
      </concept>
      <concept>
        <code value="OMIM:616357" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 40" />
      </concept>
      <concept>
        <code value="OMIM:616361" />
        <display value="PARKINSON DISEASE 21" />
      </concept>
      <concept>
        <code value="OMIM:616362" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 36" />
      </concept>
      <concept>
        <code value="OMIM:616364" />
        <display value="WHITE-SUTTON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616366" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32" />
      </concept>
      <concept>
        <code value="OMIM:616367" />
        <display value="MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA" />
      </concept>
      <concept>
        <code value="OMIM:616368" />
        <display value="CHOPS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616370" />
        <display value="MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:616371" />
        <display value="PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4" />
      </concept>
      <concept>
        <code value="OMIM:616373" />
        <display value="PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3" />
      </concept>
      <concept>
        <code value="OMIM:616389" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G" />
      </concept>
      <concept>
        <code value="OMIM:616390" />
        <display value="TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:616392" />
        <display value="SKINT1-LIKE PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:616393" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 38" />
      </concept>
      <concept>
        <code value="OMIM:616394" />
        <display value="RETINITIS PIGMENTOSA 71" />
      </concept>
      <concept>
        <code value="OMIM:616395" />
        <display value="TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:616398" />
        <display value="DYSTONIA 26, MYOCLONIC" />
      </concept>
      <concept>
        <code value="OMIM:616399" />
        <display value="BRUGADA SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:616400" />
        <display value="PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2" />
      </concept>
      <concept>
        <code value="OMIM:616402" />
        <display value="MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616407" />
        <display value="BROWN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616409" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33" />
      </concept>
      <concept>
        <code value="OMIM:616410" />
        <display value="SPINOCEREBELLAR ATAXIA 41" />
      </concept>
      <concept>
        <code value="OMIM:616411" />
        <display value="DYSTONIA 27" />
      </concept>
      <concept>
        <code value="OMIM:616413" />
        <display value="BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6" />
      </concept>
      <concept>
        <code value="OMIM:616414" />
        <display value="AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:616415" />
        <display value="FAMILIAL ADENOMATOUS POLYPOSIS 3" />
      </concept>
      <concept>
        <code value="OMIM:616418" />
        <display value="HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:616420" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 10" />
      </concept>
      <concept>
        <code value="OMIM:616421" />
        <display value="MYOCLONIC-ATONIC EPILEPSY" />
      </concept>
      <concept>
        <code value="OMIM:616425" />
        <display value="46,XY SEX REVERSAL 10" />
      </concept>
      <concept>
        <code value="OMIM:616428" />
        <display value="MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10" />
      </concept>
      <concept>
        <code value="OMIM:616430" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25" />
      </concept>
      <concept>
        <code value="OMIM:616433" />
        <display value="IMMUNODEFICIENCY 40" />
      </concept>
      <concept>
        <code value="OMIM:616435" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP T" />
      </concept>
      <concept>
        <code value="OMIM:616436" />
        <display value="EPILEPSY, FAMILIAL TEMPORAL LOBE, 7" />
      </concept>
      <concept>
        <code value="OMIM:616437" />
        <display value="FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3" />
      </concept>
      <concept>
        <code value="OMIM:616439" />
        <display value="FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4" />
      </concept>
      <concept>
        <code value="OMIM:616445" />
        <display value="CANDIDIASIS, FAMILIAL, 9" />
      </concept>
      <concept>
        <code value="OMIM:616449" />
        <display value="BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616451" />
        <display value="SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616452" />
        <display value="B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY" />
      </concept>
      <concept>
        <code value="OMIM:616455" />
        <display value="ZIMMERMANN-LABAND SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:616457" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50" />
      </concept>
      <concept>
        <code value="OMIM:616459" />
        <display value="AL-RAQAD SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616460" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50" />
      </concept>
      <concept>
        <code value="OMIM:616461" />
        <display value="EPILEPSY, FAMILIAL TEMPORAL LOBE, 8" />
      </concept>
      <concept>
        <code value="OMIM:616462" />
        <display value="ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE" />
      </concept>
      <concept>
        <code value="OMIM:616468" />
        <display value="EXUDATIVE VITREORETINOPATHY 6" />
      </concept>
      <concept>
        <code value="OMIM:616469" />
        <display value="RETINITIS PIGMENTOSA 72" />
      </concept>
      <concept>
        <code value="OMIM:616470" />
        <display value="ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2" />
      </concept>
      <concept>
        <code value="OMIM:616471" />
        <display value="BETHLEM MYOPATHY 2" />
      </concept>
      <concept>
        <code value="OMIM:616479" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2" />
      </concept>
      <concept>
        <code value="OMIM:616481" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 32" />
      </concept>
      <concept>
        <code value="OMIM:616482" />
        <display value="ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS" />
      </concept>
      <concept>
        <code value="OMIM:616483" />
        <display value="INFANTILE LIVER FAILURE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:616486" />
        <display value="MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616487" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:616488" />
        <display value="NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII" />
      </concept>
      <concept>
        <code value="OMIM:616489" />
        <display value="GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES" />
      </concept>
      <concept>
        <code value="OMIM:616490" />
        <display value="JOUBERT SYNDROME 23" />
      </concept>
      <concept>
        <code value="OMIM:616491" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V" />
      </concept>
      <concept>
        <code value="OMIM:616494" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 11" />
      </concept>
      <concept>
        <code value="OMIM:616500" />
        <display value="CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3" />
      </concept>
      <concept>
        <code value="OMIM:616501" />
        <display value="CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4" />
      </concept>
      <concept>
        <code value="OMIM:616502" />
        <display value="CONE-ROD DYSTROPHY 21" />
      </concept>
      <concept>
        <code value="OMIM:616503" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:616505" />
        <display value="NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB" />
      </concept>
      <concept>
        <code value="OMIM:616507" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XVII" />
      </concept>
      <concept>
        <code value="OMIM:616509" />
        <display value="CATARACT 44" />
      </concept>
      <concept>
        <code value="OMIM:616511" />
        <display value="MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14" />
      </concept>
      <concept>
        <code value="OMIM:616515" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 104" />
      </concept>
      <concept>
        <code value="OMIM:616516" />
        <display value="EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616517" />
        <display value="ACHROMATOPSIA 7" />
      </concept>
      <concept>
        <code value="OMIM:616521" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 39" />
      </concept>
      <concept>
        <code value="OMIM:616531" />
        <display value="POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS" />
      </concept>
      <concept>
        <code value="OMIM:616532" />
        <display value="ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:616534" />
        <display value="THYROID CANCER, NONMEDULLARY, 4" />
      </concept>
      <concept>
        <code value="OMIM:616535" />
        <display value="THYROID CANCER, NONMEDULLARY, 5" />
      </concept>
      <concept>
        <code value="OMIM:616538" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9" />
      </concept>
      <concept>
        <code value="OMIM:616539" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26" />
      </concept>
      <concept>
        <code value="OMIM:616540" />
        <display value="EPILEPSY, PROGRESSIVE MYOCLONIC, 9" />
      </concept>
      <concept>
        <code value="OMIM:616541" />
        <display value="SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:616544" />
        <display value="RETINITIS PIGMENTOSA 73" />
      </concept>
      <concept>
        <code value="OMIM:616546" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:616549" />
        <display value="KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM" />
      </concept>
      <concept>
        <code value="OMIM:616553" />
        <display value="DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6" />
      </concept>
      <concept>
        <code value="OMIM:616559" />
        <display value="NOONAN SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:616562" />
        <display value="RETINITIS PIGMENTOSA 74" />
      </concept>
      <concept>
        <code value="OMIM:616564" />
        <display value="NOONAN SYNDROME 10" />
      </concept>
      <concept>
        <code value="OMIM:616566" />
        <display value="SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616568" />
        <display value="GLIOMA SUSCEPTIBILITY 9" />
      </concept>
      <concept>
        <code value="OMIM:616570" />
        <display value="CEREBROOCULOFACIOSKELETAL SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:616576" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 12" />
      </concept>
      <concept>
        <code value="OMIM:616577" />
        <display value="EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616579" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 40" />
      </concept>
      <concept>
        <code value="OMIM:616580" />
        <display value="AU-KLINE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616583" />
        <display value="SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE" />
      </concept>
      <concept>
        <code value="OMIM:616586" />
        <display value="SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616589" />
        <display value="ADAMS-OLIVER SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:616592" />
        <display value="KOSAKI OVERGROWTH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616602" />
        <display value="CRANIOSYNOSTOSIS 6" />
      </concept>
      <concept>
        <code value="OMIM:616603" />
        <display value="CUTIS LAXA, AUTOSOMAL DOMINANT 3" />
      </concept>
      <concept>
        <code value="OMIM:616604" />
        <display value="CHROMOSOME 14q32 DUPLICATION SYNDROME, 700-KB" />
      </concept>
      <concept>
        <code value="OMIM:616606" />
        <display value="RING CHROMOSOME 14 SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616617" />
        <display value="HEIMLER SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:616622" />
        <display value="IMMUNODEFICIENCY 42" />
      </concept>
      <concept>
        <code value="OMIM:616625" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W" />
      </concept>
      <concept>
        <code value="OMIM:616629" />
        <display value="SENIOR-LOKEN SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:616631" />
        <display value="POROKERATOSIS 9, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:616632" />
        <display value="SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616636" />
        <display value="IMMUNODEFICIENCY 44" />
      </concept>
      <concept>
        <code value="OMIM:616638" />
        <display value="SMITH-KINGSMORE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616640" />
        <display value="EPILEPSY, PROGRESSIVE MYOCLONIC, 10" />
      </concept>
      <concept>
        <code value="OMIM:616645" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34" />
      </concept>
      <concept>
        <code value="OMIM:616647" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35" />
      </concept>
      <concept>
        <code value="OMIM:616648" />
        <display value="OPTIC ATROPHY 8" />
      </concept>
      <concept>
        <code value="OMIM:616649" />
        <display value="SPHEROCYTOSIS, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:616651" />
        <display value="ROIFMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616652" />
        <display value="YUAN-HAREL-LUPSKI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616654" />
        <display value="JOUBERT SYNDROME 24" />
      </concept>
      <concept>
        <code value="OMIM:616657" />
        <display value="SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY" />
      </concept>
      <concept>
        <code value="OMIM:616668" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X" />
      </concept>
      <concept>
        <code value="OMIM:616669" />
        <display value="IMMUNODEFICIENCY 45" />
      </concept>
      <concept>
        <code value="OMIM:616672" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27" />
      </concept>
      <concept>
        <code value="OMIM:616680" />
        <display value="SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616681" />
        <display value="MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616682" />
        <display value="SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616683" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 12" />
      </concept>
      <concept>
        <code value="OMIM:616684" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K" />
      </concept>
      <concept>
        <code value="OMIM:616685" />
        <display value="EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14" />
      </concept>
      <concept>
        <code value="OMIM:616687" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y" />
      </concept>
      <concept>
        <code value="OMIM:616688" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z" />
      </concept>
      <concept>
        <code value="OMIM:616689" />
        <display value="DEHYDRATED HEREDITARY STOMATOCYTOSIS 2" />
      </concept>
      <concept>
        <code value="OMIM:616697" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 69" />
      </concept>
      <concept>
        <code value="OMIM:616705" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 97" />
      </concept>
      <concept>
        <code value="OMIM:616707" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 68" />
      </concept>
      <concept>
        <code value="OMIM:616708" />
        <display value="DESANTO-SHINAWI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616710" />
        <display value="PARKINSON DISEASE 22, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:616716" />
        <display value="RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:616719" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21" />
      </concept>
      <concept>
        <code value="OMIM:616720" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 19" />
      </concept>
      <concept>
        <code value="OMIM:616721" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn" />
      </concept>
      <concept>
        <code value="OMIM:616722" />
        <display value="RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT" />
      </concept>
      <concept>
        <code value="OMIM:616723" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:616724" />
        <display value="TOOTH AGENESIS, SELECTIVE, 7" />
      </concept>
      <concept>
        <code value="OMIM:616726" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 33" />
      </concept>
      <concept>
        <code value="OMIM:616728" />
        <display value="CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:616730" />
        <display value="NEPHROTIC SYNDROME, TYPE 11" />
      </concept>
      <concept>
        <code value="OMIM:616732" />
        <display value="OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:616733" />
        <display value="COENZYME Q10 DEFICIENCY, PRIMARY, 8" />
      </concept>
      <concept>
        <code value="OMIM:616734" />
        <display value="SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:616736" />
        <display value="TREMOR, HEREDITARY ESSENTIAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:616737" />
        <display value="TAKENOUCHI-KOSAKI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616738" />
        <display value="RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2" />
      </concept>
      <concept>
        <code value="OMIM:616739" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51" />
      </concept>
      <concept>
        <code value="OMIM:616740" />
        <display value="IMMUNODEFICIENCY 46" />
      </concept>
      <concept>
        <code value="OMIM:616744" />
        <display value="AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE" />
      </concept>
      <concept>
        <code value="OMIM:616749" />
        <display value="HETEROTAXY, VISCERAL, 7, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:616754" />
        <display value="BOMBAY PHENOTYPE" />
      </concept>
      <concept>
        <code value="OMIM:616756" />
        <display value="SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:616760" />
        <display value="WOOLLY HAIR, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:616763" />
        <display value="LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA" />
      </concept>
      <concept>
        <code value="OMIM:616777" />
        <display value="SECKEL SYNDROME 9" />
      </concept>
      <concept>
        <code value="OMIM:616779" />
        <display value="CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2" />
      </concept>
      <concept>
        <code value="OMIM:616780" />
        <display value="OOCYTE MATURATION DEFECT 2" />
      </concept>
      <concept>
        <code value="OMIM:616781" />
        <display value="JOUBERT SYNDROME 25" />
      </concept>
      <concept>
        <code value="OMIM:616784" />
        <display value="JOUBERT SYNDROME 26" />
      </concept>
      <concept>
        <code value="OMIM:616788" />
        <display value="OROFACIAL CLEFT 15" />
      </concept>
      <concept>
        <code value="OMIM:616789" />
        <display value="MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:616792" />
        <display value="NEUROBLASTOMA, SUSCEPTIBILITY TO, 7" />
      </concept>
      <concept>
        <code value="OMIM:616794" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28" />
      </concept>
      <concept>
        <code value="OMIM:616795" />
        <display value="SPINOCEREBELLAR ATAXIA 42" />
      </concept>
      <concept>
        <code value="OMIM:616801" />
        <display value="HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2" />
      </concept>
      <concept>
        <code value="OMIM:616803" />
        <display value="LAMB-SHAFFER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616806" />
        <display value="WILMS TUMOR 6" />
      </concept>
      <concept>
        <code value="OMIM:616809" />
        <display value="HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:616811" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29" />
      </concept>
      <concept>
        <code value="OMIM:616812" />
        <display value="CARDIAC ARRHYTHMIA WITH INCREASED SERUM CREATINE KINASE" />
      </concept>
      <concept>
        <code value="OMIM:616814" />
        <display value="PREIMPLANTATION EMBRYONIC LETHALITY 1" />
      </concept>
      <concept>
        <code value="OMIM:616816" />
        <display value="HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:616817" />
        <display value="MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2" />
      </concept>
      <concept>
        <code value="OMIM:616818" />
        <display value="IgA NEPHROPATHY, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:616819" />
        <display value="CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:616827" />
        <display value="MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, WITH CARDIOMYOPATHY AND TRIANGULAR TONGUE" />
      </concept>
      <concept>
        <code value="OMIM:616828" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIo" />
      </concept>
      <concept>
        <code value="OMIM:616829" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp" />
      </concept>
      <concept>
        <code value="OMIM:616831" />
        <display value="LUSCAN-LUMISH SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616833" />
        <display value="PAGET DISEASE OF BONE 6" />
      </concept>
      <concept>
        <code value="OMIM:616834" />
        <display value="MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS" />
      </concept>
      <concept>
        <code value="OMIM:616835" />
        <display value="MEIER-GORLIN SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:616839" />
        <display value="EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616840" />
        <display value="PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:616843" />
        <display value="LYMPHEDEMA, HEREDITARY, III" />
      </concept>
      <concept>
        <code value="OMIM:616849" />
        <display value="BRACHYDACTYLY, TYPE A1, D" />
      </concept>
      <concept>
        <code value="OMIM:616851" />
        <display value="CATARACT 45" />
      </concept>
      <concept>
        <code value="OMIM:616852" />
        <display value="MYOPATHY, SCAPULOHUMEROPERONEAL" />
      </concept>
      <concept>
        <code value="OMIM:616854" />
        <display value="EVEN-PLUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616858" />
        <display value="COWDEN SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:616859" />
        <display value="SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:616860" />
        <display value="ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY" />
      </concept>
      <concept>
        <code value="OMIM:616863" />
        <display value="CHROMOSOME 16p13.2 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616866" />
        <display value="SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1" />
      </concept>
      <concept>
        <code value="OMIM:616867" />
        <display value="SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2" />
      </concept>
      <concept>
        <code value="OMIM:616868" />
        <display value="DIARRHEA 8, SECRETORY SODIUM, CONGENITAL" />
      </concept>
      <concept>
        <code value="OMIM:616871" />
        <display value="MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:616873" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 13" />
      </concept>
      <concept>
        <code value="OMIM:616875" />
        <display value="CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:616878" />
        <display value="METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION" />
      </concept>
      <concept>
        <code value="OMIM:616881" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 13" />
      </concept>
      <concept>
        <code value="OMIM:616882" />
        <display value="ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:616887" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52" />
      </concept>
      <concept>
        <code value="OMIM:616890" />
        <display value="SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:616892" />
        <display value="NEPHROTIC SYNDROME, TYPE 12" />
      </concept>
      <concept>
        <code value="OMIM:616893" />
        <display value="NEPHROTIC SYNDROME, TYPE 13" />
      </concept>
      <concept>
        <code value="OMIM:616894" />
        <display value="ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3" />
      </concept>
      <concept>
        <code value="OMIM:616896" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:616897" />
        <display value="OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE" />
      </concept>
      <concept>
        <code value="OMIM:616898" />
        <display value="CHROMOSOME 15q14 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616900" />
        <display value="HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3" />
      </concept>
      <concept>
        <code value="OMIM:616901" />
        <display value="DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR" />
      </concept>
      <concept>
        <code value="OMIM:616902" />
        <display value="CHROMOSOME 11p13 DELETION SYNDROME, DISTAL" />
      </concept>
      <concept>
        <code value="OMIM:616903" />
        <display value="THIOPURINES, POOR METABOLISM OF, 2" />
      </concept>
      <concept>
        <code value="OMIM:616907" />
        <display value="SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:616910" />
        <display value="IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:616911" />
        <display value="IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:616913" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 20" />
      </concept>
      <concept>
        <code value="OMIM:616914" />
        <display value="MARFAN LIPODYSTROPHY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616917" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53" />
      </concept>
      <concept>
        <code value="OMIM:616920" />
        <display value="HEART AND BRAIN MALFORMATION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616921" />
        <display value="DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:616922" />
        <display value="STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2" />
      </concept>
      <concept>
        <code value="OMIM:616924" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC" />
      </concept>
      <concept>
        <code value="OMIM:616937" />
        <display value="THROMBOCYTOPENIA 6" />
      </concept>
      <concept>
        <code value="OMIM:616938" />
        <display value="COFFIN-SIRIS SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:616939" />
        <display value="CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:616941" />
        <display value="AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:616943" />
        <display value="TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE" />
      </concept>
      <concept>
        <code value="OMIM:616944" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 41" />
      </concept>
      <concept>
        <code value="OMIM:616946" />
        <display value="PREMATURE OVARIAN FAILURE 11" />
      </concept>
      <concept>
        <code value="OMIM:616947" />
        <display value="PREMATURE OVARIAN FAILURE 12" />
      </concept>
      <concept>
        <code value="OMIM:616948" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22" />
      </concept>
      <concept>
        <code value="OMIM:616949" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23" />
      </concept>
      <concept>
        <code value="OMIM:616950" />
        <display value="SPERMATOGENIC FAILURE 15" />
      </concept>
      <concept>
        <code value="OMIM:616954" />
        <display value="YOU-HOOVER-FONG SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:616959" />
        <display value="RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:616963" />
        <display value="HYPERCALCEMIA, INFANTILE, 2" />
      </concept>
      <concept>
        <code value="OMIM:616968" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 70" />
      </concept>
      <concept>
        <code value="OMIM:616969" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 66" />
      </concept>
      <concept>
        <code value="OMIM:616973" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 42" />
      </concept>
      <concept>
        <code value="OMIM:616974" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30" />
      </concept>
      <concept>
        <code value="OMIM:616975" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART" />
      </concept>
      <concept>
        <code value="OMIM:616977" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 43" />
      </concept>
      <concept>
        <code value="OMIM:616981" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37" />
      </concept>
      <concept>
        <code value="OMIM:617004" />
        <display value="POLYCYSTIC LIVER DISEASE 2 WITH OR WITHOUT KIDNEY CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:617006" />
        <display value="AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2" />
      </concept>
      <concept>
        <code value="OMIM:617008" />
        <display value="CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3" />
      </concept>
      <concept>
        <code value="OMIM:617011" />
        <display value="MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION" />
      </concept>
      <concept>
        <code value="OMIM:617013" />
        <display value="HYPERMANGANESEMIA WITH DYSTONIA 2" />
      </concept>
      <concept>
        <code value="OMIM:617014" />
        <display value="NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617017" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T" />
      </concept>
      <concept>
        <code value="OMIM:617018" />
        <display value="SPINOCEREBELLAR ATAXIA 43" />
      </concept>
      <concept>
        <code value="OMIM:617020" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38" />
      </concept>
      <concept>
        <code value="OMIM:617021" />
        <display value="HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA" />
      </concept>
      <concept>
        <code value="OMIM:617022" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 10" />
      </concept>
      <concept>
        <code value="OMIM:617023" />
        <display value="RETINITIS PIGMENTOSA 75" />
      </concept>
      <concept>
        <code value="OMIM:617024" />
        <display value="NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H" />
      </concept>
      <concept>
        <code value="OMIM:617025" />
        <display value="NEVUS COMEDONICUS" />
      </concept>
      <concept>
        <code value="OMIM:617026" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 2F" />
      </concept>
      <concept>
        <code value="OMIM:617027" />
        <display value="HYPERALDOSTERONISM, FAMILIAL, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:617028" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54" />
      </concept>
      <concept>
        <code value="OMIM:617030" />
        <display value="MYOPATHY, DISTAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:617035" />
        <display value="PATENT DUCTUS ARTERIOSUS 2" />
      </concept>
      <concept>
        <code value="OMIM:617039" />
        <display value="PATENT DUCTUS ARTERIOSUS 3" />
      </concept>
      <concept>
        <code value="OMIM:617041" />
        <display value="DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:617044" />
        <display value="SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS" />
      </concept>
      <concept>
        <code value="OMIM:617046" />
        <display value="SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617047" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26" />
      </concept>
      <concept>
        <code value="OMIM:617049" />
        <display value="CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5" />
      </concept>
      <concept>
        <code value="OMIM:617050" />
        <display value="HERMANSKY-PUDLAK SYNDROME 10" />
      </concept>
      <concept>
        <code value="OMIM:617051" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55" />
      </concept>
      <concept>
        <code value="OMIM:617052" />
        <display value="BONE MARROW FAILURE SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:617053" />
        <display value="MIRAGE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617054" />
        <display value="STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:617055" />
        <display value="CRISPONI/COLD-INDUCED SWEATING SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:617056" />
        <display value="HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4" />
      </concept>
      <concept>
        <code value="OMIM:617061" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 44" />
      </concept>
      <concept>
        <code value="OMIM:617062" />
        <display value="OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617063" />
        <display value="MEIER-GORLIN SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:617065" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40" />
      </concept>
      <concept>
        <code value="OMIM:617066" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE" />
      </concept>
      <concept>
        <code value="OMIM:617068" />
        <display value="PORTAL HYPERTENSION, NONCIRRHOTIC" />
      </concept>
      <concept>
        <code value="OMIM:617069" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3" />
      </concept>
      <concept>
        <code value="OMIM:617070" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4" />
      </concept>
      <concept>
        <code value="OMIM:617072" />
        <display value="MYOPATHY, AUTOSOMAL RECESSIVE, WITH RIGID SPINE AND DISTAL JOINT CONTRACTURES" />
      </concept>
      <concept>
        <code value="OMIM:617073" />
        <display value="TOOTH AGENESIS, SELECTIVE, 8" />
      </concept>
      <concept>
        <code value="OMIM:617075" />
        <display value="NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 3" />
      </concept>
      <concept>
        <code value="OMIM:617080" />
        <display value="SEIZURES, BENIGN FAMILIAL INFANTILE, 5" />
      </concept>
      <concept>
        <code value="OMIM:617082" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa" />
      </concept>
      <concept>
        <code value="OMIM:617086" />
        <display value="ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2" />
      </concept>
      <concept>
        <code value="OMIM:617087" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B" />
      </concept>
      <concept>
        <code value="OMIM:617088" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:617090" />
        <display value="MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617091" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 34" />
      </concept>
      <concept>
        <code value="OMIM:617092" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 35" />
      </concept>
      <concept>
        <code value="OMIM:617093" />
        <display value="GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:617099" />
        <display value="AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617100" />
        <display value="FAMILIAL ADENOMATOUS POLYPOSIS 4" />
      </concept>
      <concept>
        <code value="OMIM:617101" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN" />
      </concept>
      <concept>
        <code value="OMIM:617102" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:617105" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41" />
      </concept>
      <concept>
        <code value="OMIM:617106" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42" />
      </concept>
      <concept>
        <code value="OMIM:617107" />
        <display value="THAUVIN-ROBINET-FAIVRE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617108" />
        <display value="SESSILE SERRATED POLYPOSIS CANCER SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617111" />
        <display value="MACULAR DYSTROPHY, PATTERNED, 3" />
      </concept>
      <concept>
        <code value="OMIM:617113" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43" />
      </concept>
      <concept>
        <code value="OMIM:617114" />
        <display value="MYOPATHY, MYOFIBRILLAR, 7" />
      </concept>
      <concept>
        <code value="OMIM:617115" />
        <display value="PEELING SKIN SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:617116" />
        <display value="EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2" />
      </concept>
      <concept>
        <code value="OMIM:617118" />
        <display value="EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3" />
      </concept>
      <concept>
        <code value="OMIM:617119" />
        <display value="BARDET-BIEDL SYNDROME 20" />
      </concept>
      <concept>
        <code value="OMIM:617120" />
        <display value="JOUBERT SYNDROME 27" />
      </concept>
      <concept>
        <code value="OMIM:617121" />
        <display value="JOUBERT SYNDROME 28" />
      </concept>
      <concept>
        <code value="OMIM:617123" />
        <display value="RETINITIS PIGMENTOSA 76" />
      </concept>
      <concept>
        <code value="OMIM:617125" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 56" />
      </concept>
      <concept>
        <code value="OMIM:617126" />
        <display value="ALAZAMI-YUAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617127" />
        <display value="OROFACIODIGITAL SYNDROME XV" />
      </concept>
      <concept>
        <code value="OMIM:617132" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44" />
      </concept>
      <concept>
        <code value="OMIM:617133" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24" />
      </concept>
      <concept>
        <code value="OMIM:617137" />
        <display value="FRONTOMETAPHYSEAL DYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:617140" />
        <display value="ZTTK SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617141" />
        <display value="ANIRIDIA 2" />
      </concept>
      <concept>
        <code value="OMIM:617142" />
        <display value="ANIRIDIA 3" />
      </concept>
      <concept>
        <code value="OMIM:617143" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC" />
      </concept>
      <concept>
        <code value="OMIM:617145" />
        <display value="NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:617146" />
        <display value="ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH" />
      </concept>
      <concept>
        <code value="OMIM:617153" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45" />
      </concept>
      <concept>
        <code value="OMIM:617156" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE)" />
      </concept>
      <concept>
        <code value="OMIM:617157" />
        <display value="SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:617158" />
        <display value="MYOPATHY, DISTAL, WITH RIMMED VACUOLES" />
      </concept>
      <concept>
        <code value="OMIM:617159" />
        <display value="SIFRIM-HITZ-WEISS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617162" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46" />
      </concept>
      <concept>
        <code value="OMIM:617164" />
        <display value="SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:617166" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47" />
      </concept>
      <concept>
        <code value="OMIM:617168" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 10" />
      </concept>
      <concept>
        <code value="OMIM:617169" />
        <display value="SOTOS SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:617171" />
        <display value="DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:617173" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA" />
      </concept>
      <concept>
        <code value="OMIM:617174" />
        <display value="EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2" />
      </concept>
      <concept>
        <code value="OMIM:617175" />
        <display value="RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:617180" />
        <display value="CHITAYAT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617182" />
        <display value="LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA" />
      </concept>
      <concept>
        <code value="OMIM:617183" />
        <display value="HAREL-YOON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617184" />
        <display value="MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:617186" />
        <display value="ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY" />
      </concept>
      <concept>
        <code value="OMIM:617187" />
        <display value="SPERMATOGENIC FAILURE 16" />
      </concept>
      <concept>
        <code value="OMIM:617188" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57" />
      </concept>
      <concept>
        <code value="OMIM:617190" />
        <display value="SHASHI-PENA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617193" />
        <display value="ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM" />
      </concept>
      <concept>
        <code value="OMIM:617194" />
        <display value="LETHAL CONGENITAL CONTRACTURE SYNDROME 11" />
      </concept>
      <concept>
        <code value="OMIM:617201" />
        <display value="PERIVENTRICULAR NODULAR HETEROTOPIA 7" />
      </concept>
      <concept>
        <code value="OMIM:617205" />
        <display value="HETEROTAXY, VISCERAL, 8, AUTOSOMAL" />
      </concept>
      <concept>
        <code value="OMIM:617207" />
        <display value="ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:617213" />
        <display value="SEDOHEPTULOKINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:617214" />
        <display value="SPERMATOGENIC FAILURE 17" />
      </concept>
      <concept>
        <code value="OMIM:617217" />
        <display value="AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6" />
      </concept>
      <concept>
        <code value="OMIM:617219" />
        <display value="CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL" />
      </concept>
      <concept>
        <code value="OMIM:617222" />
        <display value="SUDDEN CARDIAC FAILURE, INFANTILE" />
      </concept>
      <concept>
        <code value="OMIM:617223" />
        <display value="SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED" />
      </concept>
      <concept>
        <code value="OMIM:617225" />
        <display value="SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617228" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31" />
      </concept>
      <concept>
        <code value="OMIM:617232" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 21" />
      </concept>
      <concept>
        <code value="OMIM:617234" />
        <display value="PREIMPLANTATION EMBRYONIC LETHALITY 2" />
      </concept>
      <concept>
        <code value="OMIM:617235" />
        <display value="MYOCLONUS, INTRACTABLE, NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:617236" />
        <display value="CONE-ROD DYSTROPHY AND HEARING LOSS" />
      </concept>
      <concept>
        <code value="OMIM:617237" />
        <display value="IMMUNODEFICIENCY 49" />
      </concept>
      <concept>
        <code value="OMIM:617238" />
        <display value="MYOPIA 25, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:617239" />
        <display value="MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC" />
      </concept>
      <concept>
        <code value="OMIM:617241" />
        <display value="LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617243" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP V" />
      </concept>
      <concept>
        <code value="OMIM:617244" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP R" />
      </concept>
      <concept>
        <code value="OMIM:617247" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP U" />
      </concept>
      <concept>
        <code value="OMIM:617248" />
        <display value="3-METHYLGLUTACONIC ACIDURIA, TYPE VIII" />
      </concept>
      <concept>
        <code value="OMIM:617251" />
        <display value="UNCOMBABLE HAIR SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:617252" />
        <display value="UNCOMBABLE HAIR SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:617253" />
        <display value="SECKEL SYNDROME 10" />
      </concept>
      <concept>
        <code value="OMIM:617255" />
        <display value="LISSENCEPHALY 8" />
      </concept>
      <concept>
        <code value="OMIM:617258" />
        <display value="MYOPATHY, MYOFIBRILLAR, 8" />
      </concept>
      <concept>
        <code value="OMIM:617260" />
        <display value="GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES" />
      </concept>
      <concept>
        <code value="OMIM:617268" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE" />
      </concept>
      <concept>
        <code value="OMIM:617270" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58" />
      </concept>
      <concept>
        <code value="OMIM:617271" />
        <display value="NEPHRONOPHTHISIS 20" />
      </concept>
      <concept>
        <code value="OMIM:617272" />
        <display value="GLAUCOMA 3, PRIMARY CONGENITAL, E" />
      </concept>
      <concept>
        <code value="OMIM:617275" />
        <display value="TOOTH AGENESIS, SELECTIVE, 9" />
      </concept>
      <concept>
        <code value="OMIM:617276" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48" />
      </concept>
      <concept>
        <code value="OMIM:617280" />
        <display value="ATRIAL FIBRILLATION, FAMILIAL, 18" />
      </concept>
      <concept>
        <code value="OMIM:617281" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49" />
      </concept>
      <concept>
        <code value="OMIM:617282" />
        <display value="DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:617284" />
        <display value="DYSTONIA 28, CHILDHOOD-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:617290" />
        <display value="EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT" />
      </concept>
      <concept>
        <code value="OMIM:617294" />
        <display value="EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS" />
      </concept>
      <concept>
        <code value="OMIM:617296" />
        <display value="SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY" />
      </concept>
      <concept>
        <code value="OMIM:617297" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IJ" />
      </concept>
      <concept>
        <code value="OMIM:617300" />
        <display value="HYDROPS FETALIS, NONIMMUNE, AND/OR ATRIAL SEPTAL DEFECT, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:617301" />
        <display value="GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE" />
      </concept>
      <concept>
        <code value="OMIM:617302" />
        <display value="OPTIC ATROPHY 11" />
      </concept>
      <concept>
        <code value="OMIM:617303" />
        <display value="MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617304" />
        <display value="RETINITIS PIGMENTOSA 77" />
      </concept>
      <concept>
        <code value="OMIM:617306" />
        <display value="COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:617308" />
        <display value="BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:617315" />
        <display value="ANTERIOR SEGMENT DYSGENESIS 6" />
      </concept>
      <concept>
        <code value="OMIM:617319" />
        <display value="ANTERIOR SEGMENT DYSGENESIS 8" />
      </concept>
      <concept>
        <code value="OMIM:617320" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12" />
      </concept>
      <concept>
        <code value="OMIM:617321" />
        <display value="YAO SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617323" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59" />
      </concept>
      <concept>
        <code value="OMIM:617330" />
        <display value="HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617333" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS" />
      </concept>
      <concept>
        <code value="OMIM:617336" />
        <display value="NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617337" />
        <display value="ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE" />
      </concept>
      <concept>
        <code value="OMIM:617339" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51" />
      </concept>
      <concept>
        <code value="OMIM:617341" />
        <display value="CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2" />
      </concept>
      <concept>
        <code value="OMIM:617343" />
        <display value="HYPERPARATHYROIDISM 4" />
      </concept>
      <concept>
        <code value="OMIM:617347" />
        <display value="HYPERLIPOPROTEINEMIA, TYPE III" />
      </concept>
      <concept>
        <code value="OMIM:617349" />
        <display value="AORTIC ANEURYSM, FAMILIAL THORACIC 11, SUSCEPTIBILITY TO" />
      </concept>
      <concept>
        <code value="OMIM:617350" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52" />
      </concept>
      <concept>
        <code value="OMIM:617352" />
        <display value="MULCHANDANI-BHOJ-CONLIN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617360" />
        <display value="CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER" />
      </concept>
      <concept>
        <code value="OMIM:617364" />
        <display value="CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA" />
      </concept>
      <concept>
        <code value="OMIM:617370" />
        <display value="PEROXISOME BIOGENESIS DISORDER 10B" />
      </concept>
      <concept>
        <code value="OMIM:617383" />
        <display value="AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2" />
      </concept>
      <concept>
        <code value="OMIM:617384" />
        <display value="HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT" />
      </concept>
      <concept>
        <code value="OMIM:617386" />
        <display value="NUCLEAR RECEPTOR SUBFAMILY 1, GROUP H, MEMBER 5, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:617388" />
        <display value="AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS" />
      </concept>
      <concept>
        <code value="OMIM:617389" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53" />
      </concept>
      <concept>
        <code value="OMIM:617391" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54" />
      </concept>
      <concept>
        <code value="OMIM:617392" />
        <display value="ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE" />
      </concept>
      <concept>
        <code value="OMIM:617393" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION" />
      </concept>
      <concept>
        <code value="OMIM:617394" />
        <display value="SCLEROSING CHOLANGITIS, NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:617395" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq" />
      </concept>
      <concept>
        <code value="OMIM:617396" />
        <display value="ANAUXETIC DYSPLASIA 2" />
      </concept>
      <concept>
        <code value="OMIM:617397" />
        <display value="PSEUDO-TORCH SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:617402" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC" />
      </concept>
      <concept>
        <code value="OMIM:617403" />
        <display value="CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID" />
      </concept>
      <concept>
        <code value="OMIM:617404" />
        <display value="MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY" />
      </concept>
      <concept>
        <code value="OMIM:617405" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:617406" />
        <display value="BARDET-BIEDL SYNDROME 21" />
      </concept>
      <concept>
        <code value="OMIM:617408" />
        <display value="DIAMOND-BLACKFAN ANEMIA 16" />
      </concept>
      <concept>
        <code value="OMIM:617409" />
        <display value="DIAMOND-BLACKFAN ANEMIA 17" />
      </concept>
      <concept>
        <code value="OMIM:617412" />
        <display value="BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:617425" />
        <display value="IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:617432" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60" />
      </concept>
      <concept>
        <code value="OMIM:617433" />
        <display value="RETINITIS PIGMENTOSA 78" />
      </concept>
      <concept>
        <code value="OMIM:617435" />
        <display value="LOPES-MACIEL-RODAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617439" />
        <display value="CRANIOSYNOSTOSIS 7" />
      </concept>
      <concept>
        <code value="OMIM:617441" />
        <display value="THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS" />
      </concept>
      <concept>
        <code value="OMIM:617442" />
        <display value="PREMATURE OVARIAN FAILURE 13" />
      </concept>
      <concept>
        <code value="OMIM:617443" />
        <display value="BLEEDING DISORDER, PLATELET-TYPE, 21" />
      </concept>
      <concept>
        <code value="OMIM:617450" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD" />
      </concept>
      <concept>
        <code value="OMIM:617452" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:617460" />
        <display value="RETINITIS PIGMENTOSA 79" />
      </concept>
      <concept>
        <code value="OMIM:617466" />
        <display value="TOWNES-BROCKS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:617468" />
        <display value="ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT" />
      </concept>
      <concept>
        <code value="OMIM:617475" />
        <display value="SPECIFIC GRANULE DEFICIENCY 2" />
      </concept>
      <concept>
        <code value="OMIM:617478" />
        <display value="STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617480" />
        <display value="46,XX SEX REVERSAL 4" />
      </concept>
      <concept>
        <code value="OMIM:617481" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:617493" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS" />
      </concept>
      <concept>
        <code value="OMIM:617506" />
        <display value="NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2" />
      </concept>
      <concept>
        <code value="OMIM:617507" />
        <display value="PEHO-LIKE SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617514" />
        <display value="IMMUNODEFICIENCY 52" />
      </concept>
      <concept>
        <code value="OMIM:617516" />
        <display value="STANKIEWICZ-ISIDOR SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617519" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:617520" />
        <display value="MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT" />
      </concept>
      <concept>
        <code value="OMIM:617523" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS" />
      </concept>
      <concept>
        <code value="OMIM:617524" />
        <display value="ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2" />
      </concept>
      <concept>
        <code value="OMIM:617525" />
        <display value="ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3" />
      </concept>
      <concept>
        <code value="OMIM:617526" />
        <display value="ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4" />
      </concept>
      <concept>
        <code value="OMIM:617527" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:617532" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:617537" />
        <display value="RAHMAN SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617540" />
        <display value="PITUITARY ADENOMA 5, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:617542" />
        <display value="GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2" />
      </concept>
      <concept>
        <code value="OMIM:617547" />
        <display value="RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA" />
      </concept>
      <concept>
        <code value="OMIM:617557" />
        <display value="GABRIELE-DE VRIES SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617560" />
        <display value="SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY" />
      </concept>
      <concept>
        <code value="OMIM:617561" />
        <display value="COHEN-GIBSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617562" />
        <display value="MECKEL SYNDROME 13" />
      </concept>
      <concept>
        <code value="OMIM:617563" />
        <display value="OROFACIODIGITAL SYNDROME XVI" />
      </concept>
      <concept>
        <code value="OMIM:617564" />
        <display value="MEIER-GORLIN SYNDROME 8" />
      </concept>
      <concept>
        <code value="OMIM:617565" />
        <display value="PERRAULT SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:617571" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14" />
      </concept>
      <concept>
        <code value="OMIM:617572" />
        <display value="EXUDATIVE VITREORETINOPATHY 7" />
      </concept>
      <concept>
        <code value="OMIM:617574" />
        <display value="ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 13" />
      </concept>
      <concept>
        <code value="OMIM:617575" />
        <display value="NEPHROTIC SYNDROME, TYPE 14" />
      </concept>
      <concept>
        <code value="OMIM:617576" />
        <display value="SPERMATOGENIC FAILURE 18" />
      </concept>
      <concept>
        <code value="OMIM:617577" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 37" />
      </concept>
      <concept>
        <code value="OMIM:617584" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25" />
      </concept>
      <concept>
        <code value="OMIM:617585" />
        <display value="IMMUNODEFICIENCY 53" />
      </concept>
      <concept>
        <code value="OMIM:617591" />
        <display value="PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:617592" />
        <display value="SPERMATOGENIC FAILURE 19" />
      </concept>
      <concept>
        <code value="OMIM:617593" />
        <display value="SPERMATOGENIC FAILURE 20" />
      </concept>
      <concept>
        <code value="OMIM:617595" />
        <display value="BIRK-LANDAU-PEREZ SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617596" />
        <display value="MALEYLACETOACETATE ISOMERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:617598" />
        <display value="MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:617599" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55" />
      </concept>
      <concept>
        <code value="OMIM:617600" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 45" />
      </concept>
      <concept>
        <code value="OMIM:617601" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 46" />
      </concept>
      <concept>
        <code value="OMIM:617602" />
        <display value="CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617604" />
        <display value="MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:617605" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 71" />
      </concept>
      <concept>
        <code value="OMIM:617606" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 72" />
      </concept>
      <concept>
        <code value="OMIM:617607" />
        <display value="AMELOGENESIS IMPERFECTA, TYPE IIIB" />
      </concept>
      <concept>
        <code value="OMIM:617609" />
        <display value="NEPHROTIC SYNDROME, TYPE 15" />
      </concept>
      <concept>
        <code value="OMIM:617610" />
        <display value="POLYCYSTIC KIDNEY DISEASE 5" />
      </concept>
      <concept>
        <code value="OMIM:617613" />
        <display value="MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:617616" />
        <display value="SKRABAN-DEARDORFF SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617622" />
        <display value="JOUBERT SYNDROME 30" />
      </concept>
      <concept>
        <code value="OMIM:617626" />
        <display value="FIBROMATOSIS, GINGIVAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:617629" />
        <display value="SCHIZOPHRENIA 19" />
      </concept>
      <concept>
        <code value="OMIM:617633" />
        <display value="SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26" />
      </concept>
      <concept>
        <code value="OMIM:617635" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 47" />
      </concept>
      <concept>
        <code value="OMIM:617637" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 106" />
      </concept>
      <concept>
        <code value="OMIM:617638" />
        <display value="IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS" />
      </concept>
      <concept>
        <code value="OMIM:617639" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 107" />
      </concept>
      <concept>
        <code value="OMIM:617641" />
        <display value="CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:617642" />
        <display value="POLYDACTYLY, POSTAXIAL, TYPE A7" />
      </concept>
      <concept>
        <code value="OMIM:617643" />
        <display value="CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:617644" />
        <display value="SPERMATOGENIC FAILURE 21" />
      </concept>
      <concept>
        <code value="OMIM:617654" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 108" />
      </concept>
      <concept>
        <code value="OMIM:617660" />
        <display value="VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1" />
      </concept>
      <concept>
        <code value="OMIM:617661" />
        <display value="VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:617662" />
        <display value="JOINT LAXITY, SHORT STATURE, AND MYOPIA" />
      </concept>
      <concept>
        <code value="OMIM:617663" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 73" />
      </concept>
      <concept>
        <code value="OMIM:617664" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32" />
      </concept>
      <concept>
        <code value="OMIM:617665" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56" />
      </concept>
      <concept>
        <code value="OMIM:617666" />
        <display value="FRASER SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:617667" />
        <display value="FRASER SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:617668" />
        <display value="ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:617669" />
        <display value="ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY" />
      </concept>
      <concept>
        <code value="OMIM:617671" />
        <display value="HELIX SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617672" />
        <display value="NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:617675" />
        <display value="MYOPATHY, MITOCHONDRIAL, AND ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:617681" />
        <display value="BLEPHAROCHEILODONTIC SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:617682" />
        <display value="PILAROWSKI-BJORNSSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617686" />
        <display value="PITUITARY ADENOMA 3, MULTIPLE TYPES" />
      </concept>
      <concept>
        <code value="OMIM:617690" />
        <display value="OVARIAN DYSGENESIS 5" />
      </concept>
      <concept>
        <code value="OMIM:617691" />
        <display value="SPINOCEREBELLAR ATAXIA 44" />
      </concept>
      <concept>
        <code value="OMIM:617694" />
        <display value="AL KAISSI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617695" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 11" />
      </concept>
      <concept>
        <code value="OMIM:617698" />
        <display value="3-METHYLGLUTACONIC ACIDURIA, TYPE IX" />
      </concept>
      <concept>
        <code value="OMIM:617706" />
        <display value="SPERMATOGENIC FAILURE 22" />
      </concept>
      <concept>
        <code value="OMIM:617707" />
        <display value="SPERMATOGENIC FAILURE 23" />
      </concept>
      <concept>
        <code value="OMIM:617709" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:617710" />
        <display value="NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:617711" />
        <display value="EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1" />
      </concept>
      <concept>
        <code value="OMIM:617712" />
        <display value="OOCYTE MATURATION DEFECT 3" />
      </concept>
      <concept>
        <code value="OMIM:617713" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33" />
      </concept>
      <concept>
        <code value="OMIM:617717" />
        <display value="AUDITORY NEUROPATHY AND OPTIC ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:617718" />
        <display value="PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:617719" />
        <display value="EPIPHYSEAL DYSPLASIA, MULTIPLE, 7" />
      </concept>
      <concept>
        <code value="OMIM:617721" />
        <display value="NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IX" />
      </concept>
      <concept>
        <code value="OMIM:617729" />
        <display value="GALLOWAY-MOWAT SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:617730" />
        <display value="GALLOWAY-MOWAT SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:617731" />
        <display value="GALLOWAY-MOWAT SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:617732" />
        <display value="FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION" />
      </concept>
      <concept>
        <code value="OMIM:617743" />
        <display value="OOCYTE MATURATION DEFECT 4" />
      </concept>
      <concept>
        <code value="OMIM:617744" />
        <display value="IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:617746" />
        <display value="SWEENEY-COX SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617749" />
        <display value="ACTN3 DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:617751" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 48" />
      </concept>
      <concept>
        <code value="OMIM:617752" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 49" />
      </concept>
      <concept>
        <code value="OMIM:617755" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:617756" />
        <display value="ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 5" />
      </concept>
      <concept>
        <code value="OMIM:617757" />
        <display value="JOUBERT SYNDROME 32" />
      </concept>
      <concept>
        <code value="OMIM:617760" />
        <display value="MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION" />
      </concept>
      <concept>
        <code value="OMIM:617761" />
        <display value="JOUBERT SYNDROME 31" />
      </concept>
      <concept>
        <code value="OMIM:617762" />
        <display value="LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET" />
      </concept>
      <concept>
        <code value="OMIM:617763" />
        <display value="SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES" />
      </concept>
      <concept>
        <code value="OMIM:617765" />
        <display value="IMMUNODEFICIENCY, COMMON VARIABLE, 14" />
      </concept>
      <concept>
        <code value="OMIM:617767" />
        <display value="JOUBERT SYNDROME 33" />
      </concept>
      <concept>
        <code value="OMIM:617768" />
        <display value="KLEEFSTRA SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:617769" />
        <display value="SPINOCEREBELLAR ATAXIA 45" />
      </concept>
      <concept>
        <code value="OMIM:617770" />
        <display value="SPINOCEREBELLAR ATAXIA 46" />
      </concept>
      <concept>
        <code value="OMIM:617771" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57" />
      </concept>
      <concept>
        <code value="OMIM:617772" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION" />
      </concept>
      <concept>
        <code value="OMIM:617773" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61" />
      </concept>
      <concept>
        <code value="OMIM:617780" />
        <display value="COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:617781" />
        <display value="RETINITIS PIGMENTOSA 80" />
      </concept>
      <concept>
        <code value="OMIM:617783" />
        <display value="NEPHROTIC SYNDROME, TYPE 16" />
      </concept>
      <concept>
        <code value="OMIM:617784" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP W" />
      </concept>
      <concept>
        <code value="OMIM:617787" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 50" />
      </concept>
      <concept>
        <code value="OMIM:617788" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 51" />
      </concept>
      <concept>
        <code value="OMIM:617796" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 52" />
      </concept>
      <concept>
        <code value="OMIM:617798" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 53" />
      </concept>
      <concept>
        <code value="OMIM:617799" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 54" />
      </concept>
      <concept>
        <code value="OMIM:617800" />
        <display value="MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617802" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:617804" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE" />
      </concept>
      <concept>
        <code value="OMIM:617805" />
        <display value="RENAL HYPODYSPLASIA/APLASIA 3" />
      </concept>
      <concept>
        <code value="OMIM:617807" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER" />
      </concept>
      <concept>
        <code value="OMIM:617808" />
        <display value="COFFIN-SIRIS SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:617809" />
        <display value="GELEOPHYSIC DYSPLASIA 3" />
      </concept>
      <concept>
        <code value="OMIM:617810" />
        <display value="GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15" />
      </concept>
      <concept>
        <code value="OMIM:617816" />
        <display value="GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16" />
      </concept>
      <concept>
        <code value="OMIM:617820" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617821" />
        <display value="EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2" />
      </concept>
      <concept>
        <code value="OMIM:617822" />
        <display value="ALKURAYA-KUCINSKAS SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617825" />
        <display value="GLUCOCORTICOID DEFICIENCY 5" />
      </concept>
      <concept>
        <code value="OMIM:617827" />
        <display value="IMMUNODEFICIENCY 55" />
      </concept>
      <concept>
        <code value="OMIM:617829" />
        <display value="EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2" />
      </concept>
      <concept>
        <code value="OMIM:617830" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58" />
      </concept>
      <concept>
        <code value="OMIM:617831" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:617836" />
        <display value="DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:617839" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS 23" />
      </concept>
      <concept>
        <code value="OMIM:617854" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 56" />
      </concept>
      <concept>
        <code value="OMIM:617862" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY" />
      </concept>
      <concept>
        <code value="OMIM:617864" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:617865" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:617866" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:617871" />
        <display value="RETINITIS PIGMENTOSA 81" />
      </concept>
      <concept>
        <code value="OMIM:617872" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34" />
      </concept>
      <concept>
        <code value="OMIM:617873" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35" />
      </concept>
      <concept>
        <code value="OMIM:617874" />
        <display value="POLYCYSTIC LIVER DISEASE 3 WITH OR WITHOUT KIDNEY CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:617875" />
        <display value="POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS" />
      </concept>
      <concept>
        <code value="OMIM:617877" />
        <display value="SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:617879" />
        <display value="LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS" />
      </concept>
      <concept>
        <code value="OMIM:617882" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G" />
      </concept>
      <concept>
        <code value="OMIM:617883" />
        <display value="FANCONI ANEMIA, COMPLEMENTATION GROUP S" />
      </concept>
      <concept>
        <code value="OMIM:617885" />
        <display value="BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19" />
      </concept>
      <concept>
        <code value="OMIM:617892" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24" />
      </concept>
      <concept>
        <code value="OMIM:617895" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:617898" />
        <display value="MULTIPLE SYNOSTOSES SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:617899" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 14" />
      </concept>
      <concept>
        <code value="OMIM:617900" />
        <display value="ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8" />
      </concept>
      <concept>
        <code value="OMIM:617903" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS" />
      </concept>
      <concept>
        <code value="OMIM:617904" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59" />
      </concept>
      <concept>
        <code value="OMIM:617907" />
        <display value="ERYTHROCYTOSIS, FAMILIAL, 5" />
      </concept>
      <concept>
        <code value="OMIM:617911" />
        <display value="DIAMOND-BLACKFAN ANEMIA-LIKE" />
      </concept>
      <concept>
        <code value="OMIM:617912" />
        <display value="CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5" />
      </concept>
      <concept>
        <code value="OMIM:617913" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:617914" />
        <display value="MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617915" />
        <display value="HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617916" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7" />
      </concept>
      <concept>
        <code value="OMIM:617917" />
        <display value="NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8" />
      </concept>
      <concept>
        <code value="OMIM:617920" />
        <display value="AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3" />
      </concept>
      <concept>
        <code value="OMIM:617921" />
        <display value="AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 25" />
      </concept>
      <concept>
        <code value="OMIM:617924" />
        <display value="EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10" />
      </concept>
      <concept>
        <code value="OMIM:617925" />
        <display value="SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY" />
      </concept>
      <concept>
        <code value="OMIM:617926" />
        <display value="OROFACIODIGITAL SYNDROME XVII" />
      </concept>
      <concept>
        <code value="OMIM:617927" />
        <display value="OROFACIODIGITAL SYNDROME XVIII" />
      </concept>
      <concept>
        <code value="OMIM:617928" />
        <display value="KERATOCONUS 9" />
      </concept>
      <concept>
        <code value="OMIM:617929" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 60" />
      </concept>
      <concept>
        <code value="OMIM:617930" />
        <display value="CHROMOSOME 1p35 DELETION SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617931" />
        <display value="SPINOCEREBELLAR ATAXIA 47" />
      </concept>
      <concept>
        <code value="OMIM:617933" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61" />
      </concept>
      <concept>
        <code value="OMIM:617935" />
        <display value="EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4" />
      </concept>
      <concept>
        <code value="OMIM:617936" />
        <display value="BUTYRYLCHOLINESTERASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:617938" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62" />
      </concept>
      <concept>
        <code value="OMIM:617941" />
        <display value="SHWACHMAN-DIAMOND SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:617948" />
        <display value="ELLIPTOCYTOSIS 3" />
      </concept>
      <concept>
        <code value="OMIM:617950" />
        <display value="COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36" />
      </concept>
      <concept>
        <code value="OMIM:617951" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 15" />
      </concept>
      <concept>
        <code value="OMIM:617952" />
        <display value="OSTEOGENESIS IMPERFECTA, TYPE XVIII" />
      </concept>
      <concept>
        <code value="OMIM:617953" />
        <display value="HYPERTHYROXINEMIA, EUTHYROID, CAUSED BY GENERALIZED 5-PRIME-DEIODINASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:617954" />
        <display value="MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:617955" />
        <display value="PHENYTOIN TOXICITY" />
      </concept>
      <concept>
        <code value="OMIM:617956" />
        <display value="BETA-GLUCOPYRANOSIDE TASTING" />
      </concept>
      <concept>
        <code value="OMIM:617959" />
        <display value="SPERMATOGENIC FAILURE 24" />
      </concept>
      <concept>
        <code value="OMIM:617960" />
        <display value="SPERMATOGENIC FAILURE 25" />
      </concept>
      <concept>
        <code value="OMIM:617961" />
        <display value="SPERMATOGENIC FAILURE 26" />
      </concept>
      <concept>
        <code value="OMIM:617964" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 16" />
      </concept>
      <concept>
        <code value="OMIM:617965" />
        <display value="SPERMATOGENIC FAILURE 27" />
      </concept>
      <concept>
        <code value="OMIM:617966" />
        <display value="LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 7" />
      </concept>
      <concept>
        <code value="OMIM:617967" />
        <display value="HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:617970" />
        <display value="RH-NULL, AMORPH TYPE" />
      </concept>
      <concept>
        <code value="OMIM:617971" />
        <display value="METHEMOGLOBINEMIA, BETA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:617973" />
        <display value="METHEMOGLOBINEMIA, ALPHA TYPE" />
      </concept>
      <concept>
        <code value="OMIM:617974" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE" />
      </concept>
      <concept>
        <code value="OMIM:617976" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63" />
      </concept>
      <concept>
        <code value="OMIM:617977" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:617980" />
        <display value="ERYTHROCYTOSIS, FAMILIAL, 6" />
      </concept>
      <concept>
        <code value="OMIM:617981" />
        <display value="ERYTHROCYTOSIS, FAMILIAL, 7" />
      </concept>
      <concept>
        <code value="OMIM:617982" />
        <display value="VERVERI-BRADY SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617983" />
        <display value="MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617984" />
        <display value="MICROCEPHALY 22, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617985" />
        <display value="MICROCEPHALY 23, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:617988" />
        <display value="JABERI-ELAHI SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:617991" />
        <display value="DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES" />
      </concept>
      <concept>
        <code value="OMIM:617992" />
        <display value="DEAFNESS, CONGENITAL HEART DEFECTS, AND POSTERIOR EMBRYOTOXON" />
      </concept>
      <concept>
        <code value="OMIM:617993" />
        <display value="TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2" />
      </concept>
      <concept>
        <code value="OMIM:617994" />
        <display value="TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3" />
      </concept>
      <concept>
        <code value="OMIM:617995" />
        <display value="IMPDH2 ENZYME ACTIVITY, VARIATION IN" />
      </concept>
      <concept>
        <code value="OMIM:617996" />
        <display value="OOCYTE MATURATION DEFECT 5" />
      </concept>
      <concept>
        <code value="OMIM:618000" />
        <display value="EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2" />
      </concept>
      <concept>
        <code value="OMIM:618003" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 57" />
      </concept>
      <concept>
        <code value="OMIM:618004" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64" />
      </concept>
      <concept>
        <code value="OMIM:618005" />
        <display value="CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION" />
      </concept>
      <concept>
        <code value="OMIM:618006" />
        <display value="LEUKODYSTROPHY, HYPOMYELINATING, 17" />
      </concept>
      <concept>
        <code value="OMIM:618007" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH BRAIN, LIVER, AND LUNG ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:618008" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65" />
      </concept>
      <concept>
        <code value="OMIM:618010" />
        <display value="GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17" />
      </concept>
      <concept>
        <code value="OMIM:618011" />
        <display value="HYPEREKPLEXIA 4" />
      </concept>
      <concept>
        <code value="OMIM:618012" />
        <display value="EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3" />
      </concept>
      <concept>
        <code value="OMIM:618013" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 109" />
      </concept>
      <concept>
        <code value="OMIM:618014" />
        <display value="PREMATURE OVARIAN FAILURE 14" />
      </concept>
      <concept>
        <code value="OMIM:618015" />
        <display value="PROTOPORPHYRIA, ERYTHROPOIETIC, 2" />
      </concept>
      <concept>
        <code value="OMIM:618018" />
        <display value="DRUG METABOLISM, ALTERED, CYP2C8-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:618019" />
        <display value="PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:618021" />
        <display value="TETRAAMELIA SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:618022" />
        <display value="HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:618026" />
        <display value="NOTCH2 N-TERMINAL-LIKE-RELATED, PSEUDOGENE" />
      </concept>
      <concept>
        <code value="OMIM:618027" />
        <display value="COFFIN-SIRIS SYNDROME 7" />
      </concept>
      <concept>
        <code value="OMIM:618031" />
        <display value="CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4" />
      </concept>
      <concept>
        <code value="OMIM:618036" />
        <display value="CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD" />
      </concept>
      <concept>
        <code value="OMIM:618042" />
        <display value="PULMONARY ALVEOLAR PROTEINOSIS WITH HYPOGAMMAGLOBULINEMIA" />
      </concept>
      <concept>
        <code value="OMIM:618048" />
        <display value="PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:618049" />
        <display value="PARKINSONISM-DYSTONIA, INFANTILE, 2" />
      </concept>
      <concept>
        <code value="OMIM:618050" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 57" />
      </concept>
      <concept>
        <code value="OMIM:618052" />
        <display value="CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27" />
      </concept>
      <concept>
        <code value="OMIM:618056" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:618057" />
        <display value="DRUG METABOLISM, ALTERED, CES1-RELATED" />
      </concept>
      <concept>
        <code value="OMIM:618060" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA" />
      </concept>
      <concept>
        <code value="OMIM:618061" />
        <display value="POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE" />
      </concept>
      <concept>
        <code value="OMIM:618063" />
        <display value="CILIARY DYSKINESIA, PRIMARY, 38" />
      </concept>
      <concept>
        <code value="OMIM:618065" />
        <display value="PONTOCEREBELLAR HYPOPLASIA, TYPE 1D" />
      </concept>
      <concept>
        <code value="OMIM:618067" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66" />
      </concept>
      <concept>
        <code value="OMIM:618074" />
        <display value="EPILEPSY, FAMILIAL ADULT MYOCLONIC, 6" />
      </concept>
      <concept>
        <code value="OMIM:618075" />
        <display value="EPILEPSY, FAMILIAL ADULT MYOCLONIC, 7" />
      </concept>
      <concept>
        <code value="OMIM:618076" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH" />
      </concept>
      <concept>
        <code value="OMIM:618077" />
        <display value="INFLAMMATORY BOWEL DISEASE 29" />
      </concept>
      <concept>
        <code value="OMIM:618078" />
        <display value="OVARIAN DYSGENESIS 6" />
      </concept>
      <concept>
        <code value="OMIM:618079" />
        <display value="LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 8" />
      </concept>
      <concept>
        <code value="OMIM:618084" />
        <display value="PEELING SKIN SYNDROME 6" />
      </concept>
      <concept>
        <code value="OMIM:618086" />
        <display value="SPERMATOGENIC FAILURE 28" />
      </concept>
      <concept>
        <code value="OMIM:618087" />
        <display value="SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS" />
      </concept>
      <concept>
        <code value="OMIM:618088" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:618089" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:618090" />
        <display value="NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM" />
      </concept>
      <concept>
        <code value="OMIM:618091" />
        <display value="SPERMATOGENIC FAILURE 29" />
      </concept>
      <concept>
        <code value="OMIM:618092" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES" />
      </concept>
      <concept>
        <code value="OMIM:618093" />
        <display value="SPINOCEREBELLAR ATAXIA 48" />
      </concept>
      <concept>
        <code value="OMIM:618094" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 110" />
      </concept>
      <concept>
        <code value="OMIM:618095" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 63" />
      </concept>
      <concept>
        <code value="OMIM:618096" />
        <display value="PREMATURE OVARIAN FAILURE 15" />
      </concept>
      <concept>
        <code value="OMIM:618097" />
        <display value="MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 2" />
      </concept>
      <concept>
        <code value="OMIM:618098" />
        <display value="PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5" />
      </concept>
      <concept>
        <code value="OMIM:618103" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64" />
      </concept>
      <concept>
        <code value="OMIM:618106" />
        <display value="MENTAL RETARDATION, AUTOSOMAL DOMINANT 58" />
      </concept>
      <concept>
        <code value="OMIM:618107" />
        <display value="OSTEOPETROSIS, AUTOSOMAL DOMINANT 3" />
      </concept>
      <concept>
        <code value="OMIM:618108" />
        <display value="IMMUNODEFICIENCY 57" />
      </concept>
      <concept>
        <code value="OMIM:618109" />
        <display value="MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65" />
      </concept>
      <concept>
        <code value="OMIM:618110" />
        <display value="SPERMATOGENIC FAILURE 30" />
      </concept>
      <concept>
        <code value="OMIM:618112" />
        <display value="SPERMATOGENIC FAILURE 31" />
      </concept>
      <concept>
        <code value="OMIM:618113" />
        <display value="ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION" />
      </concept>
      <concept>
        <code value="OMIM:618114" />
        <display value="LIDDLE SYNDROME 2" />
      </concept>
      <concept>
        <code value="OMIM:618115" />
        <display value="SPERMATOGENIC FAILURE 32" />
      </concept>
      <concept>
        <code value="OMIM:618116" />
        <display value="BONE MARROW FAILURE SYNDROME 4" />
      </concept>
      <concept>
        <code value="OMIM:618117" />
        <display value="OVARIAN DYSGENESIS 7" />
      </concept>
      <concept>
        <code value="OMIM:618120" />
        <display value="MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5" />
      </concept>
      <concept>
        <code value="OMIM:618123" />
        <display value="POLYDACTYLY, POSTAXIAL, TYPE A8" />
      </concept>
      <concept>
        <code value="OMIM:618124" />
        <display value="PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT" />
      </concept>
      <concept>
        <code value="OMIM:618126" />
        <display value="LIDDLE SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:618129" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4" />
      </concept>
      <concept>
        <code value="OMIM:618131" />
        <display value="IMMUNODEFICIENCY 58" />
      </concept>
      <concept>
        <code value="OMIM:618135" />
        <display value="MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8" />
      </concept>
      <concept>
        <code value="OMIM:618138" />
        <display value="MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23" />
      </concept>
      <concept>
        <code value="OMIM:618140" />
        <display value="DEAFNESS, AUTOSOMAL DOMINANT 74" />
      </concept>
      <concept>
        <code value="OMIM:618141" />
        <display value="EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67" />
      </concept>
      <concept>
        <code value="OMIM:618142" />
        <display value="MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:618143" />
        <display value="GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18" />
      </concept>
      <concept>
        <code value="OMIM:618144" />
        <display value="USHER SYNDROME, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:618145" />
        <display value="DEAFNESS, AUTOSOMAL RECESSIVE 111" />
      </concept>
      <concept>
        <code value="OMIM:618147" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES" />
      </concept>
      <concept>
        <code value="OMIM:618148" />
        <display value="EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:618149" />
        <display value="OROFACIAL CLEFT 8" />
      </concept>
      <concept>
        <code value="OMIM:618150" />
        <display value="SAUL-WILSON SYNDROME" />
      </concept>
      <concept>
        <code value="OMIM:618152" />
        <display value="SPERMATOGENIC FAILURE 33" />
      </concept>
      <concept>
        <code value="OMIM:618153" />
        <display value="SPERMATOGENIC FAILURE 34" />
      </concept>
      <concept>
        <code value="OMIM:618154" />
        <display value="HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3" />
      </concept>
      <concept>
        <code value="OMIM:618155" />
        <display value="OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES" />
      </concept>
      <concept>
        <code value="OMIM:618156" />
        <display value="SQUALENE SYNTHASE DEFICIENCY" />
      </concept>
      <concept>
        <code value="OMIM:618157" />
        <display value="ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV" />
      </concept>
      <concept>
        <code value="OMIM:618158" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY" />
      </concept>
      <concept>
        <code value="OMIM:618160" />
        <display value="ISOLATED GROWTH HORMONE DEFICIENCY, TYPE V" />
      </concept>
      <concept>
        <code value="OMIM:618161" />
        <display value="JOUBERT SYNDROME 35" />
      </concept>
      <concept>
        <code value="OMIM:618162" />
        <display value="SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE" />
      </concept>
      <concept>
        <code value="OMIM:618164" />
        <display value="CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY" />
      </concept>
      <concept>
        <code value="OMIM:618165" />
        <display value="BONE MARROW FAILURE SYNDROME 5" />
      </concept>
      <concept>
        <code value="OMIM:618167" />
        <display value="OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS" />
      </concept>
      <concept>
        <code value="OMIM:618168" />
        <display value="DIARRHEA 9" />
      </concept>
      <concept>
        <code value="OMIM:618170" />
        <display value="NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES" />
      </concept>
      <concept>
        <code value="OMIM:618173" />
        <display value="RETINITIS PIGMENTOSA 83" />
      </concept>
      <concept>
        <code value="OMIM:618174" />
        <display value="CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9" />
      </concept>
      <concept>
        <code value="OMIM:618176" />
        <display value="NEPHROTIC SYNDROME, TYPE 17" />
      </concept>
      <concept>
        <code value="OMIM:618177" />
        <display value="NEPHROTIC SYNDROME, TYPE 18" />
      </concept>
      <concept>
        <code value="OMIM:618178" />
        <display value="NEPHROTIC SYNDROME, TYPE 19" />
      </concept>
      <concept>
        <code value="OMIM:618179" />
        <display value="MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE" />
      </concept>
      <concept>
        <code value="OMIM:618180" />
        <display value="ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE WITH OR WITHOUT HYPOHIDROSIS" />
      </concept>
      <concept>
        <code value="OMIM:618182" />
        <display value="ORTHOSTATIC HYPOTENSION 2" />
      </concept>
      <concept>
        <code value="OMIM:618183" />
        <display value="DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE" />
      </concept>
      <concept>
        <code value="OMIM:618185" />
        <display value="PERIVENTRICULAR NODULAR HETEROTOPIA 8" />
      </concept>
      <concept>
        <code value="OMIM:618187" />
        <display value="OVARIAN DYSGENESIS 8" />
      </concept>
      <concept>
        <code value="OMIM:618188" />
        <display value="HYPERPARATHYROIDISM, TRANSIENT NEONATAL" />
      </concept>
      <concept>
        <code value="OMIM:618189" />
        <display value="CARDIOMYOPATHY, DILATED, 2C" />
      </concept>
      <concept>
        <code value="OMIM:618193" />
        <display value="POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2" />
      </concept>
      <concept>
        <code value="OMIM:618195" />
        <display value="INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA" />
      </concept>
      <concept>
        <code value="OMIM:618196" />
        <display value="CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2" />
      </concept>
      <concept>
        <code value="ORPHA:no_specific_disorder" />
        <display value="No specific disorder" />
      </concept>
      <concept>
        <code value="ORPHA:10" />
        <display value="48,XXYY syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:100" />
        <display value="Ataxia-telangiectasia" />
      </concept>
      <concept>
        <code value="ORPHA:1000" />
        <display value="Ocular albinism with late-onset sensorineural deafness" />
      </concept>
      <concept>
        <code value="ORPHA:100000" />
        <display value="Reticular perineurioma" />
      </concept>
      <concept>
        <code value="ORPHA:100001" />
        <display value="Sclerosing perineurioma" />
      </concept>
      <concept>
        <code value="ORPHA:100002" />
        <display value="Extraneural perineurioma" />
      </concept>
      <concept>
        <code value="ORPHA:100003" />
        <display value="Intraneural perineurioma" />
      </concept>
      <concept>
        <code value="ORPHA:100006" />
        <display value="ABeta amyloidosis, Dutch type" />
      </concept>
      <concept>
        <code value="ORPHA:100008" />
        <display value="ACys amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:100011" />
        <display value="Lissencephaly with cerebellar hypoplasia type A" />
      </concept>
      <concept>
        <code value="ORPHA:100012" />
        <display value="Lissencephaly with cerebellar hypoplasia type B" />
      </concept>
      <concept>
        <code value="ORPHA:100013" />
        <display value="Lissencephaly with cerebellar hypoplasia type C" />
      </concept>
      <concept>
        <code value="ORPHA:100014" />
        <display value="Lissencephaly with cerebellar hypoplasia type D" />
      </concept>
      <concept>
        <code value="ORPHA:100015" />
        <display value="Lissencephaly with cerebellar hypoplasia type E" />
      </concept>
      <concept>
        <code value="ORPHA:100016" />
        <display value="Lissencephaly with cerebellar hypoplasia type F" />
      </concept>
      <concept>
        <code value="ORPHA:100019" />
        <display value="Refractory anemia with excess blasts type 1" />
      </concept>
      <concept>
        <code value="ORPHA:100020" />
        <display value="Refractory anemia with excess blasts type 2" />
      </concept>
      <concept>
        <code value="ORPHA:100021" />
        <display value="Primary plasmacytoma of the bone" />
      </concept>
      <concept>
        <code value="ORPHA:100022" />
        <display value="Extramedullary soft tissue plasmacytoma" />
      </concept>
      <concept>
        <code value="ORPHA:100024" />
        <display value="Mu-heavy chain disease" />
      </concept>
      <concept>
        <code value="ORPHA:100025" />
        <display value="Alpha-heavy chain disease" />
      </concept>
      <concept>
        <code value="ORPHA:100026" />
        <display value="Gamma-heavy chain disease" />
      </concept>
      <concept>
        <code value="ORPHA:100031" />
        <display value="Hypoplastic amelogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:100032" />
        <display value="Hypocalcified amelogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:100033" />
        <display value="Hypomaturation amelogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:100034" />
        <display value="Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism" />
      </concept>
      <concept>
        <code value="ORPHA:100035" />
        <display value="Solitary necrotic nodule of the liver" />
      </concept>
      <concept>
        <code value="ORPHA:100043" />
        <display value="Autosomal dominant intermediate Charcot-Marie-Tooth disease type A" />
      </concept>
      <concept>
        <code value="ORPHA:100044" />
        <display value="Autosomal dominant intermediate Charcot-Marie-Tooth disease type B" />
      </concept>
      <concept>
        <code value="ORPHA:100045" />
        <display value="Autosomal dominant intermediate Charcot-Marie-Tooth disease type C" />
      </concept>
      <concept>
        <code value="ORPHA:100046" />
        <display value="Autosomal dominant intermediate Charcot-Marie-Tooth disease type D" />
      </concept>
      <concept>
        <code value="ORPHA:100047" />
        <display value="Esophageal duplication cyst" />
      </concept>
      <concept>
        <code value="ORPHA:100048" />
        <display value="Tubular duplication of the esophagus" />
      </concept>
      <concept>
        <code value="ORPHA:100049" />
        <display value="Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:100050" />
        <display value="Hereditary angioedema type 1" />
      </concept>
      <concept>
        <code value="ORPHA:100051" />
        <display value="Hereditary angioedema type 2" />
      </concept>
      <concept>
        <code value="ORPHA:100054" />
        <display value="Hereditary angioedema type 3" />
      </concept>
      <concept>
        <code value="ORPHA:100055" />
        <display value="Acquired angioedema type 2" />
      </concept>
      <concept>
        <code value="ORPHA:100056" />
        <display value="Acquired angioedema type 1" />
      </concept>
      <concept>
        <code value="ORPHA:100057" />
        <display value="Renin-angiotensin-aldosterone system-blocker-induced angioedema" />
      </concept>
      <concept>
        <code value="ORPHA:100067" />
        <display value="Waterhouse-Friderichsen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:100069" />
        <display value="Semantic dementia" />
      </concept>
      <concept>
        <code value="ORPHA:100070" />
        <display value="Progressive non-fluent aphasia" />
      </concept>
      <concept>
        <code value="ORPHA:100071" />
        <display value="Mosaic trisomy 3" />
      </concept>
      <concept>
        <code value="ORPHA:100073" />
        <display value="Neurogenic thoracic outlet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:100075" />
        <display value="Neuroendocrine tumor of stomach" />
      </concept>
      <concept>
        <code value="ORPHA:100076" />
        <display value="Duodenal neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100077" />
        <display value="Jejunal neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100078" />
        <display value="Ileal neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100079" />
        <display value="Neuroendocrine neoplasm of appendix" />
      </concept>
      <concept>
        <code value="ORPHA:100080" />
        <display value="Neuroendocrine tumor of the colon" />
      </concept>
      <concept>
        <code value="ORPHA:100081" />
        <display value="Neuroendocrine tumor of the rectum" />
      </concept>
      <concept>
        <code value="ORPHA:100082" />
        <display value="Neuroendocrine tumor of anal canal" />
      </concept>
      <concept>
        <code value="ORPHA:100083" />
        <display value="Laryngeal neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100084" />
        <display value="Middle ear neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100085" />
        <display value="Primary hepatic neuroendocrine carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:100086" />
        <display value="Gallbladder neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100087" />
        <display value="Thyroid tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100088" />
        <display value="Thyroid carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:100090" />
        <display value="Rare parathyroid tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100091" />
        <display value="Adrenal/paraganglial tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100092" />
        <display value="Gastroenteropancreatic neuroendocrine neoplasm" />
      </concept>
      <concept>
        <code value="ORPHA:100093" />
        <display value="Carcinoid syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:100094" />
        <display value="Multiple polyglandular tumor" />
      </concept>
      <concept>
        <code value="ORPHA:1001" />
        <display value="2q37 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:100100" />
        <display value="Thymic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:100101" />
        <display value="Neuroendocrine tumor with other location" />
      </concept>
      <concept>
        <code value="ORPHA:1003" />
        <display value="Scalp defects-postaxial polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1005" />
        <display value="Alopecia-contractures-dwarfism-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1006" />
        <display value="Alopecia antibody deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1008" />
        <display value="Alopecia-epilepsy-pyorrhea-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:100924" />
        <display value="Porphyria due to ALA dehydratase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:100973" />
        <display value="FRAXE intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:100974" />
        <display value="FRAXF syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:100976" />
        <display value="Bathing suit ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:100978" />
        <display value="Cloverleaf skull-asphyxiating thoracic dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:100979" />
        <display value="Autosomal dominant complex spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:100980" />
        <display value="Autosomal dominant pure spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:100981" />
        <display value="Autosomal recessive complex spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:100982" />
        <display value="Autosomal recessive pure spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:100984" />
        <display value="Autosomal dominant spastic paraplegia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:100985" />
        <display value="Autosomal dominant spastic paraplegia type 4" />
      </concept>
      <concept>
        <code value="ORPHA:100986" />
        <display value="Autosomal recessive spastic paraplegia type 5A" />
      </concept>
      <concept>
        <code value="ORPHA:100988" />
        <display value="Autosomal dominant spastic paraplegia type 6" />
      </concept>
      <concept>
        <code value="ORPHA:100989" />
        <display value="Autosomal dominant spastic paraplegia type 8" />
      </concept>
      <concept>
        <code value="ORPHA:100991" />
        <display value="Autosomal dominant spastic paraplegia type 10" />
      </concept>
      <concept>
        <code value="ORPHA:100993" />
        <display value="Autosomal dominant spastic paraplegia type 12" />
      </concept>
      <concept>
        <code value="ORPHA:100994" />
        <display value="Autosomal dominant spastic paraplegia type 13" />
      </concept>
      <concept>
        <code value="ORPHA:100995" />
        <display value="Autosomal recessive spastic paraplegia type 14" />
      </concept>
      <concept>
        <code value="ORPHA:100996" />
        <display value="Autosomal recessive spastic paraplegia type 15" />
      </concept>
      <concept>
        <code value="ORPHA:100997" />
        <display value="X-linked spastic paraplegia type 16" />
      </concept>
      <concept>
        <code value="ORPHA:100998" />
        <display value="Autosomal dominant spastic paraplegia type 17" />
      </concept>
      <concept>
        <code value="ORPHA:100999" />
        <display value="Autosomal dominant spastic paraplegia type 19" />
      </concept>
      <concept>
        <code value="ORPHA:101" />
        <display value="Dentatorubral pallidoluysian atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1010" />
        <display value="Autosomal dominant palmoplantar keratoderma and congenital alopecia" />
      </concept>
      <concept>
        <code value="ORPHA:101000" />
        <display value="Autosomal recessive spastic paraplegia type 20" />
      </concept>
      <concept>
        <code value="ORPHA:101001" />
        <display value="Autosomal recessive spastic paraplegia type 21" />
      </concept>
      <concept>
        <code value="ORPHA:101003" />
        <display value="Autosomal recessive spastic paraplegia type 23" />
      </concept>
      <concept>
        <code value="ORPHA:101004" />
        <display value="Autosomal recessive spastic paraplegia type 24" />
      </concept>
      <concept>
        <code value="ORPHA:101005" />
        <display value="Autosomal recessive spastic paraplegia type 25" />
      </concept>
      <concept>
        <code value="ORPHA:101006" />
        <display value="Autosomal recessive spastic paraplegia type 26" />
      </concept>
      <concept>
        <code value="ORPHA:101007" />
        <display value="Autosomal recessive spastic paraplegia type 27" />
      </concept>
      <concept>
        <code value="ORPHA:101008" />
        <display value="Autosomal recessive spastic paraplegia type 28" />
      </concept>
      <concept>
        <code value="ORPHA:101009" />
        <display value="Autosomal dominant spastic paraplegia type 29" />
      </concept>
      <concept>
        <code value="ORPHA:101010" />
        <display value="Autosomal spastic paraplegia type 30" />
      </concept>
      <concept>
        <code value="ORPHA:101011" />
        <display value="Autosomal dominant spastic paraplegia type 31" />
      </concept>
      <concept>
        <code value="ORPHA:101016" />
        <display value="Romano-Ward syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:101023" />
        <display value="Cleft hard palate" />
      </concept>
      <concept>
        <code value="ORPHA:101028" />
        <display value="Transaldolase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:101029" />
        <display value="Sub-cortical nodular heterotopia" />
      </concept>
      <concept>
        <code value="ORPHA:101030" />
        <display value="Subependymal nodular heterotopia" />
      </concept>
      <concept>
        <code value="ORPHA:101039" />
        <display value="Female restricted epilepsy with intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:101041" />
        <display value="Familial hypofibrinogenemia" />
      </concept>
      <concept>
        <code value="ORPHA:101043" />
        <display value="Aortic valve dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:101046" />
        <display value="Autosomal dominant epilepsy with auditory features" />
      </concept>
      <concept>
        <code value="ORPHA:101049" />
        <display value="Familial hypocalciuric hypercalcemia type 2" />
      </concept>
      <concept>
        <code value="ORPHA:101050" />
        <display value="Familial hypocalciuric hypercalcemia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:101063" />
        <display value="Situs inversus totalis" />
      </concept>
      <concept>
        <code value="ORPHA:101068" />
        <display value="Congenital stromal corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:101070" />
        <display value="Bilateral frontoparietal polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:101071" />
        <display value="Unilateral hemispheric polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:101075" />
        <display value="X-linked Charcot-Marie-Tooth disease type 1" />
      </concept>
      <concept>
        <code value="ORPHA:101076" />
        <display value="X-linked Charcot-Marie-Tooth disease type 2" />
      </concept>
      <concept>
        <code value="ORPHA:101077" />
        <display value="X-linked Charcot-Marie-Tooth disease type 3" />
      </concept>
      <concept>
        <code value="ORPHA:101078" />
        <display value="X-linked Charcot-Marie-Tooth disease type 4" />
      </concept>
      <concept>
        <code value="ORPHA:101081" />
        <display value="Charcot-Marie-Tooth disease type 1A" />
      </concept>
      <concept>
        <code value="ORPHA:101082" />
        <display value="Charcot-Marie-Tooth disease type 1B" />
      </concept>
      <concept>
        <code value="ORPHA:101083" />
        <display value="Charcot-Marie-Tooth disease type 1C" />
      </concept>
      <concept>
        <code value="ORPHA:101084" />
        <display value="Charcot-Marie-Tooth disease type 1D" />
      </concept>
      <concept>
        <code value="ORPHA:101085" />
        <display value="Charcot-Marie-Tooth disease type 1F" />
      </concept>
      <concept>
        <code value="ORPHA:101088" />
        <display value="X-linked hyper-IgM syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:101089" />
        <display value="Hyper-IgM syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:101090" />
        <display value="Hyper-IgM syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:101091" />
        <display value="Hyper-IgM syndrome type 4" />
      </concept>
      <concept>
        <code value="ORPHA:101092" />
        <display value="Hyper-IgM syndrome type 5" />
      </concept>
      <concept>
        <code value="ORPHA:101096" />
        <display value="Aregenerative anemia" />
      </concept>
      <concept>
        <code value="ORPHA:101097" />
        <display value="Autosomal recessive Charcot-Marie-Tooth disease with hoarseness" />
      </concept>
      <concept>
        <code value="ORPHA:101101" />
        <display value="Charcot-Marie-Tooth disease type 2B2" />
      </concept>
      <concept>
        <code value="ORPHA:101102" />
        <display value="Charcot-Marie-Tooth disease type 2H" />
      </concept>
      <concept>
        <code value="ORPHA:101104" />
        <display value="Marin-Amat syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:101106" />
        <display value="Non-secreting chemodectoma" />
      </concept>
      <concept>
        <code value="ORPHA:101108" />
        <display value="Spinocerebellar ataxia type 23" />
      </concept>
      <concept>
        <code value="ORPHA:101109" />
        <display value="Spinocerebellar ataxia type 28" />
      </concept>
      <concept>
        <code value="ORPHA:101110" />
        <display value="Spinocerebellar ataxia type 20" />
      </concept>
      <concept>
        <code value="ORPHA:101111" />
        <display value="Spinocerebellar ataxia type 25" />
      </concept>
      <concept>
        <code value="ORPHA:101112" />
        <display value="Spinocerebellar ataxia type 26" />
      </concept>
      <concept>
        <code value="ORPHA:101150" />
        <display value="Autosomal recessive dopa-responsive dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:101206" />
        <display value="Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:101330" />
        <display value="Porphyria cutanea tarda" />
      </concept>
      <concept>
        <code value="ORPHA:101334" />
        <display value="African tick typhus" />
      </concept>
      <concept>
        <code value="ORPHA:101351" />
        <display value="Familial isolated congenital asplenia" />
      </concept>
      <concept>
        <code value="ORPHA:1014" />
        <display value="Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:101433" />
        <display value="Rare urogenital disease" />
      </concept>
      <concept>
        <code value="ORPHA:101435" />
        <display value="Rare genetic eye disease" />
      </concept>
      <concept>
        <code value="ORPHA:101685" />
        <display value="Rare non-syndromic intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:1018" />
        <display value="X-linked diffuse leiomyomatosis-Alport syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:101932" />
        <display value="Anomaly of the mitral subvalvular apparatus" />
      </concept>
      <concept>
        <code value="ORPHA:101934" />
        <display value="Genetic cardiac rhythm disease" />
      </concept>
      <concept>
        <code value="ORPHA:101936" />
        <display value="Rare gastroesophageal disease" />
      </concept>
      <concept>
        <code value="ORPHA:101937" />
        <display value="Rare pancreatic disease" />
      </concept>
      <concept>
        <code value="ORPHA:101938" />
        <display value="Rare vascular liver disease" />
      </concept>
      <concept>
        <code value="ORPHA:101939" />
        <display value="Rare parenchymal liver disease" />
      </concept>
      <concept>
        <code value="ORPHA:101940" />
        <display value="Rare metabolic liver disease" />
      </concept>
      <concept>
        <code value="ORPHA:101941" />
        <display value="Rare biliary tract disease" />
      </concept>
      <concept>
        <code value="ORPHA:101943" />
        <display value="Rare hepatic and biliary tract tumor" />
      </concept>
      <concept>
        <code value="ORPHA:101944" />
        <display value="Rare pulmonary disease" />
      </concept>
      <concept>
        <code value="ORPHA:101945" />
        <display value="Rare bronchopulmonary tumor" />
      </concept>
      <concept>
        <code value="ORPHA:101950" />
        <display value="Rare eye tumor" />
      </concept>
      <concept>
        <code value="ORPHA:101952" />
        <display value="Rare diabetes mellitus" />
      </concept>
      <concept>
        <code value="ORPHA:101953" />
        <display value="Rare dyslipidemia" />
      </concept>
      <concept>
        <code value="ORPHA:101954" />
        <display value="Rare adrenal disease" />
      </concept>
      <concept>
        <code value="ORPHA:101955" />
        <display value="Rare thyroid disease" />
      </concept>
      <concept>
        <code value="ORPHA:101956" />
        <display value="Polyendocrinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:101957" />
        <display value="Pituitary deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:101958" />
        <display value="Primary adrenal insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:101959" />
        <display value="Chronic primary adrenal insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:101960" />
        <display value="Genetic chronic primary adrenal insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:101963" />
        <display value="Acquired chronic primary adrenal insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:101972" />
        <display value="Combined T and B cell immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:101977" />
        <display value="Immunodeficiency predominantly affecting antibody production" />
      </concept>
      <concept>
        <code value="ORPHA:101985" />
        <display value="Quantitative and/or qualitative congenital phagocyte defect" />
      </concept>
      <concept>
        <code value="ORPHA:101987" />
        <display value="Constitutional neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:101988" />
        <display value="Primary immunodeficiency due to a defect in innate immunity" />
      </concept>
      <concept>
        <code value="ORPHA:101992" />
        <display value="Immunodeficiency due to a complement cascade protein anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:101995" />
        <display value="Periodic fever syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:101997" />
        <display value="Primary immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:101998" />
        <display value="Rare epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:102" />
        <display value="Multiple system atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1020" />
        <display value="Early-onset autosomal dominant Alzheimer disease" />
      </concept>
      <concept>
        <code value="ORPHA:102000" />
        <display value="Medullar disease" />
      </concept>
      <concept>
        <code value="ORPHA:102002" />
        <display value="Rare ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:102003" />
        <display value="Rare movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:102005" />
        <display value="Brain inflammatory disease" />
      </concept>
      <concept>
        <code value="ORPHA:102006" />
        <display value="Neurovascular malformation" />
      </concept>
      <concept>
        <code value="ORPHA:102009" />
        <display value="Classic lissencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:102010" />
        <display value="Other syndrome with lissencephaly as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:102011" />
        <display value="Lissencephaly type 3" />
      </concept>
      <concept>
        <code value="ORPHA:102012" />
        <display value="Pure hereditary spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:102013" />
        <display value="Complex hereditary spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:102014" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:102015" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:102020" />
        <display value="Autosomal monosomy" />
      </concept>
      <concept>
        <code value="ORPHA:102021" />
        <display value="Rickettsial disease" />
      </concept>
      <concept>
        <code value="ORPHA:102022" />
        <display value="Spotted fever rickettsiosis" />
      </concept>
      <concept>
        <code value="ORPHA:102023" />
        <display value="Typhus-group rickettsiosis" />
      </concept>
      <concept>
        <code value="ORPHA:102024" />
        <display value="Human herpesvirus 8-related disorder" />
      </concept>
      <concept>
        <code value="ORPHA:1021" />
        <display value="Amaurosis-hypertrichosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:102237" />
        <display value="Unexplained periodic fever syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:102283" />
        <display value="Multiple congenital anomalies/dysmorphic syndrome-intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:102284" />
        <display value="Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:102285" />
        <display value="Multiple congenital anomalies/dysmorphic syndrome without intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:1023" />
        <display value="Congenital generalized hypertrichosis, Ambras type" />
      </concept>
      <concept>
        <code value="ORPHA:102369" />
        <display value="Rare syndromic intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:102373" />
        <display value="Primary glomerular disease" />
      </concept>
      <concept>
        <code value="ORPHA:102379" />
        <display value="Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent" />
      </concept>
      <concept>
        <code value="ORPHA:102381" />
        <display value="Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor" />
      </concept>
      <concept>
        <code value="ORPHA:1027" />
        <display value="Autosomal recessive amelia" />
      </concept>
      <concept>
        <code value="ORPHA:102724" />
        <display value="Acute myeloid leukemia with t(8;21)(q22;q22) translocation" />
      </concept>
      <concept>
        <code value="ORPHA:1028" />
        <display value="Ameloonychohypohidrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1031" />
        <display value="Enamel-renal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1032" />
        <display value="Hyperdibasic aminoaciduria type 1" />
      </concept>
      <concept>
        <code value="ORPHA:1035" />
        <display value="Beta-mercaptolactate cysteine disulfiduria" />
      </concept>
      <concept>
        <code value="ORPHA:1037" />
        <display value="Arthrogryposis multiplex congenita" />
      </concept>
      <concept>
        <code value="ORPHA:103907" />
        <display value="Chronic diarrhea due to glucoamylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:103908" />
        <display value="Congenital sodium diarrhea" />
      </concept>
      <concept>
        <code value="ORPHA:103909" />
        <display value="Trehalase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:103910" />
        <display value="Congenital enterocyte heparan sulfate deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:103918" />
        <display value="Tropical pancreatitis" />
      </concept>
      <concept>
        <code value="ORPHA:103919" />
        <display value="Autoimmune pancreatitis" />
      </concept>
      <concept>
        <code value="ORPHA:103920" />
        <display value="Undetermined colitis" />
      </concept>
      <concept>
        <code value="ORPHA:104" />
        <display value="Leber hereditary optic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:1040" />
        <display value="Metaphyseal anadysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:104003" />
        <display value="Congenital intestinal transport defect" />
      </concept>
      <concept>
        <code value="ORPHA:104004" />
        <display value="Intestinal disease due to vitamin absorption anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:104005" />
        <display value="Intestinal disease due to fat malabsorption" />
      </concept>
      <concept>
        <code value="ORPHA:104006" />
        <display value="Congenital intestinal disease due to an enzymatic defect" />
      </concept>
      <concept>
        <code value="ORPHA:104007" />
        <display value="Congenital enteropathy involving intestinal mucosa development" />
      </concept>
      <concept>
        <code value="ORPHA:104008" />
        <display value="Short bowel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:104009" />
        <display value="Rare disease involving intestinal motility" />
      </concept>
      <concept>
        <code value="ORPHA:104010" />
        <display value="Intestinal polyposis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:104011" />
        <display value="Rare tumor of intestine" />
      </concept>
      <concept>
        <code value="ORPHA:104012" />
        <display value="Rare inflammatory bowel disease" />
      </concept>
      <concept>
        <code value="ORPHA:104013" />
        <display value="Metabolic disease with intestinal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:104075" />
        <display value="Adenocarcinoma of the small instestine" />
      </concept>
      <concept>
        <code value="ORPHA:104076" />
        <display value="Leiomyosarcoma of small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:104077" />
        <display value="Myopathic intestinal pseudoobstruction" />
      </concept>
      <concept>
        <code value="ORPHA:104078" />
        <display value="Unclassified intestinal pseudoobstruction" />
      </concept>
      <concept>
        <code value="ORPHA:1041" />
        <display value="Hydrops fetalis" />
      </concept>
      <concept>
        <code value="ORPHA:1046" />
        <display value="Lethal hemolytic anemia-genital anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1047" />
        <display value="Sideroblastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:1048" />
        <display value="Isolated anencephaly/exencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:105" />
        <display value="Atresia of urethra" />
      </concept>
      <concept>
        <code value="ORPHA:1051" />
        <display value="Ramos-Arroyo syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1052" />
        <display value="Mosaic variegated aneuploidy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1053" />
        <display value="Vein of Galen aneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:1054" />
        <display value="Aneurysm of sinus of Valsalva" />
      </concept>
      <concept>
        <code value="ORPHA:1059" />
        <display value="Blue rubber bleb nevus" />
      </concept>
      <concept>
        <code value="ORPHA:1062" />
        <display value="Hereditary neurocutaneous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:1063" />
        <display value="Tufted angioma" />
      </concept>
      <concept>
        <code value="ORPHA:1064" />
        <display value="Aniridia-renal agenesis-psychomotor retardation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1065" />
        <display value="Aniridia-cerebellar ataxia-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1067" />
        <display value="Aniridia-ptosis-intellectual disability-familial obesity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1068" />
        <display value="Aniridia-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1069" />
        <display value="Aniridia-absent patella syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:107" />
        <display value="BOR syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1070" />
        <display value="Anisakiasis" />
      </concept>
      <concept>
        <code value="ORPHA:1071" />
        <display value="Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1072" />
        <display value="Ankyloblepharon filiforme adnatum-cleft palate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1074" />
        <display value="Ankyloblepharon filiforme adnatum-imperforate anus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1077" />
        <display value="Dental ankylosis" />
      </concept>
      <concept>
        <code value="ORPHA:1078" />
        <display value="Thumb stiffness-brachydactyly-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:108" />
        <display value="Babesiosis" />
      </concept>
      <concept>
        <code value="ORPHA:1081" />
        <display value="Coronary artery congenital malformation" />
      </concept>
      <concept>
        <code value="ORPHA:1083" />
        <display value="Microlissencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:1084" />
        <display value="Isolated lissencephaly type 1 without known genetic defects" />
      </concept>
      <concept>
        <code value="ORPHA:108959" />
        <display value="Non-syndromic esophageal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108961" />
        <display value="Syndromic esophageal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108963" />
        <display value="Non-syndromic gastroduodenal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108965" />
        <display value="Syndromic gastroduodenal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108967" />
        <display value="Non-syndromic intestinal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108969" />
        <display value="Syndromic intestinal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108971" />
        <display value="Non-syndromic visceral malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108973" />
        <display value="Syndromic visceral malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108977" />
        <display value="Non-syndromic diaphragmatic or abdominal wall malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108979" />
        <display value="Syndromic diaphragmatic or abdominal wall malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108989" />
        <display value="Non-syndromic central nervous system malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108991" />
        <display value="Syndrome with a central nervous system malformation as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:108993" />
        <display value="Non-syndromic respiratory or mediastinal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108995" />
        <display value="Syndromic respiratory or mediastinal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:108997" />
        <display value="Rare anemia" />
      </concept>
      <concept>
        <code value="ORPHA:108999" />
        <display value="Rare disorder due to toxic effects" />
      </concept>
      <concept>
        <code value="ORPHA:109" />
        <display value="Bannayan-Riley-Ruvalcaba syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:109007" />
        <display value="Arthrogryposis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:109009" />
        <display value="Syndrome with limb malformations as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:109011" />
        <display value="Non-syndromic limb malformation" />
      </concept>
      <concept>
        <code value="ORPHA:1094" />
        <display value="Anonychia-microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:11" />
        <display value="Pentasomy X" />
      </concept>
      <concept>
        <code value="ORPHA:110" />
        <display value="Bardet-Biedl syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1101" />
        <display value="Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1104" />
        <display value="Anophthalmia plus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1106" />
        <display value="Microphthalmia with limb anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:111" />
        <display value="Barth syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1110" />
        <display value="Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1112" />
        <display value="Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1113" />
        <display value="Aphalangy-syndactyly-microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1114" />
        <display value="Aplasia cutis congenita" />
      </concept>
      <concept>
        <code value="ORPHA:1115" />
        <display value="Recessive aplasia cutis congenita of limbs" />
      </concept>
      <concept>
        <code value="ORPHA:1116" />
        <display value="Aplasia cutis congenita-intestinal lymphangiectasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1117" />
        <display value="Aplasia cutis-myopia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1118" />
        <display value="Fibular aplasia-ectrodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:112" />
        <display value="Bartter syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1120" />
        <display value="Lung agenesis-heart defect-thumb anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1121" />
        <display value="Radial deficiency-tibial hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1122" />
        <display value="Ulnar hypoplasia-split foot syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1123" />
        <display value="Caudal appendage-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1125" />
        <display value="Ocular motor apraxia, Cogan type" />
      </concept>
      <concept>
        <code value="ORPHA:1126" />
        <display value="Aprosencephaly cerebellar dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:1129" />
        <display value="Arachnodactyly-abnormal ossification-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:113" />
        <display value="Bazex-Dupre-Christol syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1130" />
        <display value="Arachnodactyly-intellectual disability-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1131" />
        <display value="X-linked mandibulofacial dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:1132" />
        <display value="Aortic arch defects" />
      </concept>
      <concept>
        <code value="ORPHA:1133" />
        <display value="AREDYLD syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1134" />
        <display value="Isolated arrhinia" />
      </concept>
      <concept>
        <code value="ORPHA:1135" />
        <display value="Arrhinia-choanal atresia-microphthalmia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1136" />
        <display value="Arnold-Chiari malformation type II" />
      </concept>
      <concept>
        <code value="ORPHA:1138" />
        <display value="Abnormal origin of the pulmonary artery" />
      </concept>
      <concept>
        <code value="ORPHA:114" />
        <display value="Auriculoosteodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1143" />
        <display value="Neurogenic arthrogryposis multiplex congenita" />
      </concept>
      <concept>
        <code value="ORPHA:1144" />
        <display value="Arthrogryposis-like hand anomaly-sensorineural deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1145" />
        <display value="Infantile-onset X-linked spinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1146" />
        <display value="Digitotalar dysmorphism" />
      </concept>
      <concept>
        <code value="ORPHA:1147" />
        <display value="Sheldon-Hall syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1149" />
        <display value="Arthrogryposis-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:115" />
        <display value="Congenital contractural arachnodactyly" />
      </concept>
      <concept>
        <code value="ORPHA:1150" />
        <display value="Arthrogryposis multiplex congenita-whistling face syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1154" />
        <display value="Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1159" />
        <display value="Progressive pseudorheumatoid arthropathy of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:116" />
        <display value="Beckwith-Wiedemann syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1160" />
        <display value="Chylous ascites" />
      </concept>
      <concept>
        <code value="ORPHA:1163" />
        <display value="Aspergillosis" />
      </concept>
      <concept>
        <code value="ORPHA:1164" />
        <display value="Allergic bronchopulmonary aspergillosis" />
      </concept>
      <concept>
        <code value="ORPHA:1166" />
        <display value="Congenital unilateral hypoplasia of depressor anguli oris" />
      </concept>
      <concept>
        <code value="ORPHA:1168" />
        <display value="Ataxia-oculomotor apraxia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:117" />
        <display value="Behcet disease" />
      </concept>
      <concept>
        <code value="ORPHA:1170" />
        <display value="Autosomal recessive cerebelloparenchymal disorder type 3" />
      </concept>
      <concept>
        <code value="ORPHA:1171" />
        <display value="Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1172" />
        <display value="Autosomal recessive cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:1173" />
        <display value="Cerebellar ataxia-hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1174" />
        <display value="Cerebellar ataxia-ectodermal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1175" />
        <display value="X-linked progressive cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:117569" />
        <display value="Rare intestinal disease" />
      </concept>
      <concept>
        <code value="ORPHA:117573" />
        <display value="Syndromic anorectal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:1177" />
        <display value="Early-onset cerebellar ataxia with retained tendon reflexes" />
      </concept>
      <concept>
        <code value="ORPHA:1178" />
        <display value="Ataxia-tapetoretinal degeneration syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1179" />
        <display value="Benign paroxysmal tonic upgaze of childhood with ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:118" />
        <display value="Beta-mannosidosis" />
      </concept>
      <concept>
        <code value="ORPHA:1180" />
        <display value="Ataxia-hypogonadism-choroidal dystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1182" />
        <display value="Spastic ataxia with congenital miosis" />
      </concept>
      <concept>
        <code value="ORPHA:1183" />
        <display value="Opsoclonus-myoclonus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1184" />
        <display value="Ataxia-photosensitivity-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1185" />
        <display value="Spinocerebellar ataxia-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1186" />
        <display value="Infantile onset spinocerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:1187" />
        <display value="Lethal ataxia with deafness and optic atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1188" />
        <display value="Ataxia-deafness-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:119" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2E" />
      </concept>
      <concept>
        <code value="ORPHA:1190" />
        <display value="Atelosteogenesis type I" />
      </concept>
      <concept>
        <code value="ORPHA:1192" />
        <display value="Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1193" />
        <display value="Atkin-Flaitz syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1194" />
        <display value="TMEM70-related mitochondrial encephalo-cardio-myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1195" />
        <display value="Congenital atransferrinemia" />
      </concept>
      <concept>
        <code value="ORPHA:1198" />
        <display value="Colonic atresia" />
      </concept>
      <concept>
        <code value="ORPHA:1199" />
        <display value="Esophageal atresia" />
      </concept>
      <concept>
        <code value="ORPHA:1200" />
        <display value="Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1201" />
        <display value="Atresia of small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:1202" />
        <display value="Larynx atresia" />
      </concept>
      <concept>
        <code value="ORPHA:1203" />
        <display value="Duodenal atresia" />
      </concept>
      <concept>
        <code value="ORPHA:1205" />
        <display value="Mitral atresia" />
      </concept>
      <concept>
        <code value="ORPHA:1207" />
        <display value="Pulmonary atresia with ventricular septal defect" />
      </concept>
      <concept>
        <code value="ORPHA:1208" />
        <display value="Pulmonary atresia-intact ventricular septum syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1209" />
        <display value="Tricuspid atresia" />
      </concept>
      <concept>
        <code value="ORPHA:1214" />
        <display value="Progressive hemifacial atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1215" />
        <display value="Autosomal dominant optic atrophy plus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1216" />
        <display value="Autosomal dominant congenital benign spinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1217" />
        <display value="Spinal atrophy-ophthalmoplegia-pyramidal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:122" />
        <display value="Birt-Hogg-Dube syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1221" />
        <display value="Cheilitis glandularis" />
      </concept>
      <concept>
        <code value="ORPHA:1223" />
        <display value="Balantidiasis" />
      </concept>
      <concept>
        <code value="ORPHA:1225" />
        <display value="Baller-Gerold syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1226" />
        <display value="Bamforth-Lazarus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1227" />
        <display value="Bangstad syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1228" />
        <display value="Banki syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1229" />
        <display value="Congenital intrauterine infection-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:123" />
        <display value="Bjornstad syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1231" />
        <display value="Barber-Say syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1234" />
        <display value="Bartsocas-Papas syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1236" />
        <display value="Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1237" />
        <display value="Beemer-Ertbruggen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:124" />
        <display value="Blackfan-Diamond anemia" />
      </concept>
      <concept>
        <code value="ORPHA:1240" />
        <display value="Metaphyseal acroscyphodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1241" />
        <display value="Bencze syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1243" />
        <display value="Best vitelliform macular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1246" />
        <display value="Brachydactyly-nystagmus-cerebellar ataxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1247" />
        <display value="Schistosomiasis" />
      </concept>
      <concept>
        <code value="ORPHA:1248" />
        <display value="Maxillonasal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:125" />
        <display value="Bloom syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1252" />
        <display value="Blepharonasofacial malformation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1253" />
        <display value="Ascher syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1259" />
        <display value="Blepharoptosis-myopia-ectopia lentis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:126" />
        <display value="Blepharophimosis-epicanthus inversus-ptosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1260" />
        <display value="Sino-auricular heart block" />
      </concept>
      <concept>
        <code value="ORPHA:1261" />
        <display value="Bonnemann-Meinecke-Reich syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1262" />
        <display value="Book syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1263" />
        <display value="Boomerang dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1264" />
        <display value="Tricho-retino-dento-digital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1267" />
        <display value="Botulism" />
      </concept>
      <concept>
        <code value="ORPHA:127" />
        <display value="Borjeson-Forssman-Lehmann syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1270" />
        <display value="Bowen-Conradi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1272" />
        <display value="Ayme-Gripp syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1275" />
        <display value="Brachydactyly-elbow wrist dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1276" />
        <display value="Brachydactyly-arterial hypertension syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1277" />
        <display value="Brachydactyly-mesomelia-intellectual disability-heart defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1278" />
        <display value="Brachydactyly-preaxial hallux varus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:128" />
        <display value="Diphyllobothriasis" />
      </concept>
      <concept>
        <code value="ORPHA:129" />
        <display value="Pseudopelade of Brocq" />
      </concept>
      <concept>
        <code value="ORPHA:1292" />
        <display value="Brachymorphism-onychodysplasia-dysphalangism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1293" />
        <display value="Brachyolmia" />
      </concept>
      <concept>
        <code value="ORPHA:1295" />
        <display value="Brachytelephalangy-dysmorphism-Kallmann syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1296" />
        <display value="Lambert syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1297" />
        <display value="Branchio-oculo-facial syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1299" />
        <display value="Branchioskeletogenital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:13" />
        <display value="6-pyruvoyl-tetrahydropterin synthase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:130" />
        <display value="Brugada syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1300" />
        <display value="Autosomal dominant popliteal pterygium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1302" />
        <display value="Cryptogenic organizing pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:1303" />
        <display value="Bronchiolitis obliterans with obstructive pulmonary disease" />
      </concept>
      <concept>
        <code value="ORPHA:1304" />
        <display value="Brucellosis" />
      </concept>
      <concept>
        <code value="ORPHA:1305" />
        <display value="Feingold syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1306" />
        <display value="Buschke-Ollendorff syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1307" />
        <display value="Distal limb deficiencies-micrognathia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1308" />
        <display value="C syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1309" />
        <display value="Medullary sponge kidney" />
      </concept>
      <concept>
        <code value="ORPHA:131" />
        <display value="Budd-Chiari syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1310" />
        <display value="Caffey disease" />
      </concept>
      <concept>
        <code value="ORPHA:1313" />
        <display value="Infantile choroidocerebral calcification syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1314" />
        <display value="Symmetrical thalamic calcifications" />
      </concept>
      <concept>
        <code value="ORPHA:1318" />
        <display value="Campomelia, Cumming type" />
      </concept>
      <concept>
        <code value="ORPHA:1319" />
        <display value="Camptobrachydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:132" />
        <display value="Butyrylcholinesterase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1320" />
        <display value="Idiopathic camptocormia" />
      </concept>
      <concept>
        <code value="ORPHA:1321" />
        <display value="Camptodactyly-fibrous tissue hyperplasia-skeletal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1323" />
        <display value="Camptodactyly-joint contractures-facial skeletal defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1325" />
        <display value="Camptodactyly-taurinuria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1326" />
        <display value="Camptodactyly syndrome, Guadalajara type 2" />
      </concept>
      <concept>
        <code value="ORPHA:1327" />
        <display value="Camptodactyly syndrome, Guadalajara type 1" />
      </concept>
      <concept>
        <code value="ORPHA:1328" />
        <display value="Camurati-Engelmann disease" />
      </concept>
      <concept>
        <code value="ORPHA:1329" />
        <display value="Complete atrioventricular canal" />
      </concept>
      <concept>
        <code value="ORPHA:133" />
        <display value="Chronic beryllium disease" />
      </concept>
      <concept>
        <code value="ORPHA:1330" />
        <display value="Partial atrioventricular canal" />
      </concept>
      <concept>
        <code value="ORPHA:1331" />
        <display value="Familial prostate cancer" />
      </concept>
      <concept>
        <code value="ORPHA:1332" />
        <display value="Medullary thyroid carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:1333" />
        <display value="Familial pancreatic carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:1334" />
        <display value="Chronic mucocutaneous candidiasis" />
      </concept>
      <concept>
        <code value="ORPHA:1335" />
        <display value="Pentalogy of Cantrell" />
      </concept>
      <concept>
        <code value="ORPHA:1336" />
        <display value="Hyperkeratosis-hyperpigmentation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1338" />
        <display value="Heart defect-tongue hamartoma-polysyndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:134" />
        <display value="Beta-ketothiolase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1340" />
        <display value="Cardiofaciocutaneous syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1342" />
        <display value="Heart-hand syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:1344" />
        <display value="Atrial standstill" />
      </concept>
      <concept>
        <code value="ORPHA:1345" />
        <display value="Cardiomyopathy-cataract-hip spine disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1349" />
        <display value="Mitochondrial DNA-related cardiomyopathy and hearing loss" />
      </concept>
      <concept>
        <code value="ORPHA:135" />
        <display value="CACH syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1350" />
        <display value="Heart-hand syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:1352" />
        <display value="Atrioventricular defect-blepharophimosis-radial and anal defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1354" />
        <display value="Heart defects-limb shortening syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1355" />
        <display value="Congenital heart defect-round face-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1358" />
        <display value="Carey-Fineman-Ziter  syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1359" />
        <display value="Carney complex" />
      </concept>
      <concept>
        <code value="ORPHA:136" />
        <display value="CADASIL" />
      </concept>
      <concept>
        <code value="ORPHA:1361" />
        <display value="Carnosinemia" />
      </concept>
      <concept>
        <code value="ORPHA:1366" />
        <display value="Autosomal recessive palmoplantar keratoderma and congenital alopecia" />
      </concept>
      <concept>
        <code value="ORPHA:1368" />
        <display value="Cataract-ataxia-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1369" />
        <display value="Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137" />
        <display value="Congenital disorder of glycosylation" />
      </concept>
      <concept>
        <code value="ORPHA:1373" />
        <display value="Cataract-aberrant oral frenula-growth delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1375" />
        <display value="Cataract-hypertrichosis-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137577" />
        <display value="Neonatal hypoxic and ischemic brain injury" />
      </concept>
      <concept>
        <code value="ORPHA:137583" />
        <display value="Vulvar intraepithelial neoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:137586" />
        <display value="Herpes simplex virus keratitis" />
      </concept>
      <concept>
        <code value="ORPHA:137593" />
        <display value="Infectious epithelial keratitis" />
      </concept>
      <concept>
        <code value="ORPHA:137596" />
        <display value="Neurotrophic keratopathy" />
      </concept>
      <concept>
        <code value="ORPHA:137599" />
        <display value="Stromal keratitis" />
      </concept>
      <concept>
        <code value="ORPHA:137602" />
        <display value="Endotheliitis" />
      </concept>
      <concept>
        <code value="ORPHA:137605" />
        <display value="Legius syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137608" />
        <display value="Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137617" />
        <display value="Nephrogenic systemic fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:137622" />
        <display value="Intractable diarrhea-choanal atresia-eye anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137625" />
        <display value="Glycogen storage disease due to muscle and heart glycogen synthase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:137628" />
        <display value="Cardiac anomalies-heterotaxy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137631" />
        <display value="Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137634" />
        <display value="Overgrowth-macrocephaly-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137639" />
        <display value="Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137667" />
        <display value="Capillary malformation-arteriovenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:137672" />
        <display value="Pellucid marginal degeneration" />
      </concept>
      <concept>
        <code value="ORPHA:137675" />
        <display value="Histiocytoid cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:137678" />
        <display value="Czech dysplasia, metatarsal type" />
      </concept>
      <concept>
        <code value="ORPHA:137681" />
        <display value="Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1" />
      </concept>
      <concept>
        <code value="ORPHA:137686" />
        <display value="Asherman syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1377" />
        <display value="Cataract-microcornea syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137754" />
        <display value="Neurological conditions associated with aminoacylase 1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:137776" />
        <display value="Lethal congenital contracture syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:137783" />
        <display value="Lethal congenital contracture syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:137807" />
        <display value="Primary cutaneous amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:137810" />
        <display value="Nodular cutaneous amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:137814" />
        <display value="Macular amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:137817" />
        <display value="Arachnoiditis" />
      </concept>
      <concept>
        <code value="ORPHA:137820" />
        <display value="Extrapelvic endometriosis" />
      </concept>
      <concept>
        <code value="ORPHA:137831" />
        <display value="X-linked intellectual disability-cerebellar hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137834" />
        <display value="Frank-Ter Haar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137839" />
        <display value="Lemierre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137867" />
        <display value="Madras motor neuron disease" />
      </concept>
      <concept>
        <code value="ORPHA:137888" />
        <display value="Auriculocondylar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137893" />
        <display value="Male infertility due to large-headed multiflagellar polyploid spermatozoa" />
      </concept>
      <concept>
        <code value="ORPHA:137898" />
        <display value="Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137902" />
        <display value="Isolated optic nerve hypoplasia/aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:137905" />
        <display value="Syndromic optic nerve hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:137908" />
        <display value="Hypotonia with lactic acidemia and hyperammonemia" />
      </concept>
      <concept>
        <code value="ORPHA:137911" />
        <display value="Autism-facial port-wine stain syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:137914" />
        <display value="Choanal atresia" />
      </concept>
      <concept>
        <code value="ORPHA:137917" />
        <display value="Choanal atresia, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:137920" />
        <display value="Choanal atresia, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:137926" />
        <display value="Primary laryngeal lymphangioma" />
      </concept>
      <concept>
        <code value="ORPHA:137929" />
        <display value="Neonatal brainstem dysfunction" />
      </concept>
      <concept>
        <code value="ORPHA:137932" />
        <display value="Congenital laryngeal palsy" />
      </concept>
      <concept>
        <code value="ORPHA:137935" />
        <display value="Laryngotracheal angioma" />
      </concept>
      <concept>
        <code value="ORPHA:138" />
        <display value="CHARGE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1380" />
        <display value="Cataract-nephropathy-encephalopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:138041" />
        <display value="Pierre Robin syndrome associated with collagen disease" />
      </concept>
      <concept>
        <code value="ORPHA:138044" />
        <display value="Rare disease with Pierre Robin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:138047" />
        <display value="Pierre Robin syndrome associated with a chromosomal anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:138050" />
        <display value="Pierre Robin syndrome associated with branchial archs anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:138055" />
        <display value="Pierre Robin syndrome associated with bone disease" />
      </concept>
      <concept>
        <code value="ORPHA:138059" />
        <display value="Teratogenic Pierre Robin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1381" />
        <display value="Cataract-intellectual disability-anal atresia-urinary defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1383" />
        <display value="Cataract-deafness-hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1387" />
        <display value="Cataract-intellectual disability-hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1388" />
        <display value="Catel-Manzke syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1389" />
        <display value="Cortical blindness-intellectual disability-polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139" />
        <display value="CHILD syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1390" />
        <display value="Night blindness-skeletal anomalies-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139009" />
        <display value="Developmental anomaly of metabolic origin" />
      </concept>
      <concept>
        <code value="ORPHA:139012" />
        <display value="Rare bone development disorder" />
      </concept>
      <concept>
        <code value="ORPHA:139021" />
        <display value="Malformation syndrome with short stature" />
      </concept>
      <concept>
        <code value="ORPHA:139024" />
        <display value="Overgrowth/obesity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139027" />
        <display value="Malformation syndrome with skin/mucosae involvement" />
      </concept>
      <concept>
        <code value="ORPHA:139030" />
        <display value="Rare developmental defect with connective tissue involvement" />
      </concept>
      <concept>
        <code value="ORPHA:139033" />
        <display value="Progeroid syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139036" />
        <display value="Branchial arch or oral-acral syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139039" />
        <display value="Orofacial clefting syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139042" />
        <display value="Malformation syndrome with odontal and/or periodontal component" />
      </concept>
      <concept>
        <code value="ORPHA:1393" />
        <display value="Cerebrocostomandibular syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139390" />
        <display value="Isolated craniosynostosis" />
      </concept>
      <concept>
        <code value="ORPHA:139393" />
        <display value="Syndromic craniosynostosis" />
      </concept>
      <concept>
        <code value="ORPHA:139396" />
        <display value="X-linked cerebral adrenoleukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:139399" />
        <display value="Adrenomyeloneuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:1394" />
        <display value="Cerebrofaciothoracic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:139402" />
        <display value="Drug rash with eosinophilia and systemic symptoms" />
      </concept>
      <concept>
        <code value="ORPHA:139406" />
        <display value="Encephalopathy due to prosaposin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:139411" />
        <display value="Carney triad" />
      </concept>
      <concept>
        <code value="ORPHA:139414" />
        <display value="Congenital panfollicular nevus" />
      </concept>
      <concept>
        <code value="ORPHA:139417" />
        <display value="Acute transverse myelitis" />
      </concept>
      <concept>
        <code value="ORPHA:139420" />
        <display value="Secondary acute transverse myelitis" />
      </concept>
      <concept>
        <code value="ORPHA:139423" />
        <display value="Idiopathic acute transverse myelitis" />
      </concept>
      <concept>
        <code value="ORPHA:139426" />
        <display value="Perioral myoclonia with absences" />
      </concept>
      <concept>
        <code value="ORPHA:139431" />
        <display value="Jeavons syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139436" />
        <display value="Multicentric reticulohistiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:139441" />
        <display value="Hypomyelination with atrophy of basal ganglia and cerebellum" />
      </concept>
      <concept>
        <code value="ORPHA:139444" />
        <display value="Leukoencephalopathy with bilateral anterior temporal lobe cysts" />
      </concept>
      <concept>
        <code value="ORPHA:139447" />
        <display value="Progressive cavitating leukoencephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:139450" />
        <display value="Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139455" />
        <display value="Autosomal recessive bestrophinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:139466" />
        <display value="SERKAL syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139471" />
        <display value="Microphthalmia with brain and digit anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:139474" />
        <display value="17q11.2 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:139480" />
        <display value="Autosomal recessive spastic paraplegia type 39" />
      </concept>
      <concept>
        <code value="ORPHA:139485" />
        <display value="Autosomal recessive ataxia due to ubiquinone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:139491" />
        <display value="Hemochromatosis type 4" />
      </concept>
      <concept>
        <code value="ORPHA:139507" />
        <display value="African iron overload" />
      </concept>
      <concept>
        <code value="ORPHA:139512" />
        <display value="Neuropathy with hearing impairment" />
      </concept>
      <concept>
        <code value="ORPHA:139515" />
        <display value="Charcot-Marie-Tooth disease type 4J" />
      </concept>
      <concept>
        <code value="ORPHA:139518" />
        <display value="Distal hereditary motor neuropathy type 1" />
      </concept>
      <concept>
        <code value="ORPHA:139525" />
        <display value="Distal hereditary motor neuropathy type 2" />
      </concept>
      <concept>
        <code value="ORPHA:139536" />
        <display value="Distal hereditary motor neuropathy type 5" />
      </concept>
      <concept>
        <code value="ORPHA:139547" />
        <display value="Distal spinal muscular atrophy type 3" />
      </concept>
      <concept>
        <code value="ORPHA:139552" />
        <display value="Distal hereditary motor neuropathy, Jerash type" />
      </concept>
      <concept>
        <code value="ORPHA:139557" />
        <display value="X-linked distal spinal muscular atrophy type 3" />
      </concept>
      <concept>
        <code value="ORPHA:139564" />
        <display value="Hereditary sensory and autonomic neuropathy type 1B" />
      </concept>
      <concept>
        <code value="ORPHA:139573" />
        <display value="Hereditary sensory and autonomic neuropathy with deafness and global delay" />
      </concept>
      <concept>
        <code value="ORPHA:139578" />
        <display value="Mutilating hereditary sensory neuropathy with spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:139583" />
        <display value="X-linked hereditary sensory and autonomic neuropathy with deafness" />
      </concept>
      <concept>
        <code value="ORPHA:139589" />
        <display value="Distal hereditary motor neuropathy type 7" />
      </concept>
      <concept>
        <code value="ORPHA:1396" />
        <display value="Cerebrorenodigital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1397" />
        <display value="Hydrocephaly-cerebellar agenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1398" />
        <display value="Isolated cerebellar agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:1399" />
        <display value="Richards-Rundle syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:14" />
        <display value="Abetalipoproteinemia" />
      </concept>
      <concept>
        <code value="ORPHA:140" />
        <display value="Campomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:140162" />
        <display value="Inherited cancer-predisposing syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140286" />
        <display value="Secondary hypoparathyroidism due to impaired parathormon secretion" />
      </concept>
      <concept>
        <code value="ORPHA:140436" />
        <display value="Primary intraosseous venous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:140453" />
        <display value="Autosomal dominant hereditary demyelinating motor and sensory neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:140456" />
        <display value="Autosomal dominant hereditary axonal motor and sensory neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:140459" />
        <display value="Autosomal recessive hereditary demyelinating motor and sensory neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:140465" />
        <display value="Autosomal dominant distal hereditary motor neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:140468" />
        <display value="Autosomal recessive distal hereditary motor neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:140471" />
        <display value="Hereditary sensory and autonomic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:140474" />
        <display value="Autosomal dominant hereditary sensory and autonomic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:140477" />
        <display value="Autosomal recessive hereditary sensory and autonomic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:140481" />
        <display value="Autosomal dominant slowed nerve conduction velocity" />
      </concept>
      <concept>
        <code value="ORPHA:1406" />
        <display value="Charlie M syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140653" />
        <display value="Neuro-ophthalmological disease" />
      </concept>
      <concept>
        <code value="ORPHA:1408" />
        <display value="Hair defect-photosensitivity-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140874" />
        <display value="Joubert syndrome and related disorders" />
      </concept>
      <concept>
        <code value="ORPHA:140896" />
        <display value="Acute respiratory coronavirus infection" />
      </concept>
      <concept>
        <code value="ORPHA:1409" />
        <display value="Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140905" />
        <display value="Hyperlipidemia due to hepatic triacylglycerol lipase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:140908" />
        <display value="Brachydactyly type B2" />
      </concept>
      <concept>
        <code value="ORPHA:140917" />
        <display value="Stapes ankylosis with broad thumbs and toes" />
      </concept>
      <concept>
        <code value="ORPHA:140922" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2J" />
      </concept>
      <concept>
        <code value="ORPHA:140927" />
        <display value="Benign familial neonatal-infantile seizures" />
      </concept>
      <concept>
        <code value="ORPHA:140933" />
        <display value="Linear atrophoderma of Moulin" />
      </concept>
      <concept>
        <code value="ORPHA:140936" />
        <display value="Lelis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140941" />
        <display value="Short stature due to primary acid-labile subunit deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:140944" />
        <display value="CLOVES syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140952" />
        <display value="Syndactyly-telecanthus-anogenital and renal malformations syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140957" />
        <display value="Autosomal dominant macrothrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:140963" />
        <display value="Bilateral microtia-deafness-cleft palate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140966" />
        <display value="Palmoplantar keratoderma, Nagashima type" />
      </concept>
      <concept>
        <code value="ORPHA:140969" />
        <display value="Saldino-Mainzer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140976" />
        <display value="RHYNS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:140989" />
        <display value="Primary central nervous system vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:140997" />
        <display value="Orofaciodigital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:141" />
        <display value="Canavan disease" />
      </concept>
      <concept>
        <code value="ORPHA:1410" />
        <display value="Uncombable hair syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:141000" />
        <display value="Orofaciodigital syndrome type 11" />
      </concept>
      <concept>
        <code value="ORPHA:141007" />
        <display value="Orofaciodigital syndrome type 9" />
      </concept>
      <concept>
        <code value="ORPHA:141013" />
        <display value="First branchial cleft anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:141022" />
        <display value="Second branchial cleft anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:141030" />
        <display value="Third branchial cleft anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:141037" />
        <display value="Fourth branchial cleft anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:141046" />
        <display value="Cervical dermoid cyst" />
      </concept>
      <concept>
        <code value="ORPHA:141051" />
        <display value="Facial dermoid cyst" />
      </concept>
      <concept>
        <code value="ORPHA:141061" />
        <display value="Commissural lip fistula" />
      </concept>
      <concept>
        <code value="ORPHA:141064" />
        <display value="Lower lip fistula" />
      </concept>
      <concept>
        <code value="ORPHA:141067" />
        <display value="Cervicofacial fibrochondroma" />
      </concept>
      <concept>
        <code value="ORPHA:141071" />
        <display value="Digestive duplication cyst of the tongue" />
      </concept>
      <concept>
        <code value="ORPHA:141074" />
        <display value="External auditory canal aplasia/hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:141077" />
        <display value="Epignathus" />
      </concept>
      <concept>
        <code value="ORPHA:141083" />
        <display value="Nasolacrimal duct cyst" />
      </concept>
      <concept>
        <code value="ORPHA:141091" />
        <display value="Polyrrhinia" />
      </concept>
      <concept>
        <code value="ORPHA:141096" />
        <display value="Supernumerary nostril" />
      </concept>
      <concept>
        <code value="ORPHA:141099" />
        <display value="Proboscis lateralis" />
      </concept>
      <concept>
        <code value="ORPHA:141103" />
        <display value="Nasal dermoid cyst" />
      </concept>
      <concept>
        <code value="ORPHA:141107" />
        <display value="Nasopharyngeal teratoma" />
      </concept>
      <concept>
        <code value="ORPHA:141112" />
        <display value="Nasal glial heterotopia" />
      </concept>
      <concept>
        <code value="ORPHA:141115" />
        <display value="Nasal ganglioglioma" />
      </concept>
      <concept>
        <code value="ORPHA:141118" />
        <display value="Nasal encephalocele" />
      </concept>
      <concept>
        <code value="ORPHA:141121" />
        <display value="Congenital subglottic stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:141124" />
        <display value="Congenital laryngeal cyst" />
      </concept>
      <concept>
        <code value="ORPHA:141127" />
        <display value="Congenital tracheal stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:141132" />
        <display value="Oculo-auriculo-vertebral spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:141136" />
        <display value="Otomandibular syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:141145" />
        <display value="Hemifacial hyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:141148" />
        <display value="Hemifacial myohyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:141152" />
        <display value="Isolated congenital hypoglossia/aglossia" />
      </concept>
      <concept>
        <code value="ORPHA:141163" />
        <display value="Glossopalatine ankylosis" />
      </concept>
      <concept>
        <code value="ORPHA:141168" />
        <display value="Frontonasal arteriovenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:141171" />
        <display value="Maxillary arteriovenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:141174" />
        <display value="Mandibular arteriovenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:141179" />
        <display value="Non-involuting congenital hemangioma" />
      </concept>
      <concept>
        <code value="ORPHA:141184" />
        <display value="Rapidly involuting congenital hemangioma" />
      </concept>
      <concept>
        <code value="ORPHA:141189" />
        <display value="Cerebrofacial arteriovenous metameric syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:141194" />
        <display value="Cerebrofacial arteriovenous metameric syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:141199" />
        <display value="Cerebrofacial arteriovenous metameric syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:1412" />
        <display value="Tarsal-carpal coalition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:141209" />
        <display value="Diffuse lymphatic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:141214" />
        <display value="Isolated congenital syngnathia" />
      </concept>
      <concept>
        <code value="ORPHA:141219" />
        <display value="Nasal dorsum fistula" />
      </concept>
      <concept>
        <code value="ORPHA:141229" />
        <display value="Facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141234" />
        <display value="Median facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141239" />
        <display value="Median cleft of the upper lip and maxilla" />
      </concept>
      <concept>
        <code value="ORPHA:141242" />
        <display value="Paramedian nasal cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141253" />
        <display value="Oblique facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141258" />
        <display value="Tessier number 4 facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141261" />
        <display value="Tessier number 5 facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141265" />
        <display value="Tessier number 6 facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141269" />
        <display value="Lateral facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141276" />
        <display value="Tessier number 7 facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141288" />
        <display value="Midline cervical cleft" />
      </concept>
      <concept>
        <code value="ORPHA:141291" />
        <display value="Cleft lip and alveolus" />
      </concept>
      <concept>
        <code value="ORPHA:141327" />
        <display value="Orofaciodigital syndrome type 12" />
      </concept>
      <concept>
        <code value="ORPHA:141330" />
        <display value="Orofaciodigital syndrome type 13" />
      </concept>
      <concept>
        <code value="ORPHA:141333" />
        <display value="Biemond syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:1414" />
        <display value="Cholestasis-lymphedema syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1415" />
        <display value="Cholestasis-pigmentary retinopathy-cleft palate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1416" />
        <display value="Familial calcium pyrophosphate deposition" />
      </concept>
      <concept>
        <code value="ORPHA:142" />
        <display value="Anaplastic thyroid carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:1422" />
        <display value="Chondrodysplasia-disorder of sex development syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1423" />
        <display value="Lethal recessive chondrodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1425" />
        <display value="Desbuquois syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1426" />
        <display value="Greenberg dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1427" />
        <display value="Otospondylomegaepiphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1428" />
        <display value="Familial chondromalacia patellae" />
      </concept>
      <concept>
        <code value="ORPHA:1429" />
        <display value="Benign hereditary chorea" />
      </concept>
      <concept>
        <code value="ORPHA:143" />
        <display value="Parathyroid carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:1431" />
        <display value="Paroxysmal dyskinesia" />
      </concept>
      <concept>
        <code value="ORPHA:1433" />
        <display value="Choroidal atrophy-alopecia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1434" />
        <display value="Choroideremia-hypopituitarism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1435" />
        <display value="Choroideremia-deafness-obesity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1436" />
        <display value="X-linked skeletal dysplasia-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1437" />
        <display value="Ring chromosome 1 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1438" />
        <display value="Ring chromosome 10 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1439" />
        <display value="Ring chromosome 12 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:144" />
        <display value="Lynch syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1440" />
        <display value="Ring chromosome 14 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1441" />
        <display value="Ring chromosome 17 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1442" />
        <display value="Ring chromosome 18 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1443" />
        <display value="Ring chromosome 19 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1444" />
        <display value="Ring chromosome 20 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1445" />
        <display value="Ring chromosome 21 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1446" />
        <display value="Ring chromosome 22 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1447" />
        <display value="Ring chromosome 4 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1448" />
        <display value="Ring chromosome 6 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1449" />
        <display value="Ring chromosome 7 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:145" />
        <display value="Hereditary breast and ovarian cancer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1450" />
        <display value="Ring chromosome 8 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1451" />
        <display value="CINCA syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1452" />
        <display value="Cleidocranial dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1453" />
        <display value="Cleidorhizomelic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1454" />
        <display value="Joubert syndrome with hepatic defect" />
      </concept>
      <concept>
        <code value="ORPHA:1455" />
        <display value="Autosomal dominant coarctation of aorta" />
      </concept>
      <concept>
        <code value="ORPHA:1456" />
        <display value="Atypical coarctation of aorta" />
      </concept>
      <concept>
        <code value="ORPHA:1457" />
        <display value="Aorta coarctation" />
      </concept>
      <concept>
        <code value="ORPHA:1458" />
        <display value="CODAS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1459" />
        <display value="Celiac disease-epilepsy-cerebral calcification syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:146" />
        <display value="Differentiated thyroid carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:1460" />
        <display value="Isolated complex III deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1461" />
        <display value="Criss-cross heart" />
      </concept>
      <concept>
        <code value="ORPHA:1463" />
        <display value="Triatrial heart" />
      </concept>
      <concept>
        <code value="ORPHA:1464" />
        <display value="Univentricular heart" />
      </concept>
      <concept>
        <code value="ORPHA:1465" />
        <display value="Coffin-Siris syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1466" />
        <display value="COFS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1467" />
        <display value="Cogan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:147" />
        <display value="Carbamoyl-phosphate synthetase 1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1471" />
        <display value="Coloboma of macula-brachydactyly type B syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1473" />
        <display value="Uveal coloboma-cleft lip and palate-intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:1475" />
        <display value="Renal coloboma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1478" />
        <display value="Interatrial communication" />
      </concept>
      <concept>
        <code value="ORPHA:1479" />
        <display value="Atrial septal defect-atrioventricular conduction defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:148" />
        <display value="Multiple carboxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1482" />
        <display value="Gonococcal conjunctivitis" />
      </concept>
      <concept>
        <code value="ORPHA:1484" />
        <display value="Contractures-ectodermal dysplasia-cleft lip/palate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1485" />
        <display value="Arthrogryposis-hyperkeratosis syndrome, lethal form" />
      </concept>
      <concept>
        <code value="ORPHA:1486" />
        <display value="Lethal congenital contracture syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:1487" />
        <display value="Cooks syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1488" />
        <display value="Cooper-Jabs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1489" />
        <display value="Whooping cough" />
      </concept>
      <concept>
        <code value="ORPHA:1490" />
        <display value="Corneal dystrophy-perceptive deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1493" />
        <display value="Vici syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1495" />
        <display value="Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1496" />
        <display value="Corpus callosum agenesis-neuronopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1497" />
        <display value="X-linked complicated corpus callosum dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:15" />
        <display value="Achondroplasia" />
      </concept>
      <concept>
        <code value="ORPHA:150" />
        <display value="Nasopharyngeal carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:1501" />
        <display value="Adrenocortical carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:1505" />
        <display value="Short rib-polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1506" />
        <display value="Thin ribs-tubular bones-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1507" />
        <display value="Autosomal recessive Robinow syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1508" />
        <display value="Coxoauricular syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1509" />
        <display value="Coxopodopatellar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1512" />
        <display value="Crane-Heise syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1513" />
        <display value="Craniodiaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1514" />
        <display value="Craniodigital-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1515" />
        <display value="Cranioectodermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1516" />
        <display value="Craniofacial dyssynostosis" />
      </concept>
      <concept>
        <code value="ORPHA:1517" />
        <display value="Hypertrichotic osteochondrodysplasia, Cantu type" />
      </concept>
      <concept>
        <code value="ORPHA:1519" />
        <display value="Hypertelorism, Teebi type" />
      </concept>
      <concept>
        <code value="ORPHA:1520" />
        <display value="Craniofrontonasal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1521" />
        <display value="Craniofrontonasal dysplasia-Poland anomaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1522" />
        <display value="Craniometaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1524" />
        <display value="Craniomicromelic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1525" />
        <display value="Cranio-osteoarthropathy" />
      </concept>
      <concept>
        <code value="ORPHA:1527" />
        <display value="Craniosynostosis, Philadelphia type" />
      </concept>
      <concept>
        <code value="ORPHA:1528" />
        <display value="Craniotelencephalic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1529" />
        <display value="Craniofacial-deafness-hand syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1530" />
        <display value="Craniosynostosis-cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1531" />
        <display value="Craniosynostosis" />
      </concept>
      <concept>
        <code value="ORPHA:1532" />
        <display value="Gomez-Lopez-Hernandez syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1533" />
        <display value="Craniosynostosis-fibular aplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1538" />
        <display value="Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:154" />
        <display value="Familial isolated dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1540" />
        <display value="Jackson-Weiss syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1541" />
        <display value="Craniosynostosis, Boston type" />
      </concept>
      <concept>
        <code value="ORPHA:1544" />
        <display value="Benign focal seizures of adolescence" />
      </concept>
      <concept>
        <code value="ORPHA:1545" />
        <display value="Crisponi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1546" />
        <display value="Cryptococcosis" />
      </concept>
      <concept>
        <code value="ORPHA:1547" />
        <display value="Cryptomicrotia-brachydactyly-excess fingertip arch syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1548" />
        <display value="Cryptorchidism-arachnodactyly-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1549" />
        <display value="Cryptosporidiosis" />
      </concept>
      <concept>
        <code value="ORPHA:1551" />
        <display value="Familial benign copper deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1552" />
        <display value="Currarino syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1553" />
        <display value="Curry-Jones syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1555" />
        <display value="Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1556" />
        <display value="Cutis marmorata telangiectatica congenita" />
      </concept>
      <concept>
        <code value="ORPHA:155832" />
        <display value="Rare head and neck malformation" />
      </concept>
      <concept>
        <code value="ORPHA:155835" />
        <display value="Cysts and fistulae of the face and oral cavity" />
      </concept>
      <concept>
        <code value="ORPHA:155838" />
        <display value="Pinnae fistula or cyst" />
      </concept>
      <concept>
        <code value="ORPHA:155867" />
        <display value="Paramedian facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:155878" />
        <display value="Submucosal cleft palate" />
      </concept>
      <concept>
        <code value="ORPHA:155884" />
        <display value="Coloboma of superior eyelid" />
      </concept>
      <concept>
        <code value="ORPHA:155889" />
        <display value="Coloboma of inferior eyelid" />
      </concept>
      <concept>
        <code value="ORPHA:155896" />
        <display value="Otomandibular dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:155899" />
        <display value="Mandibulofacial dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:156" />
        <display value="Carnitine palmitoyl transferase 1A deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1560" />
        <display value="Cysticercosis" />
      </concept>
      <concept>
        <code value="ORPHA:156005" />
        <display value="Primary early-onset glaucoma" />
      </concept>
      <concept>
        <code value="ORPHA:1561" />
        <display value="Fatal infantile cytochrome C oxidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:156140" />
        <display value="Predominantly large-vessel vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:156143" />
        <display value="Predominantly medium-vessel vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:156146" />
        <display value="Predominantly small-vessel vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:156149" />
        <display value="Immune complex mediated vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:156152" />
        <display value="Anti-neutrophil cytoplasmic antibody-associated vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:156156" />
        <display value="Lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:156159" />
        <display value="Isolated dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:1562" />
        <display value="Dacryocystitis-osteopoikilosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:156202" />
        <display value="Otomandibular dysplasia associated with monogenic syndromes" />
      </concept>
      <concept>
        <code value="ORPHA:156207" />
        <display value="Macroglossia" />
      </concept>
      <concept>
        <code value="ORPHA:156212" />
        <display value="Hypoglossia/aglossia" />
      </concept>
      <concept>
        <code value="ORPHA:156215" />
        <display value="Oromandibular-limb anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:156224" />
        <display value="Paralytic facial malformation" />
      </concept>
      <concept>
        <code value="ORPHA:156230" />
        <display value="Facial arteriovenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:156237" />
        <display value="Syndrome or malformation associated with head and neck malformations" />
      </concept>
      <concept>
        <code value="ORPHA:156243" />
        <display value="Pinnae and external auditory canal anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:156246" />
        <display value="Nose and cavum anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:156249" />
        <display value="Larynx anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:156252" />
        <display value="Tracheal anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:1563" />
        <display value="Dahlberg-Borer-Newcomer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:156532" />
        <display value="Rare syndrome with cardiac malformations" />
      </concept>
      <concept>
        <code value="ORPHA:1566" />
        <display value="Dandy-Walker malformation-postaxial polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:156601" />
        <display value="Rare genetic hepatic disease" />
      </concept>
      <concept>
        <code value="ORPHA:156604" />
        <display value="Genetic parenchymatous liver disease" />
      </concept>
      <concept>
        <code value="ORPHA:156607" />
        <display value="Genetic biliary tract disease" />
      </concept>
      <concept>
        <code value="ORPHA:156610" />
        <display value="Rare genetic respiratory disease" />
      </concept>
      <concept>
        <code value="ORPHA:156619" />
        <display value="Rare genetic urogenital disease" />
      </concept>
      <concept>
        <code value="ORPHA:156622" />
        <display value="Genetic urogenital tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:156629" />
        <display value="Genetic hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:156638" />
        <display value="Rare genetic endocrine disease" />
      </concept>
      <concept>
        <code value="ORPHA:156643" />
        <display value="Genetic endocrine growth disease" />
      </concept>
      <concept>
        <code value="ORPHA:156728" />
        <display value="Spondyloepimetaphyseal dysplasia, matrilin-3 type" />
      </concept>
      <concept>
        <code value="ORPHA:156731" />
        <display value="Dyssegmental dysplasia, Rolland-Desbuquois type" />
      </concept>
      <concept>
        <code value="ORPHA:1568" />
        <display value="X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:157" />
        <display value="Carnitine palmitoyltransferase II deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1570" />
        <display value="Symbrachydactyly of hands and feet" />
      </concept>
      <concept>
        <code value="ORPHA:1571" />
        <display value="Knobloch syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1572" />
        <display value="Common variable immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:157215" />
        <display value="Hereditary hypophosphatemic rickets with hypercalciuria" />
      </concept>
      <concept>
        <code value="ORPHA:1573" />
        <display value="Hypotrichosis with juvenile macular degeneration" />
      </concept>
      <concept>
        <code value="ORPHA:1574" />
        <display value="Retinal degeneration-nanophthalmos-glaucoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1576" />
        <display value="Infantile bilateral striatal necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:157713" />
        <display value="Congenital or early infantile CACH syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:157716" />
        <display value="Late infantile CACH syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:157719" />
        <display value="Juvenile or adult CACH syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:157769" />
        <display value="Situs ambiguus" />
      </concept>
      <concept>
        <code value="ORPHA:157791" />
        <display value="Epithelioid hemangioendothelioma" />
      </concept>
      <concept>
        <code value="ORPHA:157794" />
        <display value="Hereditary mixed polyposis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:157798" />
        <display value="Hyperplastic polyposis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1578" />
        <display value="Pterin-4 alpha-carbinolamine dehydratase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:157801" />
        <display value="Mesoaxial synostotic syndactyly with phalangeal reduction" />
      </concept>
      <concept>
        <code value="ORPHA:157808" />
        <display value="Congenital pseudoarthrosis of the limbs" />
      </concept>
      <concept>
        <code value="ORPHA:157820" />
        <display value="Cold-induced sweating syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:157823" />
        <display value="Kluver-Bucy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:157826" />
        <display value="Congenital epulis" />
      </concept>
      <concept>
        <code value="ORPHA:157832" />
        <display value="Craniorhiny" />
      </concept>
      <concept>
        <code value="ORPHA:157835" />
        <display value="Paroxysmal hemicrania" />
      </concept>
      <concept>
        <code value="ORPHA:157843" />
        <display value="Trigeminal autonomic cephalalgia" />
      </concept>
      <concept>
        <code value="ORPHA:157846" />
        <display value="Neuroferritinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:157850" />
        <display value="Pantothenate kinase-associated neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:157941" />
        <display value="Huntington disease-like 1" />
      </concept>
      <concept>
        <code value="ORPHA:157946" />
        <display value="Huntington disease-like 3" />
      </concept>
      <concept>
        <code value="ORPHA:157949" />
        <display value="Combined immunodeficiency with skin granulomas" />
      </concept>
      <concept>
        <code value="ORPHA:157954" />
        <display value="ANE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:157962" />
        <display value="Oculoauricular syndrome, Schorderet type" />
      </concept>
      <concept>
        <code value="ORPHA:157965" />
        <display value="Ehlers-Danlos syndrome, spondylocheirodysplastic type" />
      </concept>
      <concept>
        <code value="ORPHA:157973" />
        <display value="Congenital muscular dystrophy due to LMNA mutation" />
      </concept>
      <concept>
        <code value="ORPHA:157987" />
        <display value="Non-Langerhans cell histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:157991" />
        <display value="Generalized eruptive histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:157997" />
        <display value="Benign cephalic histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158" />
        <display value="Systemic primary carnitine deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1580" />
        <display value="Distal monosomy 10p" />
      </concept>
      <concept>
        <code value="ORPHA:158000" />
        <display value="Juvenile xanthogranuloma" />
      </concept>
      <concept>
        <code value="ORPHA:158003" />
        <display value="Xanthoma disseminatum" />
      </concept>
      <concept>
        <code value="ORPHA:158008" />
        <display value="Papular xanthoma" />
      </concept>
      <concept>
        <code value="ORPHA:158011" />
        <display value="Necrobiotic xanthogranuloma" />
      </concept>
      <concept>
        <code value="ORPHA:158014" />
        <display value="RosaÃ¯-Dorfman disease" />
      </concept>
      <concept>
        <code value="ORPHA:158019" />
        <display value="Indeterminate cell histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158022" />
        <display value="Progressive nodular histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158025" />
        <display value="Hereditary progressive mucinous histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158029" />
        <display value="Sea-blue histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158032" />
        <display value="Hemophagocytic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:158038" />
        <display value="Primary hemophagocytic lymphohistiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158041" />
        <display value="Secondary hemophagocytic lymphohistiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158048" />
        <display value="Hemophagocytic syndrome associated with an infection" />
      </concept>
      <concept>
        <code value="ORPHA:158057" />
        <display value="Acquired hemophagocytic lymphohistiocytosis associated with malignant disease" />
      </concept>
      <concept>
        <code value="ORPHA:158061" />
        <display value="Macrophage activation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1581" />
        <display value="Non-distal monosomy 10q" />
      </concept>
      <concept>
        <code value="ORPHA:158124" />
        <display value="Genetic dementia" />
      </concept>
      <concept>
        <code value="ORPHA:158266" />
        <display value="Huntington disease-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:158300" />
        <display value="Rare genetic hematologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:158661" />
        <display value="Suprabasal epidermolysis bullosa simplex" />
      </concept>
      <concept>
        <code value="ORPHA:158665" />
        <display value="Basal epidermolysis bullosa simplex" />
      </concept>
      <concept>
        <code value="ORPHA:158668" />
        <display value="Epidermolysis bullosa simplex due to plakophilin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:158673" />
        <display value="Acral dystrophic epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:158676" />
        <display value="Dominant dystrophic epidermolysis bullosa, nails only" />
      </concept>
      <concept>
        <code value="ORPHA:158681" />
        <display value="Epidermolysis bullosa simplex with circinate migratory erythema" />
      </concept>
      <concept>
        <code value="ORPHA:158684" />
        <display value="Epidermolysis bullosa simplex with pyloric atresia" />
      </concept>
      <concept>
        <code value="ORPHA:158687" />
        <display value="Lethal acantholytic epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:1587" />
        <display value="Monosomy 13q14" />
      </concept>
      <concept>
        <code value="ORPHA:158766" />
        <display value="Typical urticaria pigmentosa" />
      </concept>
      <concept>
        <code value="ORPHA:158769" />
        <display value="Plaque-form urticaria pigmentosa" />
      </concept>
      <concept>
        <code value="ORPHA:158772" />
        <display value="Nodular urticaria pigmentosa" />
      </concept>
      <concept>
        <code value="ORPHA:158775" />
        <display value="Smouldering systemic mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158778" />
        <display value="Isolated bone marrow mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:158793" />
        <display value="Lymphoadenopathic mastocytosis with eosinophilia" />
      </concept>
      <concept>
        <code value="ORPHA:158796" />
        <display value="Classic mast cell leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:158799" />
        <display value="Aleukemic mast cell leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:159" />
        <display value="Carnitine-acylcarnitine translocase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1590" />
        <display value="Distal monosomy 13q" />
      </concept>
      <concept>
        <code value="ORPHA:1596" />
        <display value="Distal monosomy 15q" />
      </concept>
      <concept>
        <code value="ORPHA:1597" />
        <display value="Distal monosomy 17q" />
      </concept>
      <concept>
        <code value="ORPHA:1598" />
        <display value="Monosomy 18p" />
      </concept>
      <concept>
        <code value="ORPHA:16" />
        <display value="Blue cone monochromatism" />
      </concept>
      <concept>
        <code value="ORPHA:160" />
        <display value="Castleman disease" />
      </concept>
      <concept>
        <code value="ORPHA:1600" />
        <display value="Monosomy 18q" />
      </concept>
      <concept>
        <code value="ORPHA:160148" />
        <display value="Cap polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:1606" />
        <display value="1p36 deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1617" />
        <display value="2q24 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:162" />
        <display value="Cataract-glaucoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1620" />
        <display value="Distal monosomy 3p" />
      </concept>
      <concept>
        <code value="ORPHA:1621" />
        <display value="3q13 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:162516" />
        <display value="Isolated congenital nasal pyriform aperture stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:162526" />
        <display value="Isolated congenital auditory ossicle malformation" />
      </concept>
      <concept>
        <code value="ORPHA:1627" />
        <display value="Deletion 5q35" />
      </concept>
      <concept>
        <code value="ORPHA:163" />
        <display value="Hereditary hyperferritinemia-cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163209" />
        <display value="Non-syndromic cerebral malformation due to abnormal neuronal migration" />
      </concept>
      <concept>
        <code value="ORPHA:163525" />
        <display value="Subacute cutaneous lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:163531" />
        <display value="Chronic cutaneous lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:163582" />
        <display value="Rare bacterial infectious disease" />
      </concept>
      <concept>
        <code value="ORPHA:163585" />
        <display value="Rare viral disease" />
      </concept>
      <concept>
        <code value="ORPHA:163588" />
        <display value="Rare parasitic disease" />
      </concept>
      <concept>
        <code value="ORPHA:163591" />
        <display value="Rare mycosis" />
      </concept>
      <concept>
        <code value="ORPHA:163596" />
        <display value="Hb Barts hydrops fetalis" />
      </concept>
      <concept>
        <code value="ORPHA:1636" />
        <display value="Distal monosomy 7q36" />
      </concept>
      <concept>
        <code value="ORPHA:163631" />
        <display value="Bile acid synthesis defect with cholestasis and malabsorption" />
      </concept>
      <concept>
        <code value="ORPHA:163634" />
        <display value="Maffucci syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163637" />
        <display value="Rare disorder related with pregnancy, childbirth and puerperium" />
      </concept>
      <concept>
        <code value="ORPHA:163649" />
        <display value="Spondyloepiphyseal dysplasia, Nishimura type" />
      </concept>
      <concept>
        <code value="ORPHA:163654" />
        <display value="Spondyloepiphyseal dysplasia, Cantu type" />
      </concept>
      <concept>
        <code value="ORPHA:163662" />
        <display value="Spondyloepiphyseal dysplasia, Reardon type" />
      </concept>
      <concept>
        <code value="ORPHA:163665" />
        <display value="Spondyloepiphyseal dysplasia tarda, Kohn type" />
      </concept>
      <concept>
        <code value="ORPHA:163668" />
        <display value="Spondyloepiphyseal dysplasia, MacDermot type" />
      </concept>
      <concept>
        <code value="ORPHA:163681" />
        <display value="Cortical dysplasia-focal epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163684" />
        <display value="Leukoencephalopathy-dystonia-motor neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163690" />
        <display value="Hypotonia-cystinuria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163693" />
        <display value="2p21 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163696" />
        <display value="Action myoclonus-renal failure syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163699" />
        <display value="Alveolar soft tissue sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:163703" />
        <display value="Febrile infection-related epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163708" />
        <display value="Cryptogenic late-onset epileptic spasms" />
      </concept>
      <concept>
        <code value="ORPHA:163717" />
        <display value="Benign familial mesial temporal lobe epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:163721" />
        <display value="Rolandic epilepsy-speech dyspraxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163727" />
        <display value="Rolandic epilepsy-paroxysmal exercise-induced dystonia-writers cramp syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163746" />
        <display value="Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease" />
      </concept>
      <concept>
        <code value="ORPHA:163892" />
        <display value="Limbic encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:163895" />
        <display value="Paraneoplastic limbic encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:163898" />
        <display value="Classic paraneoplastic limbic encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:163903" />
        <display value="Limbic encephalitis associated with antibodies to cell membrane antigens" />
      </concept>
      <concept>
        <code value="ORPHA:163908" />
        <display value="Limbic encephalitis with LGI1 antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:163918" />
        <display value="Non-paraneoplastic limbic encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:163921" />
        <display value="Posttransplant acute limbic encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:163924" />
        <display value="Non-herpetic acute limbic encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:163927" />
        <display value="Pustulosis palmaris et plantaris" />
      </concept>
      <concept>
        <code value="ORPHA:163931" />
        <display value="Acrodermatitis continua of Hallopeau" />
      </concept>
      <concept>
        <code value="ORPHA:163934" />
        <display value="Atopic keratoconjunctivitis" />
      </concept>
      <concept>
        <code value="ORPHA:163937" />
        <display value="X-linked intellectual disability, Najm type" />
      </concept>
      <concept>
        <code value="ORPHA:163956" />
        <display value="X-linked intellectual disability, Nascimento type" />
      </concept>
      <concept>
        <code value="ORPHA:163961" />
        <display value="X-linked cerebral-cerebellar-coloboma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163966" />
        <display value="X-linked dominant chondrodysplasia, Chassaing-Lacombe type" />
      </concept>
      <concept>
        <code value="ORPHA:163971" />
        <display value="X-linked intellectual disability, Cilliers type" />
      </concept>
      <concept>
        <code value="ORPHA:163976" />
        <display value="X-linked intellectual disability, Van Esch type" />
      </concept>
      <concept>
        <code value="ORPHA:163979" />
        <display value="X-linked intellectual disability-craniofacioskeletal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163985" />
        <display value="Hyperekplexia-epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:163988" />
        <display value="Developmental delay-deafness syndrome, Hildebrand type" />
      </concept>
      <concept>
        <code value="ORPHA:164001" />
        <display value="Rare odontal or periodontal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:164004" />
        <display value="Middle ear anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:1642" />
        <display value="Distal monosomy 9p" />
      </concept>
      <concept>
        <code value="ORPHA:1643" />
        <display value="Xp22.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1646" />
        <display value="Partial chromosome Y deletion" />
      </concept>
      <concept>
        <code value="ORPHA:1647" />
        <display value="Oculocerebrocutaneous syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:164726" />
        <display value="Acute myeloid leukemia and myelodysplastic syndromes related to radiation" />
      </concept>
      <concept>
        <code value="ORPHA:164736" />
        <display value="Familial advanced sleep-phase syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:164823" />
        <display value="Rare acquired aplastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:165" />
        <display value="Neutral lipid storage disease" />
      </concept>
      <concept>
        <code value="ORPHA:1652" />
        <display value="Dent disease" />
      </concept>
      <concept>
        <code value="ORPHA:1653" />
        <display value="Dentin dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1655" />
        <display value="Mullerian derivatives-lymphangiectasia-polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1656" />
        <display value="Dermatitis herpetiformis" />
      </concept>
      <concept>
        <code value="ORPHA:165652" />
        <display value="Rare genetic gastroenterological disease" />
      </concept>
      <concept>
        <code value="ORPHA:165655" />
        <display value="Genetic intestinal disease" />
      </concept>
      <concept>
        <code value="ORPHA:165658" />
        <display value="Genetic gastro-esophageal disease" />
      </concept>
      <concept>
        <code value="ORPHA:165661" />
        <display value="Genetic pancreatic disease" />
      </concept>
      <concept>
        <code value="ORPHA:1657" />
        <display value="Dermatoosteolysis, Kirghizian type" />
      </concept>
      <concept>
        <code value="ORPHA:165704" />
        <display value="Non-syndromic urogenital tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:165707" />
        <display value="Syndromic urogenital tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:165711" />
        <display value="Rare abdominal surgical disease" />
      </concept>
      <concept>
        <code value="ORPHA:1658" />
        <display value="Absence of fingerprints-congenital milia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:165805" />
        <display value="Familial mesial temporal lobe epilepsy with febrile seizures" />
      </concept>
      <concept>
        <code value="ORPHA:1659" />
        <display value="Dermatoleukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:165955" />
        <display value="Wound myiasis" />
      </concept>
      <concept>
        <code value="ORPHA:165958" />
        <display value="Cavitary myiasis" />
      </concept>
      <concept>
        <code value="ORPHA:165985" />
        <display value="Diazoxide-sensitive diffuse hyperinsulinism" />
      </concept>
      <concept>
        <code value="ORPHA:165988" />
        <display value="Diazoxide-resistant diffuse hyperinsulinism" />
      </concept>
      <concept>
        <code value="ORPHA:165991" />
        <display value="Exercise-induced hyperinsulinism" />
      </concept>
      <concept>
        <code value="ORPHA:165994" />
        <display value="Pituitary resistance to thyroid hormone" />
      </concept>
      <concept>
        <code value="ORPHA:166" />
        <display value="Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:1660" />
        <display value="Dermoodontodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:166002" />
        <display value="Multiple epiphyseal dysplasia due to collagen 9 anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:166011" />
        <display value="Multiple epiphyseal dysplasia, Beighton type" />
      </concept>
      <concept>
        <code value="ORPHA:166016" />
        <display value="Multiple epiphyseal dysplasia, Lowry type" />
      </concept>
      <concept>
        <code value="ORPHA:166024" />
        <display value="Multiple epiphyseal dysplasia, Al-Gazali type" />
      </concept>
      <concept>
        <code value="ORPHA:166029" />
        <display value="Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:166032" />
        <display value="Multiple epiphyseal dysplasia, with miniepiphyses" />
      </concept>
      <concept>
        <code value="ORPHA:166035" />
        <display value="Brachydactyly-short stature-retinitis pigmentosa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:166038" />
        <display value="Metaphyseal chondrodysplasia, Kaitila type" />
      </concept>
      <concept>
        <code value="ORPHA:166063" />
        <display value="Pontocerebellar hypoplasia type 4" />
      </concept>
      <concept>
        <code value="ORPHA:166068" />
        <display value="Pontocerebellar hypoplasia type 5" />
      </concept>
      <concept>
        <code value="ORPHA:166073" />
        <display value="Pontocerebellar hypoplasia type 6" />
      </concept>
      <concept>
        <code value="ORPHA:166078" />
        <display value="Von Willebrand disease type 1" />
      </concept>
      <concept>
        <code value="ORPHA:166081" />
        <display value="Von Willebrand disease type 2" />
      </concept>
      <concept>
        <code value="ORPHA:166084" />
        <display value="Von Willebrand disease type 2A" />
      </concept>
      <concept>
        <code value="ORPHA:166087" />
        <display value="Von Willebrand disease type 2B" />
      </concept>
      <concept>
        <code value="ORPHA:166090" />
        <display value="Von Willebrand disease type 2M" />
      </concept>
      <concept>
        <code value="ORPHA:166093" />
        <display value="Von Willebrand disease type 2N" />
      </concept>
      <concept>
        <code value="ORPHA:166096" />
        <display value="Von Willebrand disease type 3" />
      </concept>
      <concept>
        <code value="ORPHA:1661" />
        <display value="X-linked corneal dermoid" />
      </concept>
      <concept>
        <code value="ORPHA:166100" />
        <display value="Stickler syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:166105" />
        <display value="FASTKD2-related infantile mitochondrial encephalomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:166108" />
        <display value="Intellectual disability, Birk-Barel type" />
      </concept>
      <concept>
        <code value="ORPHA:166113" />
        <display value="Bazex syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:166119" />
        <display value="Isolated osteopoikilosis" />
      </concept>
      <concept>
        <code value="ORPHA:1662" />
        <display value="Restrictive dermopathy" />
      </concept>
      <concept>
        <code value="ORPHA:166260" />
        <display value="Dentinogenesis imperfecta type 2" />
      </concept>
      <concept>
        <code value="ORPHA:166265" />
        <display value="Dentinogenesis imperfecta type 3" />
      </concept>
      <concept>
        <code value="ORPHA:166272" />
        <display value="Odontochondrodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:166277" />
        <display value="Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:166282" />
        <display value="Familial sick sinus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:166286" />
        <display value="Porokeratotic eccrine ostial and dermal duct nevus" />
      </concept>
      <concept>
        <code value="ORPHA:166291" />
        <display value="Dirofilariasis" />
      </concept>
      <concept>
        <code value="ORPHA:166295" />
        <display value="Benign non-familial infantile seizures" />
      </concept>
      <concept>
        <code value="ORPHA:166299" />
        <display value="Benign partial epilepsy of infancy with complex partial seizures" />
      </concept>
      <concept>
        <code value="ORPHA:166302" />
        <display value="Benign partial epilepsy with secondarily generalized seizures in infancy" />
      </concept>
      <concept>
        <code value="ORPHA:166305" />
        <display value="Benign infantile seizures associated with mild gastroenteritis" />
      </concept>
      <concept>
        <code value="ORPHA:166308" />
        <display value="Benign infantile focal epilepsy with midline spikes and waves during sleep" />
      </concept>
      <concept>
        <code value="ORPHA:166311" />
        <display value="Benign partial infantile seizures" />
      </concept>
      <concept>
        <code value="ORPHA:166409" />
        <display value="Photosensitive epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166412" />
        <display value="Hot water reflex epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166415" />
        <display value="Audiogenic seizures" />
      </concept>
      <concept>
        <code value="ORPHA:166418" />
        <display value="Eating reflex epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166421" />
        <display value="Orgasm-induced seizures" />
      </concept>
      <concept>
        <code value="ORPHA:166424" />
        <display value="Thinking seizures" />
      </concept>
      <concept>
        <code value="ORPHA:166427" />
        <display value="Startle epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166430" />
        <display value="Micturation-induced seizures" />
      </concept>
      <concept>
        <code value="ORPHA:166433" />
        <display value="Reading seizures" />
      </concept>
      <concept>
        <code value="ORPHA:166463" />
        <display value="Epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:166466" />
        <display value="Neurocutaneous syndrome with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166469" />
        <display value="Chromosomal anomaly with epilepsy as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:166472" />
        <display value="Monogenic disease with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166475" />
        <display value="Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes" />
      </concept>
      <concept>
        <code value="ORPHA:166478" />
        <display value="Cerebral malformation with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166481" />
        <display value="Metabolic diseases with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166484" />
        <display value="Inflammatory and autoimmune disease with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166487" />
        <display value="Cerebral diseases of vascular origin with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:166490" />
        <display value="Infectious disease with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:1665" />
        <display value="Sporadic fetal brain disruption sequence" />
      </concept>
      <concept>
        <code value="ORPHA:1666" />
        <display value="Dextrocardia" />
      </concept>
      <concept>
        <code value="ORPHA:1667" />
        <display value="Wolcott-Rallison syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:166775" />
        <display value="Rare hemorrhagic disorder due to an acquired coagulation factor defect" />
      </concept>
      <concept>
        <code value="ORPHA:167" />
        <display value="Chediak-Higashi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1670" />
        <display value="Chronic diarrhea with villous atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1671" />
        <display value="Diastematomyelia" />
      </concept>
      <concept>
        <code value="ORPHA:1672" />
        <display value="Diencephalic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1675" />
        <display value="Dihydropyrimidine dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1676" />
        <display value="Idiopathic pulmonary artery dilatation" />
      </concept>
      <concept>
        <code value="ORPHA:167635" />
        <display value="Scleromyxedema" />
      </concept>
      <concept>
        <code value="ORPHA:1677" />
        <display value="Familial idiopathic dilatation of the right atrium" />
      </concept>
      <concept>
        <code value="ORPHA:167714" />
        <display value="Unclassified acute myeloid leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:167759" />
        <display value="Hereditary dentin defect" />
      </concept>
      <concept>
        <code value="ORPHA:167762" />
        <display value="Rare disease with dentinogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:167848" />
        <display value="Cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1679" />
        <display value="Diphtheria" />
      </concept>
      <concept>
        <code value="ORPHA:168" />
        <display value="Loose anagen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1681" />
        <display value="Diprosopus" />
      </concept>
      <concept>
        <code value="ORPHA:168194" />
        <display value="Rare cardiac tumor" />
      </concept>
      <concept>
        <code value="ORPHA:1682" />
        <display value="Arterial dissection-lentiginosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168443" />
        <display value="Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168448" />
        <display value="Spondyloepimetaphyseal dysplasia, Bieganski type" />
      </concept>
      <concept>
        <code value="ORPHA:168451" />
        <display value="Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168454" />
        <display value="Spondyloepimetaphyseal dysplasia, Geneviave type" />
      </concept>
      <concept>
        <code value="ORPHA:168486" />
        <display value="Congenital neuronal ceroid lipofuscinosis" />
      </concept>
      <concept>
        <code value="ORPHA:168491" />
        <display value="Late infantile neuronal ceroid lipofuscinosis" />
      </concept>
      <concept>
        <code value="ORPHA:1685" />
        <display value="Distomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:168544" />
        <display value="Spondylometaphyseal dysplasia, Golden type" />
      </concept>
      <concept>
        <code value="ORPHA:168549" />
        <display value="Axial spondylometaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:168552" />
        <display value="Spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168555" />
        <display value="Spondylometaphyseal dysplasia, A4 type" />
      </concept>
      <concept>
        <code value="ORPHA:168558" />
        <display value="46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:168563" />
        <display value="46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168566" />
        <display value="Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3" />
      </concept>
      <concept>
        <code value="ORPHA:168569" />
        <display value="H syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168572" />
        <display value="Native American myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:168577" />
        <display value="Hereditary cryohydrocytosis with reduced stomatin" />
      </concept>
      <concept>
        <code value="ORPHA:168583" />
        <display value="Hereditary North American Indian childhood cirrhosis" />
      </concept>
      <concept>
        <code value="ORPHA:168588" />
        <display value="Hyperandrogenism due to cortisone reductase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:168593" />
        <display value="Sudden infant death-dysgenesis of the testes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168598" />
        <display value="Brain demyelination due to methionine adenosyltransferase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1686" />
        <display value="Cardiac diverticulum" />
      </concept>
      <concept>
        <code value="ORPHA:168601" />
        <display value="Congenital enteropathy due to enteropeptidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:168606" />
        <display value="Seborrhea-like dermatitis with psoriasiform elements" />
      </concept>
      <concept>
        <code value="ORPHA:168609" />
        <display value="Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure" />
      </concept>
      <concept>
        <code value="ORPHA:168612" />
        <display value="Congenital deficiency in alpha-fetoprotein" />
      </concept>
      <concept>
        <code value="ORPHA:168615" />
        <display value="Hereditary persistence of alpha-fetoprotein" />
      </concept>
      <concept>
        <code value="ORPHA:168621" />
        <display value="Dysplasia of head of femur, Meyer type" />
      </concept>
      <concept>
        <code value="ORPHA:168624" />
        <display value="Familial scaphocephaly syndrome, McGillivray type" />
      </concept>
      <concept>
        <code value="ORPHA:168629" />
        <display value="Autosomal thrombocytopenia with normal platelets" />
      </concept>
      <concept>
        <code value="ORPHA:168632" />
        <display value="Generalized basaloid follicular hamartoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168778" />
        <display value="Rare pervasive developmental disorder" />
      </concept>
      <concept>
        <code value="ORPHA:168782" />
        <display value="Childhood disintegrative disorder" />
      </concept>
      <concept>
        <code value="ORPHA:168796" />
        <display value="Heart-hand syndrome, Slovenian type" />
      </concept>
      <concept>
        <code value="ORPHA:168803" />
        <display value="Primary peritoneal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:168807" />
        <display value="Primary malignant peritoneal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:168811" />
        <display value="Malignant peritoneal mesothelioma" />
      </concept>
      <concept>
        <code value="ORPHA:168816" />
        <display value="Peritoneal cystic mesothelioma" />
      </concept>
      <concept>
        <code value="ORPHA:168829" />
        <display value="Primary peritoneal carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:168940" />
        <display value="Chronic eosinophilic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:168943" />
        <display value="Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1" />
      </concept>
      <concept>
        <code value="ORPHA:168947" />
        <display value="Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement" />
      </concept>
      <concept>
        <code value="ORPHA:168950" />
        <display value="Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement" />
      </concept>
      <concept>
        <code value="ORPHA:168953" />
        <display value="Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement" />
      </concept>
      <concept>
        <code value="ORPHA:168956" />
        <display value="Hypereosinophilic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168960" />
        <display value="Refractory anemia with excess blasts in transformation" />
      </concept>
      <concept>
        <code value="ORPHA:168966" />
        <display value="Composite lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:168984" />
        <display value="CLAPO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:168999" />
        <display value="Malignant melanoma of the mucosa" />
      </concept>
      <concept>
        <code value="ORPHA:169" />
        <display value="Ringed hair disease" />
      </concept>
      <concept>
        <code value="ORPHA:169079" />
        <display value="Cernunnos-XLF deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169082" />
        <display value="Combined immunodeficiency due to CD3gamma deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169085" />
        <display value="Susceptibility to respiratory infections associated with CD8alpha chain mutation" />
      </concept>
      <concept>
        <code value="ORPHA:169090" />
        <display value="Combined immunodeficiency due to CRAC channel dysfunction" />
      </concept>
      <concept>
        <code value="ORPHA:169095" />
        <display value="Alymphoid cystic thymic dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:169100" />
        <display value="Immunodeficiency due to CD25 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169105" />
        <display value="Good syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:169110" />
        <display value="Immunoglobulin heavy chain deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169139" />
        <display value="Transient hypogammaglobulinemia of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:169142" />
        <display value="Recurrent infection due to specific granule deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169147" />
        <display value="Immunodeficiency due to a classical component pathway complement deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169150" />
        <display value="Immunodeficiency due to a late component of complement deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169154" />
        <display value="T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169157" />
        <display value="T-B+ severe combined immunodeficiency due to CD45 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169160" />
        <display value="T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta" />
      </concept>
      <concept>
        <code value="ORPHA:169163" />
        <display value="Familial scaphocephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:169186" />
        <display value="Autosomal recessive centronuclear myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:169189" />
        <display value="Autosomal dominant centronuclear myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1692" />
        <display value="Mosaic trisomy 1" />
      </concept>
      <concept>
        <code value="ORPHA:169346" />
        <display value="DNA repair defect other than combined T-cell and B-cell immunodeficiencies" />
      </concept>
      <concept>
        <code value="ORPHA:169349" />
        <display value="Immuno-osseous dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:169355" />
        <display value="Immunodeficiency syndrome with autoimmunity" />
      </concept>
      <concept>
        <code value="ORPHA:169361" />
        <display value="Immune dysregulation disease with immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169443" />
        <display value="Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells" />
      </concept>
      <concept>
        <code value="ORPHA:169464" />
        <display value="Primary CD59 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:169467" />
        <display value="Recurrent Neisseria infections due to factor D deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1695" />
        <display value="Non-distal trisomy 10q" />
      </concept>
      <concept>
        <code value="ORPHA:169615" />
        <display value="Idiopathic central precocious puberty" />
      </concept>
      <concept>
        <code value="ORPHA:169618" />
        <display value="Secondary central precocious puberty" />
      </concept>
      <concept>
        <code value="ORPHA:169793" />
        <display value="Severe hemophilia B" />
      </concept>
      <concept>
        <code value="ORPHA:169796" />
        <display value="Moderately severe hemophilia B" />
      </concept>
      <concept>
        <code value="ORPHA:169799" />
        <display value="Mild hemophilia B" />
      </concept>
      <concept>
        <code value="ORPHA:1698" />
        <display value="Mosaic trisomy 12" />
      </concept>
      <concept>
        <code value="ORPHA:169802" />
        <display value="Severe hemophilia A" />
      </concept>
      <concept>
        <code value="ORPHA:169805" />
        <display value="Moderately severe hemophilia A" />
      </concept>
      <concept>
        <code value="ORPHA:169808" />
        <display value="Mild hemophilia A" />
      </concept>
      <concept>
        <code value="ORPHA:169826" />
        <display value="Congenital vitamin K-dependent coagulation factors deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1699" />
        <display value="Trisomy 12p" />
      </concept>
      <concept>
        <code value="ORPHA:17" />
        <display value="Fatal infantile lactic acidosis with methylmalonic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:170" />
        <display value="Woolly hair" />
      </concept>
      <concept>
        <code value="ORPHA:1702" />
        <display value="Non-distal trisomy 13q" />
      </concept>
      <concept>
        <code value="ORPHA:1703" />
        <display value="Mosaic trisomy 14" />
      </concept>
      <concept>
        <code value="ORPHA:1705" />
        <display value="Distal trisomy 14q" />
      </concept>
      <concept>
        <code value="ORPHA:1706" />
        <display value="Mosaic trisomy 15" />
      </concept>
      <concept>
        <code value="ORPHA:1707" />
        <display value="Distal trisomy 15q" />
      </concept>
      <concept>
        <code value="ORPHA:1708" />
        <display value="Mosaic trisomy 16" />
      </concept>
      <concept>
        <code value="ORPHA:171" />
        <display value="Primary sclerosing cholangitis" />
      </concept>
      <concept>
        <code value="ORPHA:1711" />
        <display value="Mosaic trisomy 17" />
      </concept>
      <concept>
        <code value="ORPHA:171201" />
        <display value="High anorectal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:171208" />
        <display value="Intermediate anorectal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:171215" />
        <display value="Low anorectal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:171220" />
        <display value="Rectal duplication" />
      </concept>
      <concept>
        <code value="ORPHA:1713" />
        <display value="17p11.2 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171430" />
        <display value="Severe congenital nemaline myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171433" />
        <display value="Intermediate nemaline myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171436" />
        <display value="Typical nemaline myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171439" />
        <display value="Childhood-onset nemaline myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171442" />
        <display value="Adult-onset nemaline myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171445" />
        <display value="Muscle filaminopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1715" />
        <display value="Trisomy 18p" />
      </concept>
      <concept>
        <code value="ORPHA:1716" />
        <display value="Distal trisomy 18q" />
      </concept>
      <concept>
        <code value="ORPHA:171607" />
        <display value="X-linked spastic paraplegia type 34" />
      </concept>
      <concept>
        <code value="ORPHA:171612" />
        <display value="Autosomal dominant spastic paraplegia type 37" />
      </concept>
      <concept>
        <code value="ORPHA:171617" />
        <display value="Autosomal dominant spastic paraplegia type 38" />
      </concept>
      <concept>
        <code value="ORPHA:171622" />
        <display value="Autosomal recessive spastic paraplegia type 32" />
      </concept>
      <concept>
        <code value="ORPHA:171629" />
        <display value="Autosomal recessive spastic paraplegia type 35" />
      </concept>
      <concept>
        <code value="ORPHA:171680" />
        <display value="Lissencephaly due to TUBA1A mutation" />
      </concept>
      <concept>
        <code value="ORPHA:171684" />
        <display value="Idiopathic bilateral vestibulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171690" />
        <display value="Metabolic myopathy due to lactate transporter defect" />
      </concept>
      <concept>
        <code value="ORPHA:171695" />
        <display value="Parkinsonian-pyramidal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1717" />
        <display value="Distal trisomy 19q" />
      </concept>
      <concept>
        <code value="ORPHA:171700" />
        <display value="Diffuse panbronchiolitis" />
      </concept>
      <concept>
        <code value="ORPHA:171703" />
        <display value="Microcephaly-polymicrogyria-corpus callosum agenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171706" />
        <display value="Short stature-delayed bone age due to thyroid hormone metabolism deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:171709" />
        <display value="Male infertility due to globozoospermia" />
      </concept>
      <concept>
        <code value="ORPHA:171714" />
        <display value="Amish infantile epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171719" />
        <display value="Cutis laxa-Marfanoid syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171723" />
        <display value="White sponge nevus" />
      </concept>
      <concept>
        <code value="ORPHA:171829" />
        <display value="6q16 deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171839" />
        <display value="Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171844" />
        <display value="Blindness-scoliosis-arachnodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171848" />
        <display value="Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171851" />
        <display value="MEDNIK syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171860" />
        <display value="Intellectual disability-cataracts-kyphosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:171863" />
        <display value="Autosomal dominant spastic paraplegia type 42" />
      </concept>
      <concept>
        <code value="ORPHA:171866" />
        <display value="Spondyloepimetaphyseal dysplasia, aggrecan type" />
      </concept>
      <concept>
        <code value="ORPHA:171871" />
        <display value="Renal pseudohypoaldosteronism type 1" />
      </concept>
      <concept>
        <code value="ORPHA:171876" />
        <display value="Generalized pseudohypoaldosteronism type 1" />
      </concept>
      <concept>
        <code value="ORPHA:171881" />
        <display value="Cap myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171886" />
        <display value="Cylindrical spirals myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171889" />
        <display value="Myopathy with hexagonally cross-linked tubular arrays" />
      </concept>
      <concept>
        <code value="ORPHA:171895" />
        <display value="Myeloid hemopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171898" />
        <display value="Lymphoid hemopathy" />
      </concept>
      <concept>
        <code value="ORPHA:171901" />
        <display value="Primary cutaneous T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:171915" />
        <display value="B-cell non-Hodgkin lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:171918" />
        <display value="T-cell non-Hodgkin lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:171929" />
        <display value="Trisomy 10p" />
      </concept>
      <concept>
        <code value="ORPHA:172" />
        <display value="Progressive familial intrahepatic cholestasis" />
      </concept>
      <concept>
        <code value="ORPHA:1723" />
        <display value="Mosaic trisomy 2" />
      </concept>
      <concept>
        <code value="ORPHA:1724" />
        <display value="Mosaic trisomy 20" />
      </concept>
      <concept>
        <code value="ORPHA:1727" />
        <display value="22q11.2 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:172976" />
        <display value="Congenital myopathy with cores" />
      </concept>
      <concept>
        <code value="ORPHA:173" />
        <display value="Cholera" />
      </concept>
      <concept>
        <code value="ORPHA:1738" />
        <display value="Trisomy 4p" />
      </concept>
      <concept>
        <code value="ORPHA:174" />
        <display value="Metaphyseal chondrodysplasia, Schmid type" />
      </concept>
      <concept>
        <code value="ORPHA:1742" />
        <display value="Trisomy 5p" />
      </concept>
      <concept>
        <code value="ORPHA:1745" />
        <display value="Distal trisomy 6p" />
      </concept>
      <concept>
        <code value="ORPHA:174590" />
        <display value="Congenital hypogonadotropic hypogonadism" />
      </concept>
      <concept>
        <code value="ORPHA:1747" />
        <display value="Mosaic trisomy 7" />
      </concept>
      <concept>
        <code value="ORPHA:175" />
        <display value="Cartilage-hair hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1752" />
        <display value="Trisomy 8q" />
      </concept>
      <concept>
        <code value="ORPHA:1756" />
        <display value="Caudal duplication" />
      </concept>
      <concept>
        <code value="ORPHA:1757" />
        <display value="Fibular dimelia-diplopodia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1759" />
        <display value="Thoraco-abdominal enteric duplication" />
      </concept>
      <concept>
        <code value="ORPHA:176" />
        <display value="Non-rhizomelic chondrodysplasia punctata" />
      </concept>
      <concept>
        <code value="ORPHA:1762" />
        <display value="Trisomy Xq28" />
      </concept>
      <concept>
        <code value="ORPHA:1764" />
        <display value="Familial dysautonomia" />
      </concept>
      <concept>
        <code value="ORPHA:1765" />
        <display value="Dyschondrosteosis-nephritis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1766" />
        <display value="Dysequilibrium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1768" />
        <display value="Familial caudal dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:177" />
        <display value="Rhizomelic chondrodysplasia punctata" />
      </concept>
      <concept>
        <code value="ORPHA:1770" />
        <display value="XY type gonadal dysgenesis-associated anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:177101" />
        <display value="Rare adult hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:177107" />
        <display value="Syndromic hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:1772" />
        <display value="45,X/46,XY mixed gonadal dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:1775" />
        <display value="Dyskeratosis congenita" />
      </concept>
      <concept>
        <code value="ORPHA:1777" />
        <display value="Temtamy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1778" />
        <display value="Facial dysmorphism-shawl scrotum-joint laxity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1779" />
        <display value="Dysmorphism-cleft palate-loose skin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:177901" />
        <display value="Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1" />
      </concept>
      <concept>
        <code value="ORPHA:177904" />
        <display value="Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2" />
      </concept>
      <concept>
        <code value="ORPHA:177907" />
        <display value="Prader-Willi syndrome due to translocation" />
      </concept>
      <concept>
        <code value="ORPHA:177910" />
        <display value="Prader-Willi syndrome due to imprinting mutation" />
      </concept>
      <concept>
        <code value="ORPHA:177926" />
        <display value="Symptomatic form of hemophilia A in female carriers" />
      </concept>
      <concept>
        <code value="ORPHA:177929" />
        <display value="Symptomatic form of hemophilia B in female carriers" />
      </concept>
      <concept>
        <code value="ORPHA:178" />
        <display value="Chordoma" />
      </concept>
      <concept>
        <code value="ORPHA:1780" />
        <display value="Thakker-Donnai syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:178025" />
        <display value="Non-acquired combined pituitary hormone deficiencies without extra-pituitary malformations" />
      </concept>
      <concept>
        <code value="ORPHA:178029" />
        <display value="Central diabetes insipidus" />
      </concept>
      <concept>
        <code value="ORPHA:178040" />
        <display value="Peripheral precocious puberty" />
      </concept>
      <concept>
        <code value="ORPHA:178045" />
        <display value="Transient congenital hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:178145" />
        <display value="Moderate multiminicore disease with hand involvement" />
      </concept>
      <concept>
        <code value="ORPHA:178148" />
        <display value="Antenatal multiminicore disease with arthrogryposis multiplex congenita" />
      </concept>
      <concept>
        <code value="ORPHA:1782" />
        <display value="Dysosteosclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:178303" />
        <display value="8q22.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:178307" />
        <display value="Reticulate acropigmentation of Kitamura" />
      </concept>
      <concept>
        <code value="ORPHA:178311" />
        <display value="Isolated sternocostoclavicular hyperostosis" />
      </concept>
      <concept>
        <code value="ORPHA:178315" />
        <display value="Undifferentiated embryonal sarcoma of the liver" />
      </concept>
      <concept>
        <code value="ORPHA:178320" />
        <display value="Acute lung injury" />
      </concept>
      <concept>
        <code value="ORPHA:178330" />
        <display value="Heinz body anemia" />
      </concept>
      <concept>
        <code value="ORPHA:178333" />
        <display value="Aland Islands eye disease" />
      </concept>
      <concept>
        <code value="ORPHA:178338" />
        <display value="UV-sensitive syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:178342" />
        <display value="Inflammatory myofibroblastic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:178345" />
        <display value="Aromatase excess syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:178355" />
        <display value="Smith-McCort dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:178364" />
        <display value="Syndromic microphthalmia type 5" />
      </concept>
      <concept>
        <code value="ORPHA:178377" />
        <display value="Osteosclerosis-developmental delay-craniosynostosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:178382" />
        <display value="Congenital vertical talus" />
      </concept>
      <concept>
        <code value="ORPHA:178389" />
        <display value="Osteopetrosis-hypogammaglobulinemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:178396" />
        <display value="Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation" />
      </concept>
      <concept>
        <code value="ORPHA:1784" />
        <display value="Acrofrontofacionasal dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:178400" />
        <display value="Distal myopathy with anterior tibial onset" />
      </concept>
      <concept>
        <code value="ORPHA:178461" />
        <display value="X-linked myopathy with postural muscle atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:178464" />
        <display value="Hereditary proximal myopathy with early respiratory failure" />
      </concept>
      <concept>
        <code value="ORPHA:178469" />
        <display value="Autosomal dominant non-syndromic intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:178475" />
        <display value="Wound botulism" />
      </concept>
      <concept>
        <code value="ORPHA:178478" />
        <display value="Infant botulism" />
      </concept>
      <concept>
        <code value="ORPHA:178481" />
        <display value="Intestinal botulism" />
      </concept>
      <concept>
        <code value="ORPHA:178487" />
        <display value="Adult intestinal botulism" />
      </concept>
      <concept>
        <code value="ORPHA:178493" />
        <display value="Myopic macular degeneration" />
      </concept>
      <concept>
        <code value="ORPHA:178506" />
        <display value="Brain calcification, Rajab type" />
      </concept>
      <concept>
        <code value="ORPHA:178509" />
        <display value="Perry syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:178512" />
        <display value="Folliculotropic mycosis fungoides" />
      </concept>
      <concept>
        <code value="ORPHA:178517" />
        <display value="Localized pagetoid reticulosis" />
      </concept>
      <concept>
        <code value="ORPHA:178522" />
        <display value="Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178528" />
        <display value="Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178533" />
        <display value="Primary cutaneous gamma/delta-positive T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178536" />
        <display value="Primary cutaneous marginal zone B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178540" />
        <display value="Primary cutaneous follicle center lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178544" />
        <display value="Primary cutaneous diffuse large B-cell lymphoma, leg type" />
      </concept>
      <concept>
        <code value="ORPHA:178548" />
        <display value="Indolent primary cutaneous T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178551" />
        <display value="Aggressive primary cutaneous T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178554" />
        <display value="Aggressive primary cutaneous B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178557" />
        <display value="Indolent primary cutaneous B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178563" />
        <display value="Primary cutaneous B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:178566" />
        <display value="Mycosis fungoides and variants" />
      </concept>
      <concept>
        <code value="ORPHA:1786" />
        <display value="Acrofacial dysostosis, Catania type" />
      </concept>
      <concept>
        <code value="ORPHA:1787" />
        <display value="Acrofacial dysostosis, Palagonia type" />
      </concept>
      <concept>
        <code value="ORPHA:1788" />
        <display value="Acrofacial dysostosis, Rodriguez type" />
      </concept>
      <concept>
        <code value="ORPHA:178996" />
        <display value="Acquired neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:179" />
        <display value="Birdshot chorioretinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1790" />
        <display value="Hypomandibular faciocranial dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:179006" />
        <display value="Primary immunodeficiency due to a defect in adaptive immunity" />
      </concept>
      <concept>
        <code value="ORPHA:1791" />
        <display value="Frontofacionasal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1794" />
        <display value="Oculomaxillofacial dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:179490" />
        <display value="Obesity due to congenital leptin resistance" />
      </concept>
      <concept>
        <code value="ORPHA:179494" />
        <display value="Obesity due to leptin receptor gene deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1795" />
        <display value="Peripheral dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:1797" />
        <display value="Autosomal dominant spondylocostal dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:1798" />
        <display value="Dysostosis, Stanescu type" />
      </concept>
      <concept>
        <code value="ORPHA:1799" />
        <display value="Familial developmental dysphasia" />
      </concept>
      <concept>
        <code value="ORPHA:18" />
        <display value="Distal renal tubular acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:180" />
        <display value="Choroideremia" />
      </concept>
      <concept>
        <code value="ORPHA:180062" />
        <display value="Uterovaginal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:180065" />
        <display value="Non-syndromic uterovaginal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:180068" />
        <display value="Partial bilateral aplasia of the Mullerian ducts" />
      </concept>
      <concept>
        <code value="ORPHA:180071" />
        <display value="Unilateral aplasia of the Mullerian ducts" />
      </concept>
      <concept>
        <code value="ORPHA:180074" />
        <display value="True unicornuate uterus" />
      </concept>
      <concept>
        <code value="ORPHA:180079" />
        <display value="Pseudounicornuate uterus" />
      </concept>
      <concept>
        <code value="ORPHA:180086" />
        <display value="Didelphys uterus" />
      </concept>
      <concept>
        <code value="ORPHA:1801" />
        <display value="Kyphomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:180106" />
        <display value="Bicervical bicornuate uterus and blind hemivagina" />
      </concept>
      <concept>
        <code value="ORPHA:180111" />
        <display value="Bicervical bicornuate uterus with patent cervix and vagina" />
      </concept>
      <concept>
        <code value="ORPHA:180114" />
        <display value="Unicervical bicornuate uterus" />
      </concept>
      <concept>
        <code value="ORPHA:180118" />
        <display value="Cordiform uterus" />
      </concept>
      <concept>
        <code value="ORPHA:180122" />
        <display value="Septate uterus" />
      </concept>
      <concept>
        <code value="ORPHA:180126" />
        <display value="Complete septate uterus" />
      </concept>
      <concept>
        <code value="ORPHA:180129" />
        <display value="Partial septate uterus" />
      </concept>
      <concept>
        <code value="ORPHA:180134" />
        <display value="Bicornuate uterus" />
      </concept>
      <concept>
        <code value="ORPHA:180139" />
        <display value="Uterine hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:180142" />
        <display value="Agenesis and aplasia of uterine body" />
      </concept>
      <concept>
        <code value="ORPHA:180145" />
        <display value="Uterine cervical aplasia and agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:180148" />
        <display value="Syndromic uterovaginal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:180151" />
        <display value="Rare vaginal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:180154" />
        <display value="Septate vagina" />
      </concept>
      <concept>
        <code value="ORPHA:180157" />
        <display value="Longitudinal vaginal septum" />
      </concept>
      <concept>
        <code value="ORPHA:180160" />
        <display value="Transverse vaginal septum" />
      </concept>
      <concept>
        <code value="ORPHA:180163" />
        <display value="Rare breast malformation" />
      </concept>
      <concept>
        <code value="ORPHA:180170" />
        <display value="Excess breast volume or number" />
      </concept>
      <concept>
        <code value="ORPHA:180173" />
        <display value="Deficient breast volume or number" />
      </concept>
      <concept>
        <code value="ORPHA:180176" />
        <display value="Familial juvenile hypertrophy of the breast" />
      </concept>
      <concept>
        <code value="ORPHA:180182" />
        <display value="Supernumerary breasts" />
      </concept>
      <concept>
        <code value="ORPHA:180188" />
        <display value="Isolated congenital breast hypoplasia/aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:180193" />
        <display value="Syndromic breast hypoplasia/aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:180199" />
        <display value="Rare non-malformative gynecologic or obstetric disease" />
      </concept>
      <concept>
        <code value="ORPHA:1802" />
        <display value="Ghosal hematodiaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:180202" />
        <display value="Rare non-malformative breast disease" />
      </concept>
      <concept>
        <code value="ORPHA:180205" />
        <display value="Rare non-malformative uterovaginal or vulvovaginal disease" />
      </concept>
      <concept>
        <code value="ORPHA:180208" />
        <display value="Anomaly of puberty or/and menstrual cycle" />
      </concept>
      <concept>
        <code value="ORPHA:180220" />
        <display value="Rare uterine adnexal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:180226" />
        <display value="Embryonal carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:180229" />
        <display value="Polyembryoma" />
      </concept>
      <concept>
        <code value="ORPHA:180234" />
        <display value="Mixed germ cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:180237" />
        <display value="Benign tumor of fallopian tubes" />
      </concept>
      <concept>
        <code value="ORPHA:180242" />
        <display value="Malignant tumor of fallopian tubes" />
      </concept>
      <concept>
        <code value="ORPHA:180247" />
        <display value="Vaginal carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:180250" />
        <display value="Rare breast tumor" />
      </concept>
      <concept>
        <code value="ORPHA:180253" />
        <display value="Rare benign breast tumor" />
      </concept>
      <concept>
        <code value="ORPHA:180257" />
        <display value="Rare malignant breast tumor" />
      </concept>
      <concept>
        <code value="ORPHA:180261" />
        <display value="Phyllodes tumor of the breast" />
      </concept>
      <concept>
        <code value="ORPHA:180267" />
        <display value="Giant adenofibroma of the breast" />
      </concept>
      <concept>
        <code value="ORPHA:180275" />
        <display value="Paget disease of the nipple" />
      </concept>
      <concept>
        <code value="ORPHA:1803" />
        <display value="Thoracomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:180303" />
        <display value="Rare non-malformative uterine adnexal disease" />
      </concept>
      <concept>
        <code value="ORPHA:180312" />
        <display value="Rare vulvovaginal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:1806" />
        <display value="Ectodermal dysplasia-blindness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1807" />
        <display value="Focal facial dermal dysplasia type III" />
      </concept>
      <concept>
        <code value="ORPHA:180766" />
        <display value="Malformative syndrome with dentinogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:180772" />
        <display value="Rare disease with autism" />
      </concept>
      <concept>
        <code value="ORPHA:180776" />
        <display value="Non-syndromic diaphragmatic or thoracic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:180779" />
        <display value="Syndromic diaphragmatic or thoracic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:1808" />
        <display value="Hidrotic ectodermal dysplasia, Christianson-Fourie type" />
      </concept>
      <concept>
        <code value="ORPHA:180821" />
        <display value="Rare gastroesophageal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:180824" />
        <display value="Rare tumor of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:1809" />
        <display value="Hidrotic ectodermal dysplasia, Halal type" />
      </concept>
      <concept>
        <code value="ORPHA:181" />
        <display value="X-linked hypohidrotic ectodermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1810" />
        <display value="Autosomal dominant hypohidrotic ectodermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1811" />
        <display value="Odontomicronychial dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1812" />
        <display value="Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:181368" />
        <display value="Rare insulin-resistance syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:181371" />
        <display value="Rare diabetes mellitus type 1" />
      </concept>
      <concept>
        <code value="ORPHA:181376" />
        <display value="Rare diabetes mellitus type 2" />
      </concept>
      <concept>
        <code value="ORPHA:181381" />
        <display value="Other rare diabetes mellitus" />
      </concept>
      <concept>
        <code value="ORPHA:181384" />
        <display value="Rare hypothalamic or pituitary disease" />
      </concept>
      <concept>
        <code value="ORPHA:181387" />
        <display value="Rare disorder with hypogonadotropic hypogonadism" />
      </concept>
      <concept>
        <code value="ORPHA:181390" />
        <display value="Hypogonadotropic hypogonadism associated with other endocrinopathies" />
      </concept>
      <concept>
        <code value="ORPHA:181393" />
        <display value="Growth hormone insensitivity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:181396" />
        <display value="Rare hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:181399" />
        <display value="Rare hyperthyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:181402" />
        <display value="Syndrome with hypoparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:181405" />
        <display value="Rare hypoparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:181408" />
        <display value="Rare hyperparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:181412" />
        <display value="Adrenogenital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:181415" />
        <display value="Rare primary hyperaldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:181419" />
        <display value="Rare hypoaldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:181422" />
        <display value="Rare hyperlipidemia" />
      </concept>
      <concept>
        <code value="ORPHA:181425" />
        <display value="Major hypertriglyceridemia" />
      </concept>
      <concept>
        <code value="ORPHA:181428" />
        <display value="Hyperalphalipoproteinemia" />
      </concept>
      <concept>
        <code value="ORPHA:181431" />
        <display value="Rare hypolipidemia" />
      </concept>
      <concept>
        <code value="ORPHA:181437" />
        <display value="Rare syndromic dyslipidemia" />
      </concept>
      <concept>
        <code value="ORPHA:181441" />
        <display value="Rare disorder with hypergonadotropic hypogonadism" />
      </concept>
      <concept>
        <code value="ORPHA:1816" />
        <display value="Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1818" />
        <display value="Ectodermal dysplasia, trichoodontoonychial type" />
      </concept>
      <concept>
        <code value="ORPHA:1819" />
        <display value="Epimetaphyseal skeletal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:182" />
        <display value="Chromomycosis" />
      </concept>
      <concept>
        <code value="ORPHA:182040" />
        <display value="Aplastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:182043" />
        <display value="Rare constitutional hemolytic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:182047" />
        <display value="Rare acquired hemolytic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:182050" />
        <display value="MYH9-related disease" />
      </concept>
      <concept>
        <code value="ORPHA:182054" />
        <display value="Rare thrombotic disease of hematologic origin" />
      </concept>
      <concept>
        <code value="ORPHA:182058" />
        <display value="Primary orthostatic hypotension" />
      </concept>
      <concept>
        <code value="ORPHA:182061" />
        <display value="Cerebellar malformation" />
      </concept>
      <concept>
        <code value="ORPHA:182064" />
        <display value="Rare neuroinflammatory or neuroimmunological disease" />
      </concept>
      <concept>
        <code value="ORPHA:182067" />
        <display value="Glial tumor" />
      </concept>
      <concept>
        <code value="ORPHA:182070" />
        <display value="Rare neurodegenerative disease" />
      </concept>
      <concept>
        <code value="ORPHA:182073" />
        <display value="Syndromic neurometabolic disease with non-X-linked intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:182076" />
        <display value="Syndromic neurometabolic disease with X-linked intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:182079" />
        <display value="ARX-related epileptic encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:182083" />
        <display value="Channelopathy with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:182086" />
        <display value="Acquired peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:182090" />
        <display value="Pulmonary arterial hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:182095" />
        <display value="Interstitial lung disease" />
      </concept>
      <concept>
        <code value="ORPHA:182098" />
        <display value="Pneumoconiosis" />
      </concept>
      <concept>
        <code value="ORPHA:182101" />
        <display value="Idiopathic eosinophilic pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:182104" />
        <display value="Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease" />
      </concept>
      <concept>
        <code value="ORPHA:182108" />
        <display value="Thoracic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:182111" />
        <display value="Respiratory malformation" />
      </concept>
      <concept>
        <code value="ORPHA:182114" />
        <display value="Rare urogenital tumor" />
      </concept>
      <concept>
        <code value="ORPHA:182117" />
        <display value="Non-syndromic urogenital tract malformation of female" />
      </concept>
      <concept>
        <code value="ORPHA:182121" />
        <display value="Non-syndromic urogenital tract malformation of male" />
      </concept>
      <concept>
        <code value="ORPHA:182124" />
        <display value="Non-syndromic urogenital tract malformation of male and female" />
      </concept>
      <concept>
        <code value="ORPHA:182127" />
        <display value="Extragonadal germinoma" />
      </concept>
      <concept>
        <code value="ORPHA:182130" />
        <display value="Tumor of endocrine glands" />
      </concept>
      <concept>
        <code value="ORPHA:1822" />
        <display value="Dysplasia epiphysealis hemimelica" />
      </concept>
      <concept>
        <code value="ORPHA:182222" />
        <display value="Rare systemic disease" />
      </concept>
      <concept>
        <code value="ORPHA:182228" />
        <display value="Systemic autoimmune disease" />
      </concept>
      <concept>
        <code value="ORPHA:182231" />
        <display value="Rare rheumatologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:1824" />
        <display value="Lowry-Wood syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1825" />
        <display value="Epiphyseal dysplasia-hearing loss-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1826" />
        <display value="Frontometaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1827" />
        <display value="Acromelic frontonasal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:182734" />
        <display value="Genetic urticaria" />
      </concept>
      <concept>
        <code value="ORPHA:183" />
        <display value="Eosinophilic granulomatosis with polyangiitis" />
      </concept>
      <concept>
        <code value="ORPHA:1830" />
        <display value="Schimke immuno-osseous dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1832" />
        <display value="Lethal osteosclerotic bone dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1834" />
        <display value="Axial mesodermal dysplasia spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:183422" />
        <display value="Polymalformative genetic syndrome with increased risk of developing cancer" />
      </concept>
      <concept>
        <code value="ORPHA:183426" />
        <display value="Genetic epidermal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:183435" />
        <display value="Inherited ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:183438" />
        <display value="Genetic erythrokeratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:183441" />
        <display value="Genetic acrokeratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:183444" />
        <display value="Genetic porokeratosis" />
      </concept>
      <concept>
        <code value="ORPHA:183447" />
        <display value="Genetic epidermal appendage anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:183450" />
        <display value="Genetic hair anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:183454" />
        <display value="Genetic nail anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:183460" />
        <display value="Genetic sebaceous gland anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:183463" />
        <display value="Genetic pigmentation anomaly of the skin" />
      </concept>
      <concept>
        <code value="ORPHA:183466" />
        <display value="Genetic hyperpigmentation of the skin" />
      </concept>
      <concept>
        <code value="ORPHA:183469" />
        <display value="Genetic hypopigmentation of the skin" />
      </concept>
      <concept>
        <code value="ORPHA:183472" />
        <display value="Genetic dermis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:183478" />
        <display value="Genetic skin vascular disorder" />
      </concept>
      <concept>
        <code value="ORPHA:183481" />
        <display value="Genetic mixed dermis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:183484" />
        <display value="Genetic subcutaneous tissue disorder" />
      </concept>
      <concept>
        <code value="ORPHA:183487" />
        <display value="Genetic skin tumor" />
      </concept>
      <concept>
        <code value="ORPHA:183490" />
        <display value="Genetic photodermatosis" />
      </concept>
      <concept>
        <code value="ORPHA:183494" />
        <display value="Genetic immune deficiency with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:183497" />
        <display value="Genetic neuromuscular disease" />
      </concept>
      <concept>
        <code value="ORPHA:183500" />
        <display value="Genetic neurodegenerative disease" />
      </concept>
      <concept>
        <code value="ORPHA:183503" />
        <display value="Genetic central nervous system and retinal vascular disease" />
      </concept>
      <concept>
        <code value="ORPHA:183506" />
        <display value="Genetic central nervous system malformation" />
      </concept>
      <concept>
        <code value="ORPHA:183509" />
        <display value="Rare genetic headache" />
      </concept>
      <concept>
        <code value="ORPHA:183512" />
        <display value="Rare genetic epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:183515" />
        <display value="Rare genetic medullar disease" />
      </concept>
      <concept>
        <code value="ORPHA:183518" />
        <display value="Rare hereditary ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:183521" />
        <display value="Rare genetic movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:183524" />
        <display value="Rare genetic bone disease" />
      </concept>
      <concept>
        <code value="ORPHA:183527" />
        <display value="Genetic bone tumor" />
      </concept>
      <concept>
        <code value="ORPHA:183530" />
        <display value="Rare genetic developmental defect during embryogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:183533" />
        <display value="Genetic multiple congenital anomalies/dysmorphic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:183536" />
        <display value="Genetic congenital limb malformation" />
      </concept>
      <concept>
        <code value="ORPHA:183539" />
        <display value="Genetic renal or urinary tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:183542" />
        <display value="Genetic cranial malformation" />
      </concept>
      <concept>
        <code value="ORPHA:183545" />
        <display value="Genetic digestive tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:183548" />
        <display value="Genetic visceral malformation of the liver, biliary tract, pancreas or spleen" />
      </concept>
      <concept>
        <code value="ORPHA:183554" />
        <display value="Genetic respiratory or mediastinal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:183557" />
        <display value="Genetic developmental defect of the eye" />
      </concept>
      <concept>
        <code value="ORPHA:183570" />
        <display value="Genetic malformation syndrome with short stature" />
      </concept>
      <concept>
        <code value="ORPHA:183573" />
        <display value="Genetic overgrowth/obesity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:183576" />
        <display value="Genetic branchial arch or oral-acral syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:183580" />
        <display value="Genetic malformation syndrome with odontal and/or periodontal component" />
      </concept>
      <concept>
        <code value="ORPHA:183583" />
        <display value="Genetic head and neck malformation" />
      </concept>
      <concept>
        <code value="ORPHA:183586" />
        <display value="Genetic glomerular disease" />
      </concept>
      <concept>
        <code value="ORPHA:183589" />
        <display value="Genetic thrombotic microangiopathy" />
      </concept>
      <concept>
        <code value="ORPHA:183592" />
        <display value="Genetic renal tubular disease" />
      </concept>
      <concept>
        <code value="ORPHA:183595" />
        <display value="Genetic renal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:1836" />
        <display value="Mesomelic dysplasia, Kantaputra type" />
      </concept>
      <concept>
        <code value="ORPHA:183607" />
        <display value="Genetic lens and zonula anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:183616" />
        <display value="Genetic neuro-ophthalmological disease" />
      </concept>
      <concept>
        <code value="ORPHA:183619" />
        <display value="Genetic eye tumor" />
      </concept>
      <concept>
        <code value="ORPHA:183622" />
        <display value="Genetic respiratory malformation" />
      </concept>
      <concept>
        <code value="ORPHA:183625" />
        <display value="Rare genetic diabetes mellitus" />
      </concept>
      <concept>
        <code value="ORPHA:183628" />
        <display value="Rare genetic hypothalamic or pituitary disease" />
      </concept>
      <concept>
        <code value="ORPHA:183631" />
        <display value="Rare genetic thyroid disease" />
      </concept>
      <concept>
        <code value="ORPHA:183634" />
        <display value="Rare genetic parathyroid disease and phosphocalcic metabolism disorder" />
      </concept>
      <concept>
        <code value="ORPHA:183637" />
        <display value="Rare genetic adrenal disease" />
      </concept>
      <concept>
        <code value="ORPHA:183643" />
        <display value="Genetic polyendocrinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:183651" />
        <display value="Rare constitutional anemia" />
      </concept>
      <concept>
        <code value="ORPHA:183654" />
        <display value="Rare genetic coagulation disorder" />
      </concept>
      <concept>
        <code value="ORPHA:183660" />
        <display value="Severe combined immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:183663" />
        <display value="Hyper-IgM syndrome with susceptibility to opportunistic infections" />
      </concept>
      <concept>
        <code value="ORPHA:183666" />
        <display value="Hyper-IgM syndrome without susceptibility to opportunistic infections" />
      </concept>
      <concept>
        <code value="ORPHA:183669" />
        <display value="Agammaglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:183675" />
        <display value="Recurrent infections associated with rare immunoglobulin isotypes deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:183678" />
        <display value="Hermansky-Pudlak syndrome with neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:183681" />
        <display value="Functional neutrophil defect" />
      </concept>
      <concept>
        <code value="ORPHA:1837" />
        <display value="Ulna metaphyseal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:183707" />
        <display value="Neutrophil immunodeficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:183710" />
        <display value="Genetic susceptibility to infections due to particular pathogens" />
      </concept>
      <concept>
        <code value="ORPHA:183713" />
        <display value="Pyogenic bacterial infections due to MyD88 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:183731" />
        <display value="Rare genetic gynecological and obstetrical diseases" />
      </concept>
      <concept>
        <code value="ORPHA:183734" />
        <display value="Genetic gynecological tumor" />
      </concept>
      <concept>
        <code value="ORPHA:183757" />
        <display value="Rare genetic intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:183763" />
        <display value="Rare genetic syndromic intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:183770" />
        <display value="Rare genetic immune disease" />
      </concept>
      <concept>
        <code value="ORPHA:1839" />
        <display value="Hereditary mucoepithelial dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:184" />
        <display value="Cherubism" />
      </concept>
      <concept>
        <code value="ORPHA:1842" />
        <display value="Bone dysplasia, lethal Holmgren type" />
      </concept>
      <concept>
        <code value="ORPHA:1848" />
        <display value="Renal agenesis, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:1849" />
        <display value="Infundibulopelvic stenosis-multicystic kidney syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:185" />
        <display value="Scimitar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1851" />
        <display value="Multicystic dysplastic kidney" />
      </concept>
      <concept>
        <code value="ORPHA:1852" />
        <display value="X-linked retinal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1855" />
        <display value="Spondyloenchondrodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1856" />
        <display value="Spondyloperipheral dysplasia-short ulna syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1858" />
        <display value="Skeletal dysplasia-epilepsy-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:186" />
        <display value="Primary biliary cholangitis" />
      </concept>
      <concept>
        <code value="ORPHA:1860" />
        <display value="Thanatophoric dysplasia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:1861" />
        <display value="Thoracic dysplasia-hydrocephalus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1864" />
        <display value="Congenital valvular dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1865" />
        <display value="Dyssegmental dysplasia, Silverman-Handmaker type" />
      </concept>
      <concept>
        <code value="ORPHA:1866" />
        <display value="Focal, segmental or multifocal dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:1867" />
        <display value="Bullous dystrophy, macular type" />
      </concept>
      <concept>
        <code value="ORPHA:187" />
        <display value="Citrullinemia" />
      </concept>
      <concept>
        <code value="ORPHA:1871" />
        <display value="Progressive cone dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1872" />
        <display value="Cone rod dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1873" />
        <display value="Jalili syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1875" />
        <display value="Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1876" />
        <display value="Oculogastrointestinal muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:1877" />
        <display value="Muscular dystrophy-white matter spongiosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1878" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2H" />
      </concept>
      <concept>
        <code value="ORPHA:1879" />
        <display value="Melorheostosis with osteopoikilosis" />
      </concept>
      <concept>
        <code value="ORPHA:188" />
        <display value="Systemic capillary leak syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1880" />
        <display value="Ebstein malformation" />
      </concept>
      <concept>
        <code value="ORPHA:1882" />
        <display value="Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1883" />
        <display value="Ectodermal dysplasia-sensorineural deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1884" />
        <display value="Ectopia lentis-chorioretinal dystrophy-myopia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1885" />
        <display value="Isolated ectopia lentis" />
      </concept>
      <concept>
        <code value="ORPHA:189" />
        <display value="Hidrotic ectodermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1891" />
        <display value="Intellectual disability-spasticity-ectrodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1892" />
        <display value="Ectrodactyly-polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:189427" />
        <display value="Cushing syndrome due to macronodular adrenal hyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:189439" />
        <display value="Primary pigmented nodular adrenocortical disease" />
      </concept>
      <concept>
        <code value="ORPHA:189466" />
        <display value="Familial isolated hypoparathyroidism due to impaired PTH secretion" />
      </concept>
      <concept>
        <code value="ORPHA:1895" />
        <display value="Edinburgh malformation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1896" />
        <display value="EEC syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1897" />
        <display value="EEM syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1899" />
        <display value="Ehlers-Danlos syndrome, arthrochalasis type" />
      </concept>
      <concept>
        <code value="ORPHA:19" />
        <display value="2-hydroxyglutaric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:190" />
        <display value="Coats disease" />
      </concept>
      <concept>
        <code value="ORPHA:1900" />
        <display value="Ehlers-Danlos syndrome, kyphoscoliotic type" />
      </concept>
      <concept>
        <code value="ORPHA:1901" />
        <display value="Ehlers-Danlos syndrome, dermatosparaxis type" />
      </concept>
      <concept>
        <code value="ORPHA:1902" />
        <display value="Ehrlichiosis" />
      </concept>
      <concept>
        <code value="ORPHA:1906" />
        <display value="Fetal valproate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1908" />
        <display value="Aminopterin/methotrexate embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1909" />
        <display value="Indomethacin embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:191" />
        <display value="Cockayne syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1910" />
        <display value="Fetal iodine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1911" />
        <display value="Cocaine embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1912" />
        <display value="Fetal hydantoin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1913" />
        <display value="Fetal trimethadione syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1914" />
        <display value="Vitamin K antagonist embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1915" />
        <display value="Fetal alcohol syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1916" />
        <display value="Diethylstilbestrol syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1917" />
        <display value="Fetal methylmercury syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1918" />
        <display value="Fetal minoxidil syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1919" />
        <display value="Phenobarbital embryopathy" />
      </concept>
      <concept>
        <code value="ORPHA:192" />
        <display value="Coffin-Lowry syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1920" />
        <display value="Toluene embryopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1923" />
        <display value="Methimazole embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1926" />
        <display value="Diabetic embryopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1927" />
        <display value="Emery-Nelson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1928" />
        <display value="Congenital lobar emphysema" />
      </concept>
      <concept>
        <code value="ORPHA:1929" />
        <display value="Rasmussen subacute encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:193" />
        <display value="Cohen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1930" />
        <display value="Herpes simplex virus encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:1931" />
        <display value="Frontal encephalocele" />
      </concept>
      <concept>
        <code value="ORPHA:1933" />
        <display value="Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:1934" />
        <display value="Early infantile epileptic encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1935" />
        <display value="Early myoclonic encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:1937" />
        <display value="Eng-Strom syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1941" />
        <display value="Juvenile absence epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:1942" />
        <display value="Myoclonic-astastic epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:1943" />
        <display value="Early-onset progressive encephalopathy with migrant continuous myoclonus" />
      </concept>
      <concept>
        <code value="ORPHA:1945" />
        <display value="Rolandic epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:1946" />
        <display value="Amelocerebrohypohidrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1947" />
        <display value="Progressive epilepsy-intellectual disability syndrome, Finnish type" />
      </concept>
      <concept>
        <code value="ORPHA:1948" />
        <display value="Epilepsy-microcephaly-skeletal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1949" />
        <display value="Benign familial neonatal epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:195" />
        <display value="Cat-eye syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1951" />
        <display value="Epilepsy-telangiectasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1952" />
        <display value="Pacman dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1954" />
        <display value="Congenital lethal erythroderma" />
      </concept>
      <concept>
        <code value="ORPHA:1955" />
        <display value="Spinocerebellar ataxia type 34" />
      </concept>
      <concept>
        <code value="ORPHA:1956" />
        <display value="Erythromelalgia" />
      </concept>
      <concept>
        <code value="ORPHA:1957" />
        <display value="Esthesioneuroblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:1959" />
        <display value="Evans syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1962" />
        <display value="Exostoses-anetodermia-brachydactyly type E syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1964" />
        <display value="Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1968" />
        <display value="Flat face-microstomia-ear anomaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1969" />
        <display value="Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1970" />
        <display value="Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1972" />
        <display value="Lethal faciocardiomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1973" />
        <display value="Faciocardiorenal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1974" />
        <display value="Autosomal recessive faciodigitogenital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1979" />
        <display value="Lipodystrophy due to peptidic growth factors deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:198" />
        <display value="Occipital horn syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1980" />
        <display value="Bilateral striopallidodentate calcinosis" />
      </concept>
      <concept>
        <code value="ORPHA:1986" />
        <display value="Gollop-Wolfgang complex" />
      </concept>
      <concept>
        <code value="ORPHA:1987" />
        <display value="Femoral agenesis/hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:1988" />
        <display value="Femoral-facial syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199" />
        <display value="Cornelia de Lange syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:1991" />
        <display value="Cleft lip with or without cleft palate" />
      </concept>
      <concept>
        <code value="ORPHA:199241" />
        <display value="Pulmonary capillary hemangiomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:199244" />
        <display value="Nelson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199247" />
        <display value="Corticosteroid-binding globulin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:199251" />
        <display value="Ledderhose disease" />
      </concept>
      <concept>
        <code value="ORPHA:199257" />
        <display value="Superficial fibromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:199260" />
        <display value="Calcifying aponeurotic fibroma" />
      </concept>
      <concept>
        <code value="ORPHA:199267" />
        <display value="Infantile digital fibromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:199276" />
        <display value="Familial multiple lipomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:199279" />
        <display value="Familial angiolipomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:199282" />
        <display value="Harlequin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199285" />
        <display value="Hereditary hypercarotenemia and vitamin A deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:199293" />
        <display value="Congenital microgastria" />
      </concept>
      <concept>
        <code value="ORPHA:199296" />
        <display value="Congenital isolated ACTH deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:199299" />
        <display value="Late-onset isolated ACTH deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:1993" />
        <display value="Pai syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199302" />
        <display value="Isolated cleft lip" />
      </concept>
      <concept>
        <code value="ORPHA:199306" />
        <display value="Cleft lip/palate" />
      </concept>
      <concept>
        <code value="ORPHA:199310" />
        <display value="Tetragametic chimerism" />
      </concept>
      <concept>
        <code value="ORPHA:199315" />
        <display value="Familial clubfoot with or without associated lower limb anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:199318" />
        <display value="15q13.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199323" />
        <display value="Endophthalmitis" />
      </concept>
      <concept>
        <code value="ORPHA:199326" />
        <display value="Isolated autosomal dominant hypomagnesemia, Glaudemans type" />
      </concept>
      <concept>
        <code value="ORPHA:199329" />
        <display value="Congenital myopathy, Paradas type" />
      </concept>
      <concept>
        <code value="ORPHA:199332" />
        <display value="Endocrine-cerebro-osteodysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199337" />
        <display value="Pancreatic insufficiency-anemia-hyperostosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199340" />
        <display value="Muscular dystrophy, Selcen type" />
      </concept>
      <concept>
        <code value="ORPHA:199343" />
        <display value="EAST syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199348" />
        <display value="Thiamine-responsive encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:199351" />
        <display value="Adult-onset dystonia-parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:199354" />
        <display value="CARASIL" />
      </concept>
      <concept>
        <code value="ORPHA:1995" />
        <display value="Cleft lip-retinopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:199627" />
        <display value="Atypical autism" />
      </concept>
      <concept>
        <code value="ORPHA:199630" />
        <display value="Isolated cerebellar vermis hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:199633" />
        <display value="Cerebral malformation" />
      </concept>
      <concept>
        <code value="ORPHA:199639" />
        <display value="Syndrome with corpus callosum agenesis/dysgenesis as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:199642" />
        <display value="Isolated congenital microcephaly" />
      </concept>
      <concept>
        <code value="ORPHA:199647" />
        <display value="Isolated encephalocele" />
      </concept>
      <concept>
        <code value="ORPHA:1997" />
        <display value="Blepharo-cheilo-odontic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:20" />
        <display value="3-hydroxy-3-methylglutaric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:200037" />
        <display value="Paroxysmal dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:2001" />
        <display value="Cleft lip/palate-intestinal malrotation-cardiopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2003" />
        <display value="Cleft lip/palate-deafness-sacral lipoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2004" />
        <display value="Laryngotracheoesophageal cleft" />
      </concept>
      <concept>
        <code value="ORPHA:200418" />
        <display value="Immunodeficiency with factor I anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:200421" />
        <display value="Immunodeficiency with factor H anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:2006" />
        <display value="Median cleft lip/mandibule" />
      </concept>
      <concept>
        <code value="ORPHA:2007" />
        <display value="Alar cartilages hypoplasia-coloboma-telecanthus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2008" />
        <display value="Acrocardiofacial syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:201" />
        <display value="Cowden syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2010" />
        <display value="Cleft palate-stapes fixation-oligodontia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2013" />
        <display value="Cleft palate-large ears-small head syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2014" />
        <display value="Cleft palate" />
      </concept>
      <concept>
        <code value="ORPHA:2015" />
        <display value="Cleft palate-short stature-vertebral anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2016" />
        <display value="Cleft palate-lateral synechia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2017" />
        <display value="Sternal cleft" />
      </concept>
      <concept>
        <code value="ORPHA:2019" />
        <display value="Femur-fibula-ulna complex" />
      </concept>
      <concept>
        <code value="ORPHA:202" />
        <display value="Crandall syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2020" />
        <display value="Congenital fiber-type disproportion myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2021" />
        <display value="Fibrochondrogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:2022" />
        <display value="Endomyocardial fibroelastosis" />
      </concept>
      <concept>
        <code value="ORPHA:2023" />
        <display value="Undifferentiated pleomorphic sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:2024" />
        <display value="Hereditary gingival fibromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:2025" />
        <display value="Gingival fibromatosis-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2026" />
        <display value="Gingival fibromatosis-hypertrichosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2027" />
        <display value="Gingival fibromatosis-progressive deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2028" />
        <display value="Juvenile hyaline fibromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:202940" />
        <display value="Anomaly of puberty or/and menstrual cycle of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:202948" />
        <display value="Syndromic microphthalmia-anophthalmia-coloboma" />
      </concept>
      <concept>
        <code value="ORPHA:2030" />
        <display value="Fibrosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:2031" />
        <display value="Hepatic fibrosis-renal cysts-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2032" />
        <display value="Idiopathic pulmonary fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:2034" />
        <display value="Filariasis" />
      </concept>
      <concept>
        <code value="ORPHA:2035" />
        <display value="Lymphatic filariasis" />
      </concept>
      <concept>
        <code value="ORPHA:2036" />
        <display value="Scalp-ear-nipple syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2037" />
        <display value="Congenital aortopulmonary window" />
      </concept>
      <concept>
        <code value="ORPHA:2038" />
        <display value="Pulmonary arteriovenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:2039" />
        <display value="Congenital systemic arteriovenous fistula" />
      </concept>
      <concept>
        <code value="ORPHA:204" />
        <display value="Sporadic Creutzfeldt-Jakob disease" />
      </concept>
      <concept>
        <code value="ORPHA:2040" />
        <display value="Congenital bronchobiliary fistula" />
      </concept>
      <concept>
        <code value="ORPHA:2041" />
        <display value="Coronary arterial fistulas" />
      </concept>
      <concept>
        <code value="ORPHA:2044" />
        <display value="Floating-Harbor syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2045" />
        <display value="FLOTCH syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2047" />
        <display value="Flynn-Aird syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:205" />
        <display value="Crigler-Najjar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2050" />
        <display value="Cole-Carpenter syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2052" />
        <display value="Fraser syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2053" />
        <display value="Freeman-Sheldon syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2054" />
        <display value="Osteochondritis of tarsal/metatarsal bone" />
      </concept>
      <concept>
        <code value="ORPHA:2056" />
        <display value="Essential fructosuria" />
      </concept>
      <concept>
        <code value="ORPHA:2057" />
        <display value="Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2059" />
        <display value="Fryns syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2062" />
        <display value="Progressive non-infectious anterior vertebral fusion" />
      </concept>
      <concept>
        <code value="ORPHA:2063" />
        <display value="Splenogonadal fusion-limb defects-micrognathia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2064" />
        <display value="Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:206428" />
        <display value="Hypoxanthine-guanine phosphoribosyltransferase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:206436" />
        <display value="Infantile Krabbe disease" />
      </concept>
      <concept>
        <code value="ORPHA:206443" />
        <display value="Late-infantile/juvenile Krabbe disease" />
      </concept>
      <concept>
        <code value="ORPHA:206448" />
        <display value="Adult Krabbe disease" />
      </concept>
      <concept>
        <code value="ORPHA:206470" />
        <display value="Serous or mucinous cystadenoma of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:206473" />
        <display value="Borderline epithelial tumor of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:206484" />
        <display value="Gonadoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:206489" />
        <display value="Malignant germ cell tumor of the vagina" />
      </concept>
      <concept>
        <code value="ORPHA:206492" />
        <display value="Vulvovaginal rhabdomyosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:2065" />
        <display value="Galloway-Mowat syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:206538" />
        <display value="Malignant non-dysgerminomatous germ cell tumor of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:206546" />
        <display value="Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers" />
      </concept>
      <concept>
        <code value="ORPHA:206549" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2L" />
      </concept>
      <concept>
        <code value="ORPHA:206554" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2M" />
      </concept>
      <concept>
        <code value="ORPHA:206559" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2N" />
      </concept>
      <concept>
        <code value="ORPHA:206564" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2O" />
      </concept>
      <concept>
        <code value="ORPHA:206569" />
        <display value="Immune-mediated necrotizing myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:206572" />
        <display value="Overlap myositis" />
      </concept>
      <concept>
        <code value="ORPHA:206575" />
        <display value="Rippling muscle disease with myasthenia gravis" />
      </concept>
      <concept>
        <code value="ORPHA:206580" />
        <display value="Autosomal recessive lower motor neuron disease with childhood onset" />
      </concept>
      <concept>
        <code value="ORPHA:206583" />
        <display value="Adult polyglucosan body disease" />
      </concept>
      <concept>
        <code value="ORPHA:206586" />
        <display value="Neurolymphomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:206594" />
        <display value="Subacute inflammatory demyelinating polyneuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:206599" />
        <display value="Isolated asymptomatic elevation of creatine phosphokinase" />
      </concept>
      <concept>
        <code value="ORPHA:2066" />
        <display value="Gamma-aminobutyric acid transaminase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:206613" />
        <display value="Infectious disease with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:206634" />
        <display value="Genetic skeletal muscle disease" />
      </concept>
      <concept>
        <code value="ORPHA:206638" />
        <display value="Acquired skeletal muscle disease" />
      </concept>
      <concept>
        <code value="ORPHA:206644" />
        <display value="Progressive muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:206647" />
        <display value="Myotonic dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:206650" />
        <display value="Autosomal dominant distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:206653" />
        <display value="Autosomal recessive distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:206656" />
        <display value="Non-dystrophic myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:206662" />
        <display value="Inclusion myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2067" />
        <display value="GAPO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:206701" />
        <display value="Bulbospinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:206704" />
        <display value="Bulbospinal muscular atrophy of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:206707" />
        <display value="Bulbospinal muscular atrophy of adult" />
      </concept>
      <concept>
        <code value="ORPHA:206710" />
        <display value="Generalized bulbospinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2069" />
        <display value="Gastrocutaneous syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:206953" />
        <display value="Muscular lipidosis" />
      </concept>
      <concept>
        <code value="ORPHA:206959" />
        <display value="Muscular glycogenosis" />
      </concept>
      <concept>
        <code value="ORPHA:206966" />
        <display value="Mitochondrial myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:206970" />
        <display value="Myotonic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:206973" />
        <display value="Congenital myotonia" />
      </concept>
      <concept>
        <code value="ORPHA:206976" />
        <display value="Periodic paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:206982" />
        <display value="Muscular tumor" />
      </concept>
      <concept>
        <code value="ORPHA:206988" />
        <display value="Infectious, fungal or parasitic myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:206991" />
        <display value="Viral myositis" />
      </concept>
      <concept>
        <code value="ORPHA:206994" />
        <display value="Bacterial myositis" />
      </concept>
      <concept>
        <code value="ORPHA:206997" />
        <display value="Parasitic myositis" />
      </concept>
      <concept>
        <code value="ORPHA:207" />
        <display value="Crouzon disease" />
      </concept>
      <concept>
        <code value="ORPHA:2070" />
        <display value="Eosinophilic gastroenteritis" />
      </concept>
      <concept>
        <code value="ORPHA:207000" />
        <display value="Fungal myositis" />
      </concept>
      <concept>
        <code value="ORPHA:207012" />
        <display value="Spinal muscular atrophy associated with central nervous system anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:207015" />
        <display value="Rare hereditary disease with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:207018" />
        <display value="Rare hereditary metabolic disease with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:207021" />
        <display value="Rare hereditary systemic disease with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:207025" />
        <display value="Rare hereditary neurologic disease with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:207028" />
        <display value="Cerebellar ataxia with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:207038" />
        <display value="Acute and subacute inflammatory demyelinating polyneuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:207046" />
        <display value="Malignant lymphoma with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:207049" />
        <display value="Qualitative or quantitative protein defects in neuromuscular diseases" />
      </concept>
      <concept>
        <code value="ORPHA:207052" />
        <display value="Qualitative or quantitative defects of sarcoglycan" />
      </concept>
      <concept>
        <code value="ORPHA:207060" />
        <display value="Qualitative or quantitative defects of alpha-sarcoglycan" />
      </concept>
      <concept>
        <code value="ORPHA:207063" />
        <display value="Qualitative or quantitative defects of beta-sarcoglycan" />
      </concept>
      <concept>
        <code value="ORPHA:207067" />
        <display value="Qualitative or quantitative defects of gamma-sarcoglycan" />
      </concept>
      <concept>
        <code value="ORPHA:207070" />
        <display value="Qualitative or quantitative defects of delta-sarcoglycan" />
      </concept>
      <concept>
        <code value="ORPHA:207073" />
        <display value="Qualitative or quantitative defects of dysferlin" />
      </concept>
      <concept>
        <code value="ORPHA:207078" />
        <display value="Qualitative or quantitative defects of caveolin-3" />
      </concept>
      <concept>
        <code value="ORPHA:207085" />
        <display value="Qualitative or quantitative defects of dystrophin" />
      </concept>
      <concept>
        <code value="ORPHA:207090" />
        <display value="Qualitative or quantitative defects of collagen 6" />
      </concept>
      <concept>
        <code value="ORPHA:207094" />
        <display value="Qualitative or quantitative defects of merosin" />
      </concept>
      <concept>
        <code value="ORPHA:207098" />
        <display value="Qualitative or quantitative defects of integrin alpha-7" />
      </concept>
      <concept>
        <code value="ORPHA:207101" />
        <display value="Qualitative or quantitative defects of perlecan" />
      </concept>
      <concept>
        <code value="ORPHA:207104" />
        <display value="Qualitative or quantitative defects of calpain" />
      </concept>
      <concept>
        <code value="ORPHA:207107" />
        <display value="Qualitative or quantitative defects of TRIM32" />
      </concept>
      <concept>
        <code value="ORPHA:207110" />
        <display value="Qualitative or quantitative defects of myotubularin" />
      </concept>
      <concept>
        <code value="ORPHA:207113" />
        <display value="Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan" />
      </concept>
      <concept>
        <code value="ORPHA:207119" />
        <display value="Qualitative or quantitative defects of FKRP" />
      </concept>
      <concept>
        <code value="ORPHA:207122" />
        <display value="Qualitative or quantitative defects of fukutin" />
      </concept>
      <concept>
        <code value="ORPHA:2072" />
        <display value="Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2073" />
        <display value="Narcolepsy type 1" />
      </concept>
      <concept>
        <code value="ORPHA:2074" />
        <display value="Gemignani syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2075" />
        <display value="Genitopalatocardiac syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2076" />
        <display value="X-linked intellectual disability-epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2077" />
        <display value="German syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2078" />
        <display value="Geroderma osteodysplastica" />
      </concept>
      <concept>
        <code value="ORPHA:2081" />
        <display value="Cerebral gigantism-jaw cysts syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2083" />
        <display value="Prominent glabella-microcephaly-hypogenitalism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2084" />
        <display value="Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:208441" />
        <display value="Bilateral parasagittal parieto-occipital polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:208444" />
        <display value="Bilateral frontal polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:208447" />
        <display value="Bilateral generalized polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:2085" />
        <display value="Glaucoma-sleep apnea syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:208508" />
        <display value="Autosomal dominant cerebellar ataxia type II" />
      </concept>
      <concept>
        <code value="ORPHA:208513" />
        <display value="Spinocerebellar ataxia type 29" />
      </concept>
      <concept>
        <code value="ORPHA:208524" />
        <display value="Herpetiform pemphigus" />
      </concept>
      <concept>
        <code value="ORPHA:208593" />
        <display value="Genetic hypoparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:208596" />
        <display value="Genetic hyperparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:2086" />
        <display value="Optic pathway glioma" />
      </concept>
      <concept>
        <code value="ORPHA:208650" />
        <display value="Cryopyrin-associated periodic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2088" />
        <display value="Glycogen storage disease due to GLUT2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2089" />
        <display value="Glycogen storage disease due to hepatic glycogen synthase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:208974" />
        <display value="Chronic acquired demyelinating polyneuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:208978" />
        <display value="Chronic polyradiculoneuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:208981" />
        <display value="Polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:208984" />
        <display value="Acquired sensory ganglionopathy" />
      </concept>
      <concept>
        <code value="ORPHA:208989" />
        <display value="Non-paraneoplastic sensory ganglionopathy" />
      </concept>
      <concept>
        <code value="ORPHA:208999" />
        <display value="Paraneoplastic sensory ganglionopathy" />
      </concept>
      <concept>
        <code value="ORPHA:209" />
        <display value="Cutis laxa" />
      </concept>
      <concept>
        <code value="ORPHA:2090" />
        <display value="GMS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:209004" />
        <display value="Axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy" />
      </concept>
      <concept>
        <code value="ORPHA:209007" />
        <display value="Systemic inflammatory disease associated with an acquired peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:209010" />
        <display value="Peripheral neuropathy associated with monoclonal gammopathy" />
      </concept>
      <concept>
        <code value="ORPHA:209013" />
        <display value="Acquired amyloid peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:209016" />
        <display value="Hematological disease associated with an acquired peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:209019" />
        <display value="Solid tumor associated with an acquired peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:209024" />
        <display value="Qualitative or quantitative defects of protein O-mannose beta1,2N-acetylglucosaminyltransferase" />
      </concept>
      <concept>
        <code value="ORPHA:209027" />
        <display value="Qualitative or quantitative defects of protein glycosyltransferase-like" />
      </concept>
      <concept>
        <code value="ORPHA:209030" />
        <display value="Qualitative or quantitative defects of protein O-mannosyltransferase 1" />
      </concept>
      <concept>
        <code value="ORPHA:209033" />
        <display value="Qualitative or quantitative defects of protein O-mannosyltransferase 2" />
      </concept>
      <concept>
        <code value="ORPHA:209038" />
        <display value="Qualitative or quantitative defects of myofibrillar proteins" />
      </concept>
      <concept>
        <code value="ORPHA:209041" />
        <display value="Qualitative or quantitative defects of desmin" />
      </concept>
      <concept>
        <code value="ORPHA:209044" />
        <display value="Qualitative or quantitative defects of alphaB-cristallin" />
      </concept>
      <concept>
        <code value="ORPHA:209047" />
        <display value="Qualitative or quantitative defects of filamin C" />
      </concept>
      <concept>
        <code value="ORPHA:209050" />
        <display value="Qualitative or quantitative defects of protein ZASP" />
      </concept>
      <concept>
        <code value="ORPHA:209053" />
        <display value="Qualitative or quantitative defects of titin" />
      </concept>
      <concept>
        <code value="ORPHA:209056" />
        <display value="Qualitative or quantitative defects of telethonin" />
      </concept>
      <concept>
        <code value="ORPHA:209059" />
        <display value="Qualitative or quantitative defects of alpha-actin" />
      </concept>
      <concept>
        <code value="ORPHA:2091" />
        <display value="Multinodular goiter-cystic kidney-polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:209182" />
        <display value="Qualitative or quantitative defects of nebulin" />
      </concept>
      <concept>
        <code value="ORPHA:209185" />
        <display value="Qualitative or quantitative defects of beta-myosin heavy chain (MYH7)" />
      </concept>
      <concept>
        <code value="ORPHA:209188" />
        <display value="Qualitative or quantitative defects of emerin" />
      </concept>
      <concept>
        <code value="ORPHA:209193" />
        <display value="Qualitative or quantitative defects of selenoprotein N1" />
      </concept>
      <concept>
        <code value="ORPHA:209196" />
        <display value="Qualitative or quantitative defects of plectin" />
      </concept>
      <concept>
        <code value="ORPHA:209199" />
        <display value="Qualitative or quantitative defects of protein SERCA1" />
      </concept>
      <concept>
        <code value="ORPHA:2092" />
        <display value="Focal dermal hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:209203" />
        <display value="Qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase -" />
      </concept>
      <concept>
        <code value="ORPHA:209224" />
        <display value="Qualitative or quantitative defects of myotilin" />
      </concept>
      <concept>
        <code value="ORPHA:209335" />
        <display value="Autosomal dominant adult-onset proximal spinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:209341" />
        <display value="Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures" />
      </concept>
      <concept>
        <code value="ORPHA:209370" />
        <display value="Severe neonatal-onset encephalopathy with microcephaly" />
      </concept>
      <concept>
        <code value="ORPHA:2095" />
        <display value="Gorlin-Chaudhry-Moss syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2097" />
        <display value="Grant syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2098" />
        <display value="Acromesomelic dysplasia, Grebe type" />
      </concept>
      <concept>
        <code value="ORPHA:209867" />
        <display value="Autosomal dominant rhegmatogenous retinal detachment" />
      </concept>
      <concept>
        <code value="ORPHA:209886" />
        <display value="Familial juvenile hyperuricemic nephropathy type 1" />
      </concept>
      <concept>
        <code value="ORPHA:209902" />
        <display value="Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:209905" />
        <display value="Brain-lung-thyroid syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:209908" />
        <display value="Childhood apraxia of speech" />
      </concept>
      <concept>
        <code value="ORPHA:209916" />
        <display value="Extraskeletal myxoid chondrosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:209919" />
        <display value="Idiopathic copper-associated cirrhosis" />
      </concept>
      <concept>
        <code value="ORPHA:209932" />
        <display value="Cone dystrophy with supernormal rod response" />
      </concept>
      <concept>
        <code value="ORPHA:209943" />
        <display value="IRVAN syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:209951" />
        <display value="Autosomal recessive spastic paraplegia type 18" />
      </concept>
      <concept>
        <code value="ORPHA:209956" />
        <display value="Idiopathic uveal effusion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:209959" />
        <display value="Phacoanaphylactic uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:209964" />
        <display value="Solitary rectal ulcer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:209967" />
        <display value="Episodic ataxia type 6" />
      </concept>
      <concept>
        <code value="ORPHA:209970" />
        <display value="Episodic ataxia type 7" />
      </concept>
      <concept>
        <code value="ORPHA:209973" />
        <display value="Benign nocturnal alternating hemiplegia of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:209978" />
        <display value="Alternating hemiplegia" />
      </concept>
      <concept>
        <code value="ORPHA:209981" />
        <display value="IRIDA syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:209989" />
        <display value="Non-papillary transitional cell carcinoma of the bladder" />
      </concept>
      <concept>
        <code value="ORPHA:210" />
        <display value="Cyclosporosis" />
      </concept>
      <concept>
        <code value="ORPHA:2101" />
        <display value="Grubben-de Cock-Borghgraef syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:210110" />
        <display value="Intermediate osteopetrosis" />
      </concept>
      <concept>
        <code value="ORPHA:210115" />
        <display value="Sterile multifocal osteomyelitis with periostitis and pustulosis" />
      </concept>
      <concept>
        <code value="ORPHA:210122" />
        <display value="Congenital alveolar capillary dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:210128" />
        <display value="Urocanic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:210133" />
        <display value="Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:210136" />
        <display value="Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:210141" />
        <display value="Inherited congenital spastic tetraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:210144" />
        <display value="Lethal polymalformative syndrome, Boissel type" />
      </concept>
      <concept>
        <code value="ORPHA:210159" />
        <display value="Adult hepatocellular carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:210163" />
        <display value="Congenital lethal myopathy, Compton-North type" />
      </concept>
      <concept>
        <code value="ORPHA:2102" />
        <display value="GTP cyclohydrolase I deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:210272" />
        <display value="Mal de debarquement" />
      </concept>
      <concept>
        <code value="ORPHA:2103" />
        <display value="Guillain-Barre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2104" />
        <display value="Dysmorphism-pectus carinatum-joint laxity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:210548" />
        <display value="Macrocephaly-intellectual disability-autism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:210571" />
        <display value="Dystonia 16" />
      </concept>
      <concept>
        <code value="ORPHA:210576" />
        <display value="Congenital temporomandibular joint ankylosis" />
      </concept>
      <concept>
        <code value="ORPHA:210581" />
        <display value="Temporomandibular joint anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:210584" />
        <display value="Spindle cell hemangioma" />
      </concept>
      <concept>
        <code value="ORPHA:210589" />
        <display value="Infantile hemangioma of rare localization" />
      </concept>
      <concept>
        <code value="ORPHA:2107" />
        <display value="Hall-Riggs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2108" />
        <display value="Hallermann-Streiff syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:211" />
        <display value="Familial cylindromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:2110" />
        <display value="Hallux varus-preaxial polysyndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:211017" />
        <display value="Spinocerebellar ataxia type 30" />
      </concept>
      <concept>
        <code value="ORPHA:211037" />
        <display value="Autosomal dominant proximal spinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:211047" />
        <display value="Specific learning disability" />
      </concept>
      <concept>
        <code value="ORPHA:211053" />
        <display value="Specific language disorder" />
      </concept>
      <concept>
        <code value="ORPHA:211062" />
        <display value="Hereditary episodic ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:211067" />
        <display value="Episodic ataxia type 5" />
      </concept>
      <concept>
        <code value="ORPHA:2111" />
        <display value="Cystic hamartoma of lung and kidney" />
      </concept>
      <concept>
        <code value="ORPHA:211237" />
        <display value="Rare vascular tumor" />
      </concept>
      <concept>
        <code value="ORPHA:211240" />
        <display value="Genetic vascular anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:211243" />
        <display value="Simple vascular malformation" />
      </concept>
      <concept>
        <code value="ORPHA:211247" />
        <display value="Rare capillary malformation" />
      </concept>
      <concept>
        <code value="ORPHA:211252" />
        <display value="Rare venous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:211255" />
        <display value="Rare lymphatic system malformation" />
      </concept>
      <concept>
        <code value="ORPHA:211266" />
        <display value="Rare arteriovenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:211277" />
        <display value="Complex vascular malformation with associated anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:2114" />
        <display value="Hip dysplasia, Beukes type" />
      </concept>
      <concept>
        <code value="ORPHA:2115" />
        <display value="Harrod syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2116" />
        <display value="Hartnup disease" />
      </concept>
      <concept>
        <code value="ORPHA:2117" />
        <display value="Hartsfield syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2118" />
        <display value="Hawkinsinuria" />
      </concept>
      <concept>
        <code value="ORPHA:2119" />
        <display value="HEC syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:212" />
        <display value="Cystathioninuria" />
      </concept>
      <concept>
        <code value="ORPHA:2122" />
        <display value="Kaposiform hemangioendothelioma" />
      </concept>
      <concept>
        <code value="ORPHA:2123" />
        <display value="Diffuse neonatal hemangiomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:2124" />
        <display value="Cavernous hemangiomas of face-supraumbilical midline raphe syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2126" />
        <display value="Solitary fibrous tumor" />
      </concept>
      <concept>
        <code value="ORPHA:2128" />
        <display value="Isolated hemihyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:213" />
        <display value="Cystinosis" />
      </concept>
      <concept>
        <code value="ORPHA:2130" />
        <display value="Hemimelia" />
      </concept>
      <concept>
        <code value="ORPHA:2131" />
        <display value="Alternating hemiplegia of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:2132" />
        <display value="Hemoglobin C disease" />
      </concept>
      <concept>
        <code value="ORPHA:2133" />
        <display value="Hemoglobin E disease" />
      </concept>
      <concept>
        <code value="ORPHA:2134" />
        <display value="Atypical hemolytic-uremic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2135" />
        <display value="Hennekam-Beemer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:213500" />
        <display value="Ovarian cancer" />
      </concept>
      <concept>
        <code value="ORPHA:213504" />
        <display value="Adenocarcinoma of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:213512" />
        <display value="Malignant mixed Mullerian tumor of the ovary" />
      </concept>
      <concept>
        <code value="ORPHA:213517" />
        <display value="Familial ovarian cancer" />
      </concept>
      <concept>
        <code value="ORPHA:213524" />
        <display value="Hereditary site-specific ovarian cancer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:213528" />
        <display value="Rare adenocarcinoma of the breast" />
      </concept>
      <concept>
        <code value="ORPHA:213531" />
        <display value="Metaplastic carcinoma of the breast" />
      </concept>
      <concept>
        <code value="ORPHA:213557" />
        <display value="Salivary gland type cancer of the breast" />
      </concept>
      <concept>
        <code value="ORPHA:213564" />
        <display value="Rare uterine cancer" />
      </concept>
      <concept>
        <code value="ORPHA:213569" />
        <display value="Rare cancer of corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213574" />
        <display value="Rare variants of adenocarcinoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213589" />
        <display value="Malignant mixed epithelial and mesenchymal tumor of corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:2136" />
        <display value="Hennekam syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:213600" />
        <display value="Adenosarcoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213605" />
        <display value="Carcinofibroma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213610" />
        <display value="Carcinosarcoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213615" />
        <display value="Rhabdomyosarcoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213620" />
        <display value="Sarcoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213625" />
        <display value="Leiomyosarcoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213630" />
        <display value="Primitive neuroectodermal tumor of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:2137" />
        <display value="Autoimmune hepatitis" />
      </concept>
      <concept>
        <code value="ORPHA:213711" />
        <display value="Endometrial stromal sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:213716" />
        <display value="Squamous cell carcinoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213721" />
        <display value="Undifferentiated carcinoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213726" />
        <display value="Papillary carcinoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213731" />
        <display value="High-grade neuroendocrine carcinoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213736" />
        <display value="Low-grade neuroendocrine tumor of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213741" />
        <display value="Adenoid cystic carcinoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213746" />
        <display value="Transitional cell carcinoma of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213751" />
        <display value="Malignant germ cell tumor of the corpus uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213761" />
        <display value="Rare cancer of cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213767" />
        <display value="Squamous cell carcinoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213772" />
        <display value="Adenocarcinoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213777" />
        <display value="High-grade neuroendocrine carcinoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213782" />
        <display value="Malignant mixed epithelial and mesenchymal tumor of cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213787" />
        <display value="Carcinosarcoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213792" />
        <display value="Adenosarcoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213797" />
        <display value="Sarcoma of cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:2138" />
        <display value="46,XX ovotesticular disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:213802" />
        <display value="Rhabdomyosarcoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213807" />
        <display value="Leiomyosarcoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213812" />
        <display value="Primitive neuroectodermal tumor of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213817" />
        <display value="Papillary carcinoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213823" />
        <display value="Adenoid cystic carcinoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213828" />
        <display value="Adenoid basal carcinoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213833" />
        <display value="Glassy cell carcinoma of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:213837" />
        <display value="Malignant germ cell tumor of the cervix uteri" />
      </concept>
      <concept>
        <code value="ORPHA:2139" />
        <display value="Hernandez-Aguirre Negrete syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:214" />
        <display value="Cystinuria" />
      </concept>
      <concept>
        <code value="ORPHA:2140" />
        <display value="Congenital diaphragmatic hernia" />
      </concept>
      <concept>
        <code value="ORPHA:2141" />
        <display value="Diaphragmatic defect-limb deficiency-skull defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2143" />
        <display value="Donnai-Barrow syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2145" />
        <display value="Craniosynostosis, Herrmann-Opitz type" />
      </concept>
      <concept>
        <code value="ORPHA:2148" />
        <display value="Lissencephaly type 1 due to doublecortin gene mutation" />
      </concept>
      <concept>
        <code value="ORPHA:2149" />
        <display value="Nodular neuronal heterotopia" />
      </concept>
      <concept>
        <code value="ORPHA:215" />
        <display value="Congenital stationary night blindness" />
      </concept>
      <concept>
        <code value="ORPHA:2150" />
        <display value="Hirschsprung disease-type D brachydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2151" />
        <display value="Hirschsprung disease-ganglioneuroblastoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2152" />
        <display value="Mowat-Wilson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2153" />
        <display value="Hirschsprung disease-nail hypoplasia-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2155" />
        <display value="Hirschsprung disease-deafness-polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2157" />
        <display value="Histidinemia" />
      </concept>
      <concept>
        <code value="ORPHA:216" />
        <display value="Neuronal ceroid lipofuscinosis" />
      </concept>
      <concept>
        <code value="ORPHA:2162" />
        <display value="Holoprosencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:2163" />
        <display value="Holoprosencephaly-craniosynostosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:216445" />
        <display value="Prelingual non-syndromic genetic deafness" />
      </concept>
      <concept>
        <code value="ORPHA:216452" />
        <display value="Postlingual non-syndromic genetic deafness" />
      </concept>
      <concept>
        <code value="ORPHA:2165" />
        <display value="Holoprosencephaly-caudal dysgenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2166" />
        <display value="Holoprosencephaly-postaxial polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:216675" />
        <display value="Transposition of the great arteries" />
      </concept>
      <concept>
        <code value="ORPHA:216694" />
        <display value="Congenitally corrected transposition of the great arteries" />
      </concept>
      <concept>
        <code value="ORPHA:2167" />
        <display value="Holzgreve syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:216718" />
        <display value="Isolated congenitally uncorrected transposition of the great arteries" />
      </concept>
      <concept>
        <code value="ORPHA:216729" />
        <display value="Congenitally uncorrected transposition of the great arteries with cardiac malformation" />
      </concept>
      <concept>
        <code value="ORPHA:216796" />
        <display value="Osteogenesis imperfecta type 1" />
      </concept>
      <concept>
        <code value="ORPHA:2168" />
        <display value="Homocarnosinosis" />
      </concept>
      <concept>
        <code value="ORPHA:216804" />
        <display value="Osteogenesis imperfecta type 2" />
      </concept>
      <concept>
        <code value="ORPHA:216812" />
        <display value="Osteogenesis imperfecta type 3" />
      </concept>
      <concept>
        <code value="ORPHA:216820" />
        <display value="Osteogenesis imperfecta type 4" />
      </concept>
      <concept>
        <code value="ORPHA:216828" />
        <display value="Osteogenesis imperfecta type 5" />
      </concept>
      <concept>
        <code value="ORPHA:216866" />
        <display value="Classic pantothenate kinase-associated neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:216873" />
        <display value="Atypical pantothenate kinase-associated neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:2169" />
        <display value="Methylcobalamin deficiency type cblE" />
      </concept>
      <concept>
        <code value="ORPHA:216972" />
        <display value="Niemann-Pick disease type C, severe perinatal form" />
      </concept>
      <concept>
        <code value="ORPHA:216975" />
        <display value="Niemann-Pick disease type C, severe early infantile neurologic onset" />
      </concept>
      <concept>
        <code value="ORPHA:216978" />
        <display value="Niemann-Pick disease type C, late infantile neurologic onset" />
      </concept>
      <concept>
        <code value="ORPHA:216981" />
        <display value="Niemann-Pick disease type C, juvenile neurologic onset" />
      </concept>
      <concept>
        <code value="ORPHA:216986" />
        <display value="Niemann-Pick disease type C, adult neurologic onset" />
      </concept>
      <concept>
        <code value="ORPHA:217" />
        <display value="Isolated Dandy-Walker malformation" />
      </concept>
      <concept>
        <code value="ORPHA:2170" />
        <display value="Methylcobalamin deficiency type cblG" />
      </concept>
      <concept>
        <code value="ORPHA:217008" />
        <display value="Bockenheimer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217012" />
        <display value="Spinocerebellar ataxia type 31" />
      </concept>
      <concept>
        <code value="ORPHA:217017" />
        <display value="Zechi-Ceide syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217023" />
        <display value="Atypical hemolytic-uremic syndrome with thrombomodulin anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:217026" />
        <display value="Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type" />
      </concept>
      <concept>
        <code value="ORPHA:217055" />
        <display value="Autosomal recessive intermediate Charcot-Marie-Tooth disease type A" />
      </concept>
      <concept>
        <code value="ORPHA:217059" />
        <display value="Isolated congenital digital clubbing" />
      </concept>
      <concept>
        <code value="ORPHA:217064" />
        <display value="5-fluorouracil poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:217071" />
        <display value="Renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:217074" />
        <display value="Rare carcinoma of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:217085" />
        <display value="Mucopolysaccharidosis type 2, severe form" />
      </concept>
      <concept>
        <code value="ORPHA:217093" />
        <display value="Mucopolysaccharidosis type 2, attenuated form" />
      </concept>
      <concept>
        <code value="ORPHA:2172" />
        <display value="Microcephaly-glomerulonephritis-marfanoid habitus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217253" />
        <display value="Limbic encephalitis with NMDA receptor antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:217260" />
        <display value="Progressive multifocal leukoencephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217266" />
        <display value="BNAR syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217330" />
        <display value="REN-related autosomal dominant tubulointerstitial kidney disease" />
      </concept>
      <concept>
        <code value="ORPHA:217335" />
        <display value="RIN2 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217340" />
        <display value="17q21.31 microduplication  syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217346" />
        <display value="19q13.11 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217371" />
        <display value="Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins" />
      </concept>
      <concept>
        <code value="ORPHA:217377" />
        <display value="Microduplication Xp11.22-p11.23 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217382" />
        <display value="Neurodegenerative syndrome due to cerebral folate transport deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:217385" />
        <display value="17p13.3 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:217390" />
        <display value="Combined immunodeficiency due to DOCK8 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:217396" />
        <display value="Progressive polyneuropathy with bilateral striatal necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:217399" />
        <display value="Congenital insensitivity to pain with hyperhidrosis" />
      </concept>
      <concept>
        <code value="ORPHA:217407" />
        <display value="Hereditary hypotrichosis with recurrent skin vesicles" />
      </concept>
      <concept>
        <code value="ORPHA:217454" />
        <display value="Rare hereditary thrombophilia" />
      </concept>
      <concept>
        <code value="ORPHA:217467" />
        <display value="Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:217557" />
        <display value="Pulmonary interstitial glycogenosis" />
      </concept>
      <concept>
        <code value="ORPHA:217560" />
        <display value="Neuroendocrine cell hyperplasia of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:217563" />
        <display value="Neonatal acute respiratory distress due to SP-B deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:217566" />
        <display value="Chronic respiratory distress with surfactant metabolism deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:217569" />
        <display value="Hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217572" />
        <display value="Glycogen storage disease with hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217581" />
        <display value="Lysosomal disease with hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217587" />
        <display value="Mitochondrial disease with hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217591" />
        <display value="Fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217595" />
        <display value="Syndrome associated with hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217598" />
        <display value="Non-familial hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2176" />
        <display value="Infantile systemic hyalinosis" />
      </concept>
      <concept>
        <code value="ORPHA:217601" />
        <display value="Hypertrophic cardiomyopathy due to intensive athletic training" />
      </concept>
      <concept>
        <code value="ORPHA:217604" />
        <display value="Dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217607" />
        <display value="Familial dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217610" />
        <display value="Neuromuscular disease with dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217613" />
        <display value="Mitochondrial disease with dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217616" />
        <display value="Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217619" />
        <display value="Syndrome associated with dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217622" />
        <display value="Sensorineural deafness with dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217629" />
        <display value="Non-familial dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217632" />
        <display value="Restrictive cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217635" />
        <display value="Familial restrictive cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217638" />
        <display value="Lysosomal disease with restrictive cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:217656" />
        <display value="Familial isolated arrhythmogenic right ventricular dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:217678" />
        <display value="Unclassified cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2177" />
        <display value="Hydranencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:217720" />
        <display value="Non-familial restrictive cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:218" />
        <display value="Darier disease" />
      </concept>
      <concept>
        <code value="ORPHA:2180" />
        <display value="Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2181" />
        <display value="Hydrocephaly-tall stature-joint laxity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2182" />
        <display value="Hydrocephalus with stenosis of the aqueduct of Sylvius" />
      </concept>
      <concept>
        <code value="ORPHA:2183" />
        <display value="Hydrocephalus-obesity-hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:218436" />
        <display value="Rare cardiac rhythm disease" />
      </concept>
      <concept>
        <code value="ORPHA:218439" />
        <display value="Non-genetic cardiac rhythm disease" />
      </concept>
      <concept>
        <code value="ORPHA:2185" />
        <display value="Congenital hydrocephalus" />
      </concept>
      <concept>
        <code value="ORPHA:2186" />
        <display value="Hydrocephalus-blue sclerae-nephropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2189" />
        <display value="Hydrolethalus" />
      </concept>
      <concept>
        <code value="ORPHA:219" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2F" />
      </concept>
      <concept>
        <code value="ORPHA:2190" />
        <display value="Congenital hydronephrosis" />
      </concept>
      <concept>
        <code value="ORPHA:2194" />
        <display value="Anti-HLA hyperimmunization" />
      </concept>
      <concept>
        <code value="ORPHA:2195" />
        <display value="Dicarboxylic aminoaciduria" />
      </concept>
      <concept>
        <code value="ORPHA:2196" />
        <display value="Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement" />
      </concept>
      <concept>
        <code value="ORPHA:2197" />
        <display value="Idiopathic hypercalciuria" />
      </concept>
      <concept>
        <code value="ORPHA:2198" />
        <display value="Palmoplantar keratoderma-esophageal carcinoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2199" />
        <display value="Epidermolytic palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:22" />
        <display value="Succinic semialdehyde dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:220" />
        <display value="Denys-Drash syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2200" />
        <display value="Focal palmoplantar and gingival keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:2201" />
        <display value="Palmoplantar keratoderma-spastic paralysis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2202" />
        <display value="Palmoplantar keratoderma-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:220295" />
        <display value="Xeroderma pigmentosum-Cockayne syndrome complex" />
      </concept>
      <concept>
        <code value="ORPHA:2203" />
        <display value="Hyperlysinemia" />
      </concept>
      <concept>
        <code value="ORPHA:220386" />
        <display value="Semilobar holoprosencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:220393" />
        <display value="Diffuse cutaneous systemic sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:2204" />
        <display value="Dysplastic cortical hyperostosis" />
      </concept>
      <concept>
        <code value="ORPHA:220402" />
        <display value="Limited cutaneous systemic sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:220407" />
        <display value="Limited systemic sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:220436" />
        <display value="Quebec platelet disorder" />
      </concept>
      <concept>
        <code value="ORPHA:220443" />
        <display value="Bleeding diathesis due to thromboxane synthesis deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:220448" />
        <display value="Macrothrombocytopenia with mitral valve insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:220452" />
        <display value="Isolated hereditary giant platelet disorder" />
      </concept>
      <concept>
        <code value="ORPHA:220460" />
        <display value="Attenuated familial adenomatous polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:220465" />
        <display value="Laron syndrome with immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:220489" />
        <display value="Rare hereditary hemochromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:220493" />
        <display value="Joubert syndrome with ocular defect" />
      </concept>
      <concept>
        <code value="ORPHA:220497" />
        <display value="Joubert syndrome with renal defect" />
      </concept>
      <concept>
        <code value="ORPHA:2206" />
        <display value="Ankylosing vertebral hyperostosis with tylosis" />
      </concept>
      <concept>
        <code value="ORPHA:2207" />
        <display value="Familial primary hyperparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:2209" />
        <display value="Maternal phenylketonuria" />
      </concept>
      <concept>
        <code value="ORPHA:221" />
        <display value="Dermatomyositis" />
      </concept>
      <concept>
        <code value="ORPHA:221008" />
        <display value="Rothmund-Thomson syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:221016" />
        <display value="Rothmund-Thomson syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:221039" />
        <display value="Hereditary sclerosing poikiloderma, Weary type" />
      </concept>
      <concept>
        <code value="ORPHA:221043" />
        <display value="Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:221046" />
        <display value="Poikiloderma with neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:221054" />
        <display value="Acrocephalopolydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:221061" />
        <display value="Familial cerebral cavernous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:221074" />
        <display value="Marchiafava-Bignami disease" />
      </concept>
      <concept>
        <code value="ORPHA:221078" />
        <display value="Combined hyperactive dysfunction syndrome of the cranial nerves" />
      </concept>
      <concept>
        <code value="ORPHA:221083" />
        <display value="Hemifacial spasm" />
      </concept>
      <concept>
        <code value="ORPHA:221091" />
        <display value="Trigeminal neuralgia" />
      </concept>
      <concept>
        <code value="ORPHA:221098" />
        <display value="Glossopharyngeal neuralgia" />
      </concept>
      <concept>
        <code value="ORPHA:2211" />
        <display value="Hypertelorism-hypospadias-polysyndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:221106" />
        <display value="Isolated facial myokymia" />
      </concept>
      <concept>
        <code value="ORPHA:221109" />
        <display value="Cranial neuralgia" />
      </concept>
      <concept>
        <code value="ORPHA:221114" />
        <display value="Acquired peripheral movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:221117" />
        <display value="Gerstmann syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:221120" />
        <display value="Pseudoaminopterin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:221126" />
        <display value="Fowler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:221139" />
        <display value="Combined immunodeficiency with faciooculoskeletal anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:221142" />
        <display value="Confetti-like macular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:221145" />
        <display value="Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:221150" />
        <display value="Pitt-Hopkins-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2213" />
        <display value="Hypertelorism-microtia-facial clefting syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2215" />
        <display value="Multiple pterygium-malignant hyperthermia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2216" />
        <display value="Maternal hyperthermia-induced birth defects" />
      </concept>
      <concept>
        <code value="ORPHA:2218" />
        <display value="Cervical hypertrichosis-peripheral neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:222" />
        <display value="Erosive pustular dermatosis of the scalp" />
      </concept>
      <concept>
        <code value="ORPHA:2220" />
        <display value="Hypertrichosis cubiti" />
      </concept>
      <concept>
        <code value="ORPHA:2221" />
        <display value="Acquired hypertrichosis lanuginosa" />
      </concept>
      <concept>
        <code value="ORPHA:2222" />
        <display value="Hypertrichosis lanuginosa congenita" />
      </concept>
      <concept>
        <code value="ORPHA:2224" />
        <display value="Hypertryptophanemia" />
      </concept>
      <concept>
        <code value="ORPHA:222628" />
        <display value="Hereditary poikiloderma" />
      </concept>
      <concept>
        <code value="ORPHA:2228" />
        <display value="Hypodontia-dysplasia of nails syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2229" />
        <display value="Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:223" />
        <display value="Nephrogenic diabetes insipidus" />
      </concept>
      <concept>
        <code value="ORPHA:2230" />
        <display value="Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2232" />
        <display value="Primary hypergonadotropic hypogonadism-partial alopecia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2233" />
        <display value="Hypogonadism-mitral valve prolapse-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2234" />
        <display value="Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2235" />
        <display value="Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2237" />
        <display value="Hypoparathyroidism-sensorineural deafness-renal disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:223713" />
        <display value="Mitochondrial oxidative phosphorylation disorder" />
      </concept>
      <concept>
        <code value="ORPHA:223727" />
        <display value="Bone sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:223735" />
        <display value="Lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:2238" />
        <display value="Familial isolated hypoparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:2239" />
        <display value="Familial isolated hypoparathyroidism due to agenesis of parathyroid gland" />
      </concept>
      <concept>
        <code value="ORPHA:224" />
        <display value="Neonatal diabetes mellitus" />
      </concept>
      <concept>
        <code value="ORPHA:2241" />
        <display value="Megacystis-microcolon-intestinal hypoperistalsis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2246" />
        <display value="Cerebellar hypoplasia-tapetoretinal degeneration syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2248" />
        <display value="Hypoplastic left heart syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2249" />
        <display value="Ulna hypoplasia-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:225" />
        <display value="Maternally-inherited diabetes and deafness" />
      </concept>
      <concept>
        <code value="ORPHA:2250" />
        <display value="Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2251" />
        <display value="Thumb deformity-alopecia-pigmentation anomaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:225123" />
        <display value="Hemochromatosis type 3" />
      </concept>
      <concept>
        <code value="ORPHA:225147" />
        <display value="Sporadic infantile bilateral striatal necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:225154" />
        <display value="Familial infantile bilateral striatal necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:2252" />
        <display value="Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2253" />
        <display value="Foveal hypoplasia-presenile cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2254" />
        <display value="Pontocerebellar hypoplasia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:2255" />
        <display value="Pancreatic hypoplasia-diabetes-congenital heart disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2256" />
        <display value="Fibulo-ulnar hypoplasia-renal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:225681" />
        <display value="Lysosomal disease with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:225686" />
        <display value="Peroxisomal disease with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:225689" />
        <display value="Amino acid or protein metabolism disease with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:225692" />
        <display value="Metal transport or utilization disorder with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:225696" />
        <display value="Energy metabolism disorder with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:2257" />
        <display value="Primary pulmonary hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:225700" />
        <display value="Mitochondrial disease with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:225703" />
        <display value="Mitochondrial disease with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:225707" />
        <display value="Metabolic neurotransmission anomaly with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:225710" />
        <display value="Sterol metabolism disorder with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:225713" />
        <display value="Other metabolic disease with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:226" />
        <display value="Dihydropteridine reductase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2260" />
        <display value="Oligomeganephronia" />
      </concept>
      <concept>
        <code value="ORPHA:2261" />
        <display value="Hypospadias-intellectual disability, Goldblatt type syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:226292" />
        <display value="Permanent congenital hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:226295" />
        <display value="Primary congenital hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:226298" />
        <display value="Central congenital hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:226307" />
        <display value="Hypothyroidism due to deficient transcription factors involved in pituitary development or function" />
      </concept>
      <concept>
        <code value="ORPHA:226310" />
        <display value="Peripheral hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:226313" />
        <display value="Congenital hypothyroidism due to maternal intake of antithyroid drugs" />
      </concept>
      <concept>
        <code value="ORPHA:226316" />
        <display value="Genetic transient congenital hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:2266" />
        <display value="Hypotrichosis-intellectual disability, Lopes type" />
      </concept>
      <concept>
        <code value="ORPHA:2268" />
        <display value="ICF syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2269" />
        <display value="Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:227" />
        <display value="Diphallia" />
      </concept>
      <concept>
        <code value="ORPHA:2271" />
        <display value="Congenital ichthyosis-microcephalus-tetraplegia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2272" />
        <display value="Ichthyosis-oral and digital anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2273" />
        <display value="Ichthyosis follicularis-alopecia-photophobia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2274" />
        <display value="Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:227510" />
        <display value="Multiple system atrophy, cerebellar type" />
      </concept>
      <concept>
        <code value="ORPHA:227535" />
        <display value="Hereditary breast cancer" />
      </concept>
      <concept>
        <code value="ORPHA:227796" />
        <display value="Fundus albipunctatus" />
      </concept>
      <concept>
        <code value="ORPHA:2278" />
        <display value="Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:227972" />
        <display value="Toxic oil syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:227976" />
        <display value="Autosomal recessive optic atrophy, OPA7 type" />
      </concept>
      <concept>
        <code value="ORPHA:227982" />
        <display value="Autoimmune polyendocrinopathy type 3" />
      </concept>
      <concept>
        <code value="ORPHA:227990" />
        <display value="Autoimmune polyendocrinopathy type 4" />
      </concept>
      <concept>
        <code value="ORPHA:228000" />
        <display value="Idiopathic CD4 lymphocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:228003" />
        <display value="Severe combined immunodeficiency due to CORO1A deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:228012" />
        <display value="Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228116" />
        <display value="Hughes-Stovin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228119" />
        <display value="Fusariosis" />
      </concept>
      <concept>
        <code value="ORPHA:228123" />
        <display value="Coccidioidomycosis" />
      </concept>
      <concept>
        <code value="ORPHA:228140" />
        <display value="Idiopathic ventricular fibrillation, non Brugada type" />
      </concept>
      <concept>
        <code value="ORPHA:228145" />
        <display value="Multiple sclerosis variant" />
      </concept>
      <concept>
        <code value="ORPHA:228157" />
        <display value="Marburg acute multiple sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:228165" />
        <display value="Balo concentric sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:228169" />
        <display value="Autosomal dominant striatal neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:228174" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2N" />
      </concept>
      <concept>
        <code value="ORPHA:228179" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2M" />
      </concept>
      <concept>
        <code value="ORPHA:228184" />
        <display value="Heart-hand syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228190" />
        <display value="Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2282" />
        <display value="Dysmorphism-short stature-deafness-disorder of sex development syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228215" />
        <display value="Genetic dermis elastic tissue disorder" />
      </concept>
      <concept>
        <code value="ORPHA:228218" />
        <display value="Acquired dermis elastic tissue disorder" />
      </concept>
      <concept>
        <code value="ORPHA:228221" />
        <display value="Acquired dermis elastic tissue disorder with decreased elastic tissue" />
      </concept>
      <concept>
        <code value="ORPHA:228224" />
        <display value="Acquired dermis elastic tissue disorder with increased elastic tissue" />
      </concept>
      <concept>
        <code value="ORPHA:228227" />
        <display value="Late-onset focal dermal elastosis" />
      </concept>
      <concept>
        <code value="ORPHA:228236" />
        <display value="Linear focal elastosis" />
      </concept>
      <concept>
        <code value="ORPHA:228240" />
        <display value="Elastoderma" />
      </concept>
      <concept>
        <code value="ORPHA:228243" />
        <display value="Elastofibroma dorsi" />
      </concept>
      <concept>
        <code value="ORPHA:228247" />
        <display value="Acquired pseudoxanthoma elasticum" />
      </concept>
      <concept>
        <code value="ORPHA:228254" />
        <display value="Elastoma" />
      </concept>
      <concept>
        <code value="ORPHA:228264" />
        <display value="Papular elastorrhexis" />
      </concept>
      <concept>
        <code value="ORPHA:228272" />
        <display value="Primary anetoderma" />
      </concept>
      <concept>
        <code value="ORPHA:228277" />
        <display value="Familial anetoderma" />
      </concept>
      <concept>
        <code value="ORPHA:228285" />
        <display value="Acquired cutis laxa" />
      </concept>
      <concept>
        <code value="ORPHA:228290" />
        <display value="White fibrous papulosis of the neck" />
      </concept>
      <concept>
        <code value="ORPHA:228293" />
        <display value="Pseudoxanthoma elasticum-like papillary dermal elastolysis" />
      </concept>
      <concept>
        <code value="ORPHA:228299" />
        <display value="Mid-dermal elastolysis" />
      </concept>
      <concept>
        <code value="ORPHA:228302" />
        <display value="Carnitine palmitoyl transferase II deficiency, myopathic form" />
      </concept>
      <concept>
        <code value="ORPHA:228305" />
        <display value="Carnitine palmitoyl transferase II deficiency, severe infantile form" />
      </concept>
      <concept>
        <code value="ORPHA:228308" />
        <display value="Carnitine palmitoyl transferase II deficiency, neonatal form" />
      </concept>
      <concept>
        <code value="ORPHA:228312" />
        <display value="Autoimmune hemolytic anemia, cold type" />
      </concept>
      <concept>
        <code value="ORPHA:228315" />
        <display value="Idiopathic hypersomnia with long sleep time" />
      </concept>
      <concept>
        <code value="ORPHA:228318" />
        <display value="Idiopathic hypersomnia without long sleep time" />
      </concept>
      <concept>
        <code value="ORPHA:228329" />
        <display value="CLN1 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228337" />
        <display value="CLN10 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228340" />
        <display value="CLN4A disease" />
      </concept>
      <concept>
        <code value="ORPHA:228343" />
        <display value="CLN4B disease" />
      </concept>
      <concept>
        <code value="ORPHA:228346" />
        <display value="CLN3 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228349" />
        <display value="CLN2 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228354" />
        <display value="CLN8 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228357" />
        <display value="CLN9 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228360" />
        <display value="CLN5 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228363" />
        <display value="CLN6 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228366" />
        <display value="CLN7 disease" />
      </concept>
      <concept>
        <code value="ORPHA:228371" />
        <display value="Foodborne botulism" />
      </concept>
      <concept>
        <code value="ORPHA:228374" />
        <display value="Charcot-Marie-Tooth disease type 2B5" />
      </concept>
      <concept>
        <code value="ORPHA:228379" />
        <display value="Virus-associated trichodysplasia spinulosa" />
      </concept>
      <concept>
        <code value="ORPHA:228384" />
        <display value="5q14.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228387" />
        <display value="Spondylo-megaepiphyseal-metaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:228390" />
        <display value="Frontonasal dysplasia-alopecia-genital anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228396" />
        <display value="Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228399" />
        <display value="8q12 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228402" />
        <display value="2q23.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228410" />
        <display value="Polyvalvular heart disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228415" />
        <display value="5q35 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:228423" />
        <display value="Monocytopenia with susceptibility to infections" />
      </concept>
      <concept>
        <code value="ORPHA:228426" />
        <display value="Syndromic multisystem autoimmune disease due to Itch deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2285" />
        <display value="Primary basilar invagination" />
      </concept>
      <concept>
        <code value="ORPHA:2286" />
        <display value="Solitary median maxillary central incisor syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2287" />
        <display value="Fused mandibular incisors" />
      </concept>
      <concept>
        <code value="ORPHA:2289" />
        <display value="Neuronal intranuclear inclusion disease" />
      </concept>
      <concept>
        <code value="ORPHA:229" />
        <display value="Familial aortic dissection" />
      </concept>
      <concept>
        <code value="ORPHA:2290" />
        <display value="Microvillus inclusion disease" />
      </concept>
      <concept>
        <code value="ORPHA:2291" />
        <display value="Congenital velopharyngeal incompetence" />
      </concept>
      <concept>
        <code value="ORPHA:2292" />
        <display value="Congenital bowing of long bones" />
      </concept>
      <concept>
        <code value="ORPHA:2295" />
        <display value="Familial articular hypermobility syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2297" />
        <display value="Insulin-resistance syndrome type A" />
      </concept>
      <concept>
        <code value="ORPHA:229717" />
        <display value="Isolated agammaglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:229720" />
        <display value="Syndromic agammaglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:2298" />
        <display value="Insulin-resistance syndrome type B" />
      </concept>
      <concept>
        <code value="ORPHA:2299" />
        <display value="Aortic arch interruption" />
      </concept>
      <concept>
        <code value="ORPHA:23" />
        <display value="Argininosuccinic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:230" />
        <display value="Dopamine beta-hydroxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2300" />
        <display value="Multiple intestinal atresia" />
      </concept>
      <concept>
        <code value="ORPHA:2301" />
        <display value="Congenital short bowel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2302" />
        <display value="Asbestos intoxication" />
      </concept>
      <concept>
        <code value="ORPHA:2305" />
        <display value="Isotretinoin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2306" />
        <display value="Isotretinoin-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2307" />
        <display value="IVIC syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2308" />
        <display value="Jacobsen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:230800" />
        <display value="Toxin-mediated infectious botulism" />
      </concept>
      <concept>
        <code value="ORPHA:230839" />
        <display value="Ehlers-Danlos syndrome due to tenascin-X deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:230845" />
        <display value="Ehlers-Danlos syndrome, vascular-like type" />
      </concept>
      <concept>
        <code value="ORPHA:230851" />
        <display value="Ehlers-Danlos syndrome, cardiac valvular type" />
      </concept>
      <concept>
        <code value="ORPHA:230857" />
        <display value="Ehlers-Danlos/osteogenesis imperfecta syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2309" />
        <display value="Pachyonychia congenita" />
      </concept>
      <concept>
        <code value="ORPHA:231" />
        <display value="Dracunculiasis" />
      </concept>
      <concept>
        <code value="ORPHA:2310" />
        <display value="Absence deformity of leg-cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231013" />
        <display value="Congenital trigeminal anesthesia" />
      </concept>
      <concept>
        <code value="ORPHA:231031" />
        <display value="Erythema palmare hereditarium" />
      </concept>
      <concept>
        <code value="ORPHA:231040" />
        <display value="Familial generalized lentiginosis" />
      </concept>
      <concept>
        <code value="ORPHA:2311" />
        <display value="Autosomal recessive spondylocostal dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:231108" />
        <display value="Familial rhabdoid tumor" />
      </concept>
      <concept>
        <code value="ORPHA:231111" />
        <display value="Drug-induced lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:231117" />
        <display value="Beckwith-Wiedemann syndrome due to imprinting defect of 11p15" />
      </concept>
      <concept>
        <code value="ORPHA:231120" />
        <display value="Beckwith-Wiedemann syndrome due to CDKN1C mutation" />
      </concept>
      <concept>
        <code value="ORPHA:231127" />
        <display value="Beckwith-Wiedemann syndrome due to 11p15 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:231130" />
        <display value="Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion" />
      </concept>
      <concept>
        <code value="ORPHA:231137" />
        <display value="Silver-Russell syndrome due to 7p11.2p13 microduplication" />
      </concept>
      <concept>
        <code value="ORPHA:231140" />
        <display value="Silver-Russell syndrome due to an imprinting defect of 11p15" />
      </concept>
      <concept>
        <code value="ORPHA:231144" />
        <display value="Silver-Russell syndrome due to 11p15 microduplication" />
      </concept>
      <concept>
        <code value="ORPHA:231147" />
        <display value="Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11" />
      </concept>
      <concept>
        <code value="ORPHA:231154" />
        <display value="Combined immunodeficiency due to partial RAG1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:231160" />
        <display value="Familial cerebral saccular aneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:231169" />
        <display value="Usher syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:231178" />
        <display value="Usher syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:231183" />
        <display value="Usher syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:2312" />
        <display value="Transient familial neonatal hyperbilirubinemia" />
      </concept>
      <concept>
        <code value="ORPHA:231214" />
        <display value="Beta-thalassemia major" />
      </concept>
      <concept>
        <code value="ORPHA:231222" />
        <display value="Beta-thalassemia intermedia" />
      </concept>
      <concept>
        <code value="ORPHA:231226" />
        <display value="Dominant beta-thalassemia" />
      </concept>
      <concept>
        <code value="ORPHA:231230" />
        <display value="Beta-thalassemia associated with another hemoglobin anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:231237" />
        <display value="Delta-beta-thalassemia" />
      </concept>
      <concept>
        <code value="ORPHA:231242" />
        <display value="Hemoglobin C-beta-thalassemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231249" />
        <display value="Hemoglobin E-beta-thalassemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231386" />
        <display value="Beta-thalassemia with other manifestations" />
      </concept>
      <concept>
        <code value="ORPHA:231393" />
        <display value="Beta-thalassemia-X-linked thrombocytopenia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2314" />
        <display value="Autosomal dominant hyper-IgE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231401" />
        <display value="Alpha-thalassemia-myelodysplastic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231413" />
        <display value="Variant of Guillain-Barre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231416" />
        <display value="Regional variant of Guillain-Barre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231419" />
        <display value="Functional variant of Guillain-Barre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231426" />
        <display value="Pharyngeal-cervical-brachial variant of Guillain-Barre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231445" />
        <display value="Paraparetic variant of Guillain-Barre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231450" />
        <display value="Acute pure sensory neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:231457" />
        <display value="Acute pandysautonomia" />
      </concept>
      <concept>
        <code value="ORPHA:231466" />
        <display value="Acute sensory ataxic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:2315" />
        <display value="Johanson-Blizzard syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231500" />
        <display value="Hermansky-Pudlak syndrome with pulmonary fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:231512" />
        <display value="Hermansky-Pudlak syndrome without pulmonary fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:231531" />
        <display value="Hermansky-Pudlak syndrome type 7" />
      </concept>
      <concept>
        <code value="ORPHA:231537" />
        <display value="Hermansky-Pudlak syndrome type 8" />
      </concept>
      <concept>
        <code value="ORPHA:231556" />
        <display value="Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231568" />
        <display value="Generalized dominant dystrophic epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:231573" />
        <display value="Congenital erosive and vesicular dermatosis" />
      </concept>
      <concept>
        <code value="ORPHA:231580" />
        <display value="Primary unilateral adrenal hyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2316" />
        <display value="Johnson neuroectodermal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231625" />
        <display value="Adrenocortical carcinoma with pure aldosterone hypersecretion" />
      </concept>
      <concept>
        <code value="ORPHA:231632" />
        <display value="Ectopic aldosterone-producing tumor" />
      </concept>
      <concept>
        <code value="ORPHA:231637" />
        <display value="Rare surgically correctable form of primary aldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:231641" />
        <display value="Rare non surgically correctable form of primary aldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:231662" />
        <display value="Isolated growth hormone deficiency type IA" />
      </concept>
      <concept>
        <code value="ORPHA:231671" />
        <display value="Isolated growth hormone deficiency type IB" />
      </concept>
      <concept>
        <code value="ORPHA:231679" />
        <display value="Isolated growth hormone deficiency type II" />
      </concept>
      <concept>
        <code value="ORPHA:231692" />
        <display value="Isolated growth hormone deficiency type III" />
      </concept>
      <concept>
        <code value="ORPHA:231720" />
        <display value="Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231736" />
        <display value="Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:231742" />
        <display value="Epibulbar lipodermoid-preauricular appendage-polythelia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2318" />
        <display value="Joubert syndrome with oculorenal defect" />
      </concept>
      <concept>
        <code value="ORPHA:2319" />
        <display value="Juberg-Hayward syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:232" />
        <display value="Sickle cell anemia" />
      </concept>
      <concept>
        <code value="ORPHA:232035" />
        <display value="Infectious embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2322" />
        <display value="Kabuki syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:232288" />
        <display value="Alpha-thalassemia-related diseases" />
      </concept>
      <concept>
        <code value="ORPHA:2323" />
        <display value="Sanjad-Sakati syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2324" />
        <display value="Osteopenia-intellectual disability-sparse hair syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2325" />
        <display value="Epidermolysis bullosa simplex with anodontia/hypodontia" />
      </concept>
      <concept>
        <code value="ORPHA:2326" />
        <display value="Kallmann syndrome-heart disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2328" />
        <display value="Kapur-Toriello syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2329" />
        <display value="Karsch-Neugebauer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:233" />
        <display value="Duane retraction syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2330" />
        <display value="Kasabach-Merritt syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2331" />
        <display value="Kawasaki disease" />
      </concept>
      <concept>
        <code value="ORPHA:2332" />
        <display value="KBG syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2333" />
        <display value="Kenny-Caffey syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2334" />
        <display value="Autosomal dominant keratitis" />
      </concept>
      <concept>
        <code value="ORPHA:233655" />
        <display value="Rare genetic vascular disease" />
      </concept>
      <concept>
        <code value="ORPHA:2337" />
        <display value="Non-epidermolytic palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:2338" />
        <display value="Isolated punctate palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:2339" />
        <display value="Keratosis follicularis-dwarfism-cerebral atrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:234" />
        <display value="Dubin-Johnson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2340" />
        <display value="Keratosis follicularis spinulosa decalvans" />
      </concept>
      <concept>
        <code value="ORPHA:2342" />
        <display value="Haim-Munk syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2343" />
        <display value="Isolated cloverleaf skull syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2345" />
        <display value="Isolated Klippel-Feil syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2346" />
        <display value="Angioosteohypertrophic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2347" />
        <display value="Lethal Kniest-like dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2348" />
        <display value="Familial partial lipodystrophy, Dunnigan type" />
      </concept>
      <concept>
        <code value="ORPHA:2349" />
        <display value="Muscular pseudohypertrophy-hypothyroidism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:235" />
        <display value="Dubowitz syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2351" />
        <display value="Kousseff syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2353" />
        <display value="Schilbach-Rott syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2356" />
        <display value="Arachnoid cyst" />
      </concept>
      <concept>
        <code value="ORPHA:2357" />
        <display value="Bronchogenic cyst" />
      </concept>
      <concept>
        <code value="ORPHA:235832" />
        <display value="Congenital vascular bone syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:235936" />
        <display value="Familial hyperaldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:236" />
        <display value="Trisomy 9p" />
      </concept>
      <concept>
        <code value="ORPHA:2363" />
        <display value="Lacrimoauriculodentodigital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2364" />
        <display value="Glycogen storage disease due to lactate dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2368" />
        <display value="Gastroschisis" />
      </concept>
      <concept>
        <code value="ORPHA:2369" />
        <display value="Limb body wall complex" />
      </concept>
      <concept>
        <code value="ORPHA:237" />
        <display value="Duplication of urethra" />
      </concept>
      <concept>
        <code value="ORPHA:2370" />
        <display value="Larsen-like osseous dysplasia-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2371" />
        <display value="Lethal Larsen-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2372" />
        <display value="Laryngocele" />
      </concept>
      <concept>
        <code value="ORPHA:2373" />
        <display value="Congenital laryngomalacia" />
      </concept>
      <concept>
        <code value="ORPHA:2374" />
        <display value="Congenital laryngeal web" />
      </concept>
      <concept>
        <code value="ORPHA:2375" />
        <display value="Laryngeal abductor paralysis-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2377" />
        <display value="Laurence-Moon syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2378" />
        <display value="Laurin-Sandrow syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2379" />
        <display value="Early-onset parkinsonism-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238" />
        <display value="Digestive duplication" />
      </concept>
      <concept>
        <code value="ORPHA:2380" />
        <display value="Legg-Calve-Perthes disease" />
      </concept>
      <concept>
        <code value="ORPHA:2382" />
        <display value="Lennox-Gastaut syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238269" />
        <display value="AApoAII amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:238305" />
        <display value="Infundibulo-neurohypophysitis" />
      </concept>
      <concept>
        <code value="ORPHA:238329" />
        <display value="Severe X-linked mitochondrial encephalomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:238446" />
        <display value="15q11q13 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238455" />
        <display value="Infantile dystonia-parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:238459" />
        <display value="SLC35A1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:238468" />
        <display value="Hypohidrotic ectodermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:238475" />
        <display value="Familial hypercholanemia" />
      </concept>
      <concept>
        <code value="ORPHA:238505" />
        <display value="Autosomal recessive lymphoproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:238510" />
        <display value="Lymphoproliferative syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238517" />
        <display value="Hypotonia-cystinuria type 1 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238523" />
        <display value="Atypical hypotonia-cystinuria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238536" />
        <display value="Congenital secondary polycythemia" />
      </concept>
      <concept>
        <code value="ORPHA:238547" />
        <display value="Acquired secondary polycythemia" />
      </concept>
      <concept>
        <code value="ORPHA:238557" />
        <display value="Chuvash erythrocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:238569" />
        <display value="Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238578" />
        <display value="Familial clubfoot due to 17q23.1q23.2 microduplication" />
      </concept>
      <concept>
        <code value="ORPHA:238583" />
        <display value="Hyperphenylalaninemia due to tetrahydrobiopterin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:238593" />
        <display value="IgG4-related mesenteritis" />
      </concept>
      <concept>
        <code value="ORPHA:2386" />
        <display value="Leukoencephalopathy-palmoplantar keratoderma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238606" />
        <display value="Primary orthostatic tremor" />
      </concept>
      <concept>
        <code value="ORPHA:238613" />
        <display value="Beckwith-Wiedemann syndrome due to NSD1 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:238624" />
        <display value="Idiopathic intracranial hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:238637" />
        <display value="Megacystis-megaureter syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238642" />
        <display value="Primary megaureter, adult-onset form" />
      </concept>
      <concept>
        <code value="ORPHA:238646" />
        <display value="Congenital primary megaureter, obstructed form" />
      </concept>
      <concept>
        <code value="ORPHA:238650" />
        <display value="Congenital primary megaureter, refluxing form" />
      </concept>
      <concept>
        <code value="ORPHA:238654" />
        <display value="Congenital primary megaureter, nonrefluxing and unobstructed form" />
      </concept>
      <concept>
        <code value="ORPHA:238666" />
        <display value="Isolated congenital hypogonadotropic hypogonadism" />
      </concept>
      <concept>
        <code value="ORPHA:238670" />
        <display value="Isolated thyrotropin-releasing hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:238688" />
        <display value="Neonatal iodine exposure" />
      </concept>
      <concept>
        <code value="ORPHA:238696" />
        <display value="Transient congenital hypothyroidism due to maternal factor" />
      </concept>
      <concept>
        <code value="ORPHA:238699" />
        <display value="Transient congenital hypothyroidism due to neonatal factor" />
      </concept>
      <concept>
        <code value="ORPHA:2387" />
        <display value="Leukonychia totalis" />
      </concept>
      <concept>
        <code value="ORPHA:238722" />
        <display value="Familial congenital mirror movements" />
      </concept>
      <concept>
        <code value="ORPHA:238744" />
        <display value="Mammary-digital-nail syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238750" />
        <display value="4q21 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:238755" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy type 1H" />
      </concept>
      <concept>
        <code value="ORPHA:238763" />
        <display value="Glaucoma secondary to spherophakia/ectopia lentis and megalocornea" />
      </concept>
      <concept>
        <code value="ORPHA:238769" />
        <display value="1q44 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2388" />
        <display value="Choreoacanthocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:239" />
        <display value="Dyggve-Melchior-Clausen disease" />
      </concept>
      <concept>
        <code value="ORPHA:2390" />
        <display value="Lichtenstein syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2391" />
        <display value="Congenitally short costocoracoid ligament" />
      </concept>
      <concept>
        <code value="ORPHA:2394" />
        <display value="Pyruvate dehydrogenase E3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2396" />
        <display value="Encephalocraniocutaneous lipomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:2398" />
        <display value="Multiple symmetric lipomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:2399" />
        <display value="Nasopalpebral lipoma-coloboma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:24" />
        <display value="Fumaric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:240" />
        <display value="Leri-Weill dyschondrosteosis" />
      </concept>
      <concept>
        <code value="ORPHA:2400" />
        <display value="Peripheral motor neuropathy-dysautonomia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:240071" />
        <display value="Classic progressive supranuclear palsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:240085" />
        <display value="Progressive supranuclear palsy-parkinsonism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:240094" />
        <display value="Progressive supranuclear palsy-pure akinesia with gait freezing syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:240103" />
        <display value="Progressive supranuclear palsy-corticobasal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:240112" />
        <display value="Progressive supranuclear palsy-progressive non-fluent aphasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:240371" />
        <display value="Syndromic obesity" />
      </concept>
      <concept>
        <code value="ORPHA:2404" />
        <display value="Loiasis" />
      </concept>
      <concept>
        <code value="ORPHA:2405" />
        <display value="Thickened earlobes-conductive deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2406" />
        <display value="Locked-in syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2407" />
        <display value="LOC syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:240760" />
        <display value="Nijmegen breakage syndrome-like disorder" />
      </concept>
      <concept>
        <code value="ORPHA:2408" />
        <display value="Lowe-Kohn-Cohen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2409" />
        <display value="Lowry-MacLean syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:241" />
        <display value="Dyschromatosis universalis hereditaria" />
      </concept>
      <concept>
        <code value="ORPHA:2410" />
        <display value="Hypergonadotropic hypogonadism-cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2412" />
        <display value="Dislocation of the hip-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2414" />
        <display value="Congenital pulmonary lymphangiectasia" />
      </concept>
      <concept>
        <code value="ORPHA:2415" />
        <display value="Rare lymphatic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:242" />
        <display value="46,XY complete gonadal dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:2420" />
        <display value="Primary pulmonary lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:2427" />
        <display value="Macrocephaly-short stature-paraplegia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2429" />
        <display value="Macrocephaly-spastic paraplegia-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:243" />
        <display value="46,XX gonadal dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:2430" />
        <display value="Congenital macroglossia" />
      </concept>
      <concept>
        <code value="ORPHA:2431" />
        <display value="Central bilateral macrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:2432" />
        <display value="Macrosomia-microphthalmia-cleft palate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:243343" />
        <display value="Dimethylglycine dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:243367" />
        <display value="Acute fatty liver of pregnancy" />
      </concept>
      <concept>
        <code value="ORPHA:2435" />
        <display value="Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2437" />
        <display value="Czeizel-Losonci syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2438" />
        <display value="Hand-foot-genital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2439" />
        <display value="Patterson-Stevenson-Fontaine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:244" />
        <display value="Primary ciliary dyskinesia" />
      </concept>
      <concept>
        <code value="ORPHA:2440" />
        <display value="Isolated split hand-split foot malformation" />
      </concept>
      <concept>
        <code value="ORPHA:2442" />
        <display value="X-linked lymphoproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:244242" />
        <display value="HELLP syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:244283" />
        <display value="Biliary atresia with splenic malformation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2443" />
        <display value="Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:244305" />
        <display value="Dominant hypophosphatemia with nephrolithiasis or osteoporosis" />
      </concept>
      <concept>
        <code value="ORPHA:244310" />
        <display value="RFT1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:2444" />
        <display value="Congenital pulmonary airway malformation" />
      </concept>
      <concept>
        <code value="ORPHA:2445" />
        <display value="Conotruncal heart malformations" />
      </concept>
      <concept>
        <code value="ORPHA:2447" />
        <display value="Congenital mitral malformation" />
      </concept>
      <concept>
        <code value="ORPHA:245" />
        <display value="Nager syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2451" />
        <display value="Mucocutaneous venous malformations" />
      </concept>
      <concept>
        <code value="ORPHA:2456" />
        <display value="Familial supernumerary nipples" />
      </concept>
      <concept>
        <code value="ORPHA:2457" />
        <display value="Mandibuloacral dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2459" />
        <display value="Mansonelliasis" />
      </concept>
      <concept>
        <code value="ORPHA:246" />
        <display value="Postaxial acrofacial dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:2460" />
        <display value="Van den Ende-Gupta syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2461" />
        <display value="Marden-Walker syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2462" />
        <display value="Shprintzen-Goldberg syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2463" />
        <display value="Marfanoid habitus-autosomal recessive intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2464" />
        <display value="Marfanoid syndrome, De Silva type" />
      </concept>
      <concept>
        <code value="ORPHA:2466" />
        <display value="MASA syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2467" />
        <display value="Systemic mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:247" />
        <display value="Arrhythmogenic right ventricular cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2470" />
        <display value="Matthew-Wood syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2471" />
        <display value="McDonough syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:247165" />
        <display value="Infantile mercury poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:247198" />
        <display value="Progressive cerebello-cerebral atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:247203" />
        <display value="Collecting duct carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:247234" />
        <display value="Sporadic adult-onset ataxia of unknown etiology" />
      </concept>
      <concept>
        <code value="ORPHA:247239" />
        <display value="Non-hereditary degenerative ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:247242" />
        <display value="Acquired ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:247245" />
        <display value="Superficial siderosis" />
      </concept>
      <concept>
        <code value="ORPHA:247257" />
        <display value="Inhalational anthrax" />
      </concept>
      <concept>
        <code value="ORPHA:247262" />
        <display value="Hyperphosphatasia-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2473" />
        <display value="McKusick-Kaufman syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:247353" />
        <display value="Generalized pustular psoriasis" />
      </concept>
      <concept>
        <code value="ORPHA:247378" />
        <display value="Autosomal recessive secondary polycythemia not associated with VHL gene" />
      </concept>
      <concept>
        <code value="ORPHA:2475" />
        <display value="White forelock with malformations" />
      </concept>
      <concept>
        <code value="ORPHA:247511" />
        <display value="Autosomal dominant secondary polycythemia" />
      </concept>
      <concept>
        <code value="ORPHA:247522" />
        <display value="Primary ciliary dyskinesia-retinitis pigmentosa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:247525" />
        <display value="Citrullinemia type I" />
      </concept>
      <concept>
        <code value="ORPHA:247546" />
        <display value="Acute neonatal citrullinemia type I" />
      </concept>
      <concept>
        <code value="ORPHA:247573" />
        <display value="Adult-onset citrullinemia type I" />
      </concept>
      <concept>
        <code value="ORPHA:247582" />
        <display value="Citrin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:247585" />
        <display value="Citrullinemia type II" />
      </concept>
      <concept>
        <code value="ORPHA:247598" />
        <display value="Neonatal intrahepatic cholestasis due to citrin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2476" />
        <display value="Dysraphism-cleft lip/palate-limb reduction defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:247604" />
        <display value="Juvenile primary lateral sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:247623" />
        <display value="Perinatal lethal hypophosphatasia" />
      </concept>
      <concept>
        <code value="ORPHA:247638" />
        <display value="Prenatal benign hypophosphatasia" />
      </concept>
      <concept>
        <code value="ORPHA:247651" />
        <display value="Infantile hypophosphatasia" />
      </concept>
      <concept>
        <code value="ORPHA:247667" />
        <display value="Childhood-onset hypophosphatasia" />
      </concept>
      <concept>
        <code value="ORPHA:247676" />
        <display value="Adult hypophosphatasia" />
      </concept>
      <concept>
        <code value="ORPHA:247685" />
        <display value="Odontohypophosphatasia" />
      </concept>
      <concept>
        <code value="ORPHA:247691" />
        <display value="Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations" />
      </concept>
      <concept>
        <code value="ORPHA:247698" />
        <display value="Multiple endocrine neoplasia type 2A" />
      </concept>
      <concept>
        <code value="ORPHA:2477" />
        <display value="Megalencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:247709" />
        <display value="Multiple endocrine neoplasia type 2B" />
      </concept>
      <concept>
        <code value="ORPHA:247718" />
        <display value="Inflammatory myopathy with abundant macrophages" />
      </concept>
      <concept>
        <code value="ORPHA:247724" />
        <display value="Idiopathic eosinophilic myositis" />
      </concept>
      <concept>
        <code value="ORPHA:247762" />
        <display value="Lipoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:247765" />
        <display value="X-linked cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:247768" />
        <display value="Mullerian aplasia and hyperandrogenism" />
      </concept>
      <concept>
        <code value="ORPHA:247775" />
        <display value="Mayer-Rokitansky-Kuster-Hauser syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:247790" />
        <display value="FTH1-related iron overload" />
      </concept>
      <concept>
        <code value="ORPHA:247794" />
        <display value="Juvenile cataract-microcornea-renal glucosuria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:247798" />
        <display value="MUTYH-related attenuated familial adenomatous polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:2478" />
        <display value="Megalencephalic leukoencephalopathy with subcortical cysts" />
      </concept>
      <concept>
        <code value="ORPHA:247806" />
        <display value="APC-related attenuated familial adenomatous polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:247815" />
        <display value="Autosomal recessive ataxia due to PEX10 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:247820" />
        <display value="Ectodermal dysplasia-syndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:247827" />
        <display value="Ectodermal dysplasia-cutaneous syndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:247834" />
        <display value="Occult macular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:247839" />
        <display value="Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:247846" />
        <display value="Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:247854" />
        <display value="Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:247861" />
        <display value="Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:247868" />
        <display value="NLRP12-associated hereditary periodic fever syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2479" />
        <display value="Megalocornea-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:248" />
        <display value="Autosomal recessive hypohidrotic ectodermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:248095" />
        <display value="Primary hypertrophic osteoarthropathy" />
      </concept>
      <concept>
        <code value="ORPHA:2481" />
        <display value="Neurocutaneous melanocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:248111" />
        <display value="Juvenile Huntington disease" />
      </concept>
      <concept>
        <code value="ORPHA:2482" />
        <display value="Melhem-Fahl syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:248293" />
        <display value="Rare deficiency anemia" />
      </concept>
      <concept>
        <code value="ORPHA:248296" />
        <display value="Constitutional deficiency anemia" />
      </concept>
      <concept>
        <code value="ORPHA:2483" />
        <display value="Melkersson-Rosenthal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:248302" />
        <display value="Rare acquired deficiency anemia" />
      </concept>
      <concept>
        <code value="ORPHA:248308" />
        <display value="Rare hemorrhagic disorder" />
      </concept>
      <concept>
        <code value="ORPHA:248315" />
        <display value="Rare hemorrhagic disorder due to a coagulation factors defect" />
      </concept>
      <concept>
        <code value="ORPHA:248326" />
        <display value="Rare hemorrhagic disorder due to a platelet anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:248340" />
        <display value="Isolated delta-storage pool disease" />
      </concept>
      <concept>
        <code value="ORPHA:248347" />
        <display value="Rare hemorrhagic disorder due to an acquired platelet anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:248358" />
        <display value="Rare thrombotic disorder due to a coagulation factors defect" />
      </concept>
      <concept>
        <code value="ORPHA:248361" />
        <display value="Rare thrombotic disorder due to a constitutional coagulation factors defect" />
      </concept>
      <concept>
        <code value="ORPHA:248365" />
        <display value="Rare thrombotic disorder due to an acquired coagulation factors defect" />
      </concept>
      <concept>
        <code value="ORPHA:248368" />
        <display value="Rare thrombotic disorder due to a platelet anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:2484" />
        <display value="Melnick-Needles syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:248401" />
        <display value="Rare thrombotic disorder due to a constitutional platelet anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:248404" />
        <display value="Rare thrombotic disorder due to an acquired platelet anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:248408" />
        <display value="Familial hypodysfibrinogenemia" />
      </concept>
      <concept>
        <code value="ORPHA:2485" />
        <display value="Melorheostosis" />
      </concept>
      <concept>
        <code value="ORPHA:2487" />
        <display value="Lower limb malformation-hypospadias syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2489" />
        <display value="Upper limb defect-eye and ear abnormalities syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:249" />
        <display value="Fibrous dysplasia of bone" />
      </concept>
      <concept>
        <code value="ORPHA:2491" />
        <display value="Mullerian duct anomalies-limb anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2492" />
        <display value="FATCO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2494" />
        <display value="MenEtrier disease" />
      </concept>
      <concept>
        <code value="ORPHA:2495" />
        <display value="Meningioma" />
      </concept>
      <concept>
        <code value="ORPHA:2496" />
        <display value="Mesomelia-synostoses syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2497" />
        <display value="Upper limb mesomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2498" />
        <display value="Syndactyly type 8" />
      </concept>
      <concept>
        <code value="ORPHA:2499" />
        <display value="Metachondromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:25" />
        <display value="Glutaryl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:250" />
        <display value="Frontonasal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2500" />
        <display value="Acrogeria" />
      </concept>
      <concept>
        <code value="ORPHA:2501" />
        <display value="Metaphyseal chondrodysplasia, Spahr type" />
      </concept>
      <concept>
        <code value="ORPHA:250165" />
        <display value="Genetic polycythemia" />
      </concept>
      <concept>
        <code value="ORPHA:2502" />
        <display value="Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2504" />
        <display value="Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2505" />
        <display value="Multiple benign circumferential skin creases on limbs" />
      </concept>
      <concept>
        <code value="ORPHA:2508" />
        <display value="Corpus callosum agenesis-abnormal genitalia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:250831" />
        <display value="Logopenic progressive aphasia" />
      </concept>
      <concept>
        <code value="ORPHA:250908" />
        <display value="Rare neoplastic disease" />
      </concept>
      <concept>
        <code value="ORPHA:250923" />
        <display value="Isolated aniridia" />
      </concept>
      <concept>
        <code value="ORPHA:250932" />
        <display value="Autosomal dominant optic atrophy and peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:250972" />
        <display value="Polymicrogyria with optic nerve hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:250977" />
        <display value="AICA-ribosiduria" />
      </concept>
      <concept>
        <code value="ORPHA:250984" />
        <display value="Autosomal recessive Stickler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:250989" />
        <display value="1q21.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:250994" />
        <display value="1q21.1 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:250999" />
        <display value="1q41q42 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251" />
        <display value="Multiple epiphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2510" />
        <display value="Micro syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251004" />
        <display value="Paternal uniparental disomy of chromosome 1" />
      </concept>
      <concept>
        <code value="ORPHA:251009" />
        <display value="Maternal uniparental disomy of chromosome 1" />
      </concept>
      <concept>
        <code value="ORPHA:251014" />
        <display value="2q31.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251019" />
        <display value="2q32q33 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251028" />
        <display value="2q33.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251038" />
        <display value="3q29 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251043" />
        <display value="Ring chromosome 5 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251046" />
        <display value="6p22 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251056" />
        <display value="6q25 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251061" />
        <display value="7q31 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251066" />
        <display value="8p11.2 deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251071" />
        <display value="8p23.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251076" />
        <display value="8p23.1 duplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2511" />
        <display value="Microbrachycephaly-ptosis-cleft lip syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2512" />
        <display value="Autosomal recessive primary microcephaly" />
      </concept>
      <concept>
        <code value="ORPHA:251262" />
        <display value="Familial osteochondritis dissecans" />
      </concept>
      <concept>
        <code value="ORPHA:251274" />
        <display value="Familial hyperaldosteronism type III" />
      </concept>
      <concept>
        <code value="ORPHA:251279" />
        <display value="Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251282" />
        <display value="Autosomal dominant spastic ataxia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:251287" />
        <display value="Benign concentric annular macular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:251290" />
        <display value="Parietal foramina with clavicular hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:251295" />
        <display value="Pigmented paravenous retinochoroidal atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2513" />
        <display value="Microcephaly-albinism-digital anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251304" />
        <display value="Infantile onset panniculitis with uveitis and systemic granulomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:251307" />
        <display value="Idiopathic recurrent pericarditis" />
      </concept>
      <concept>
        <code value="ORPHA:251312" />
        <display value="Overlapping connective tissue disease" />
      </concept>
      <concept>
        <code value="ORPHA:251325" />
        <display value="Drug-induced vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:251328" />
        <display value="Unclassified vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:251332" />
        <display value="Unexplained long-lasting fever/inflammatory syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251347" />
        <display value="Ataxia-telangiectasia-like disorder" />
      </concept>
      <concept>
        <code value="ORPHA:251355" />
        <display value="Sickle cell disease associated with an other hemoglobin anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:251359" />
        <display value="Sickle cell-beta-thalassemia disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251365" />
        <display value="Sickle cell-hemoglobin C disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251370" />
        <display value="Sickle cell-hemoglobin D disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251375" />
        <display value="Sickle cell-hemoglobin E disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251380" />
        <display value="Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251383" />
        <display value="CK syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251393" />
        <display value="Localized junctional epidermolysis bullosa, non-Herlitz type" />
      </concept>
      <concept>
        <code value="ORPHA:2514" />
        <display value="Autosomal dominant primary microcephaly" />
      </concept>
      <concept>
        <code value="ORPHA:2515" />
        <display value="Microcephaly-cardiomyopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251510" />
        <display value="46,XY partial gonadal dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:251515" />
        <display value="Distal arthrogryposis type 10" />
      </concept>
      <concept>
        <code value="ORPHA:251523" />
        <display value="Hyperzincemia and hypercalprotectinemia" />
      </concept>
      <concept>
        <code value="ORPHA:251529" />
        <display value="Toxic or drug-related embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:251535" />
        <display value="Maternal disease-related embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:251558" />
        <display value="Rare tumor of neuroepithelial tissue" />
      </concept>
      <concept>
        <code value="ORPHA:251561" />
        <display value="High-grade astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251576" />
        <display value="Gliosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:251579" />
        <display value="Giant cell glioblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:251582" />
        <display value="Gliomatosis cerebri" />
      </concept>
      <concept>
        <code value="ORPHA:251589" />
        <display value="Anaplastic astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251592" />
        <display value="Low-grade astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251595" />
        <display value="Diffuse astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251598" />
        <display value="Protoplasmic astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:2516" />
        <display value="Microcephaly-cardiac defect-lung malsegmentation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251601" />
        <display value="Fibrillary astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251604" />
        <display value="Gemistocytic astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251607" />
        <display value="Pleomorphic xanthoastrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251612" />
        <display value="Pilocytic astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251615" />
        <display value="Pilomyxoid astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251618" />
        <display value="Subependymal giant cell astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251623" />
        <display value="Pituicytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251627" />
        <display value="Oligodendroglioma" />
      </concept>
      <concept>
        <code value="ORPHA:251630" />
        <display value="Anaplastic oligodendroglioma" />
      </concept>
      <concept>
        <code value="ORPHA:251633" />
        <display value="Low grade ependymoma" />
      </concept>
      <concept>
        <code value="ORPHA:251636" />
        <display value="Ependymoma" />
      </concept>
      <concept>
        <code value="ORPHA:251639" />
        <display value="Subependymoma" />
      </concept>
      <concept>
        <code value="ORPHA:251643" />
        <display value="Myxopapillary ependymoma" />
      </concept>
      <concept>
        <code value="ORPHA:251646" />
        <display value="Anaplastic ependymoma" />
      </concept>
      <concept>
        <code value="ORPHA:251651" />
        <display value="Oligoastrocytic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:251656" />
        <display value="Oligoastrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251663" />
        <display value="Anaplastic oligoastrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251668" />
        <display value="Glial tumor of neuroepithelial tissue with unknown origin" />
      </concept>
      <concept>
        <code value="ORPHA:251671" />
        <display value="Angiocentric glioma" />
      </concept>
      <concept>
        <code value="ORPHA:251674" />
        <display value="Chordoid glioma" />
      </concept>
      <concept>
        <code value="ORPHA:251679" />
        <display value="Astroblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:2518" />
        <display value="Autosomal recessive chorioretinopathy-microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251852" />
        <display value="Embryonal tumor of neuroepithelial tissue" />
      </concept>
      <concept>
        <code value="ORPHA:251855" />
        <display value="Anaplastic/large cell medulloblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:251858" />
        <display value="Medulloblastoma with extensive nodularity" />
      </concept>
      <concept>
        <code value="ORPHA:251863" />
        <display value="Desmoplastic/nodular medulloblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:251867" />
        <display value="Classic medulloblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:251870" />
        <display value="Central nervous system primitive neuroectodermal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:251877" />
        <display value="Ganglioneuroblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:251880" />
        <display value="Ependymoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:251883" />
        <display value="Medulloepithelioma of the central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:251896" />
        <display value="Choroid plexus tumor" />
      </concept>
      <concept>
        <code value="ORPHA:251899" />
        <display value="Choroid plexus carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:2519" />
        <display value="Microcephaly-seizures-intellectual disability-heart disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:251902" />
        <display value="Atypical papilloma of choroid plexus" />
      </concept>
      <concept>
        <code value="ORPHA:251905" />
        <display value="Pineal tumor of neuroepithelial tissue" />
      </concept>
      <concept>
        <code value="ORPHA:251909" />
        <display value="Pineoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:251912" />
        <display value="Pineocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251915" />
        <display value="Papillary tumor of the pineal region" />
      </concept>
      <concept>
        <code value="ORPHA:251919" />
        <display value="Pineal parenchymal tumor of intermediate differenciation" />
      </concept>
      <concept>
        <code value="ORPHA:251924" />
        <display value="Neuronal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:251927" />
        <display value="Extraventricular neurocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251931" />
        <display value="Cerebellar liponeurocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251934" />
        <display value="Mixed neuronal-glial tumor" />
      </concept>
      <concept>
        <code value="ORPHA:251937" />
        <display value="Gangliocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:251940" />
        <display value="Desmoplastic infantile astrocytoma/ganglioglioma" />
      </concept>
      <concept>
        <code value="ORPHA:251946" />
        <display value="Dysembryoplastic neuroepithelial tumor" />
      </concept>
      <concept>
        <code value="ORPHA:251949" />
        <display value="Ganglioglioma" />
      </concept>
      <concept>
        <code value="ORPHA:251957" />
        <display value="Anaplastic ganglioglioma" />
      </concept>
      <concept>
        <code value="ORPHA:251962" />
        <display value="Papillary glioneuronal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:251975" />
        <display value="Rosette-forming glioneuronal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:251992" />
        <display value="Ganglioneuroma" />
      </concept>
      <concept>
        <code value="ORPHA:251995" />
        <display value="Primary germ cell tumor of central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:252006" />
        <display value="Yolk sac tumor of central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:252015" />
        <display value="Choriocarcinoma of the central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:252018" />
        <display value="Teratoma of the central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:252021" />
        <display value="Mixed germ cell tumor of central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:252025" />
        <display value="Tumor of meninges" />
      </concept>
      <concept>
        <code value="ORPHA:252028" />
        <display value="Primary melanocytic tumor of central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:252031" />
        <display value="Diffuse leptomeningeal melanocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:252046" />
        <display value="Meningeal melanocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:252050" />
        <display value="Primary melanoma of the central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:252054" />
        <display value="Hemangioblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:252057" />
        <display value="Tumor of cranial and spinal nerves" />
      </concept>
      <concept>
        <code value="ORPHA:2521" />
        <display value="Microcephaly-cleft palate-abnormal retinal pigmentation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:252128" />
        <display value="Malignant peripheral nerve sheath tumor with perineurial differentiation" />
      </concept>
      <concept>
        <code value="ORPHA:252131" />
        <display value="Benign peripheral nerve sheath tumor" />
      </concept>
      <concept>
        <code value="ORPHA:252164" />
        <display value="Benign schwannoma" />
      </concept>
      <concept>
        <code value="ORPHA:252175" />
        <display value="Vestibular schwannoma" />
      </concept>
      <concept>
        <code value="ORPHA:252183" />
        <display value="Neurofibroma" />
      </concept>
      <concept>
        <code value="ORPHA:252190" />
        <display value="Inherited nervous system cancer-predisposing syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2522" />
        <display value="Microcephaly-cervical spine fusion anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:252202" />
        <display value="Constitutional mismatch repair deficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:252206" />
        <display value="Melanoma and neural system tumor syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:252212" />
        <display value="Malignant triton tumor" />
      </concept>
      <concept>
        <code value="ORPHA:2523" />
        <display value="Microcephaly-brain defect-spasticity-hypernatremia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2524" />
        <display value="Pontocerebellar hypoplasia type 2" />
      </concept>
      <concept>
        <code value="ORPHA:2526" />
        <display value="Microcephaly-lymphedema-chorioretinopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2528" />
        <display value="Microcephaly-microcornea syndrome, Seemanova type" />
      </concept>
      <concept>
        <code value="ORPHA:253" />
        <display value="Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2533" />
        <display value="Microcephaly-deafness-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2535" />
        <display value="Microcornea-corectopia-macular hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2536" />
        <display value="Microcornea-glaucoma-absent frontal sinuses syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2538" />
        <display value="Microgastria-limb reduction defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254" />
        <display value="Spondylometaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2542" />
        <display value="Isolated microphthalmia-anophthalmia-coloboma" />
      </concept>
      <concept>
        <code value="ORPHA:254334" />
        <display value="Autosomal recessive intermediate Charcot-Marie-Tooth disease type B" />
      </concept>
      <concept>
        <code value="ORPHA:254343" />
        <display value="Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254346" />
        <display value="19p13.12 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254351" />
        <display value="Distal 7q11.23 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254361" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2Q" />
      </concept>
      <concept>
        <code value="ORPHA:254367" />
        <display value="Rare lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:254370" />
        <display value="Rare cutaneous lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:254373" />
        <display value="Rare mucosal lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:254379" />
        <display value="Linear lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:254395" />
        <display value="Actinic lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:254411" />
        <display value="Annular atrophic lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:254424" />
        <display value="Annular lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:254449" />
        <display value="Atrophic lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:254463" />
        <display value="Lichen planus pigmentosus" />
      </concept>
      <concept>
        <code value="ORPHA:254478" />
        <display value="Lichen planus pemphigoides" />
      </concept>
      <concept>
        <code value="ORPHA:254492" />
        <display value="Frontal fibrosing alopecia" />
      </concept>
      <concept>
        <code value="ORPHA:254504" />
        <display value="Inhalational botulism" />
      </concept>
      <concept>
        <code value="ORPHA:254509" />
        <display value="Iatrogenic botulism" />
      </concept>
      <concept>
        <code value="ORPHA:254516" />
        <display value="Temple syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254519" />
        <display value="Kagami-Ogata syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254525" />
        <display value="Temple syndrome due to paternal 14q32.2 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:254528" />
        <display value="Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:254531" />
        <display value="Temple syndrome due to paternal 14q32.2 hypomethylation" />
      </concept>
      <concept>
        <code value="ORPHA:254534" />
        <display value="Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation" />
      </concept>
      <concept>
        <code value="ORPHA:254685" />
        <display value="Gestational trophoblastic disease" />
      </concept>
      <concept>
        <code value="ORPHA:254688" />
        <display value="Complete hydatidiform mole" />
      </concept>
      <concept>
        <code value="ORPHA:254693" />
        <display value="Partial hydatidiform mole" />
      </concept>
      <concept>
        <code value="ORPHA:254698" />
        <display value="Epithelioid trophoblastic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:2547" />
        <display value="Microphthalmia-microtia-fetal akinesia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254704" />
        <display value="Genetic hyperferritinemia without iron overload" />
      </concept>
      <concept>
        <code value="ORPHA:254746" />
        <display value="Pyruvate metabolism disorder" />
      </concept>
      <concept>
        <code value="ORPHA:254749" />
        <display value="Tricarboxylic acid cycle disorder" />
      </concept>
      <concept>
        <code value="ORPHA:254758" />
        <display value="Mitochondrial oxidative phosphorylation disorder due to mitochondrial DNA anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:254767" />
        <display value="Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA" />
      </concept>
      <concept>
        <code value="ORPHA:254776" />
        <display value="Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA" />
      </concept>
      <concept>
        <code value="ORPHA:254788" />
        <display value="Mitochondrial DNA-related mitochondrial myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:254793" />
        <display value="Mitochondrial oxidative phosphorylation disorder due to a duplication of mitochondrial DNA" />
      </concept>
      <concept>
        <code value="ORPHA:254803" />
        <display value="Mitochondrial DNA depletion syndrome, encephalomyopathic form" />
      </concept>
      <concept>
        <code value="ORPHA:254807" />
        <display value="Multiple mitochondrial DNA deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254818" />
        <display value="Ataxia neuropathy spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:254822" />
        <display value="Mitochondrial oxidative phosphorylation disorder with no known mechanism" />
      </concept>
      <concept>
        <code value="ORPHA:254827" />
        <display value="Mitochondrial membrane transport disorder" />
      </concept>
      <concept>
        <code value="ORPHA:254830" />
        <display value="Mitochondrial substrate carrier disorder" />
      </concept>
      <concept>
        <code value="ORPHA:254834" />
        <display value="Mitochondrial protein import disorder" />
      </concept>
      <concept>
        <code value="ORPHA:254837" />
        <display value="Unspecified mitochondrial disorder" />
      </concept>
      <concept>
        <code value="ORPHA:254843" />
        <display value="Exercise intolerance with lactic acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:254846" />
        <display value="Isolated oxidative phosphorylation complex disorder" />
      </concept>
      <concept>
        <code value="ORPHA:254851" />
        <display value="Mitochondrial DNA-related dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:254854" />
        <display value="Pure mitochondrial myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:254857" />
        <display value="Lethal infantile mitochondrial myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:254864" />
        <display value="Mitochondrial myopathy with reversible cytochrome C oxidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:254871" />
        <display value="Mitochondrial DNA depletion syndrome, hepatocerebral form" />
      </concept>
      <concept>
        <code value="ORPHA:254875" />
        <display value="Mitochondrial DNA depletion syndrome, myopathic form" />
      </concept>
      <concept>
        <code value="ORPHA:254881" />
        <display value="Spinocerebellar ataxia with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:254886" />
        <display value="Autosomal recessive progressive external ophthalmoplegia" />
      </concept>
      <concept>
        <code value="ORPHA:254892" />
        <display value="Autosomal dominant progressive external ophthalmoplegia" />
      </concept>
      <concept>
        <code value="ORPHA:254898" />
        <display value="Deafness-encephaloneuropathy-obesity-valvulopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2549" />
        <display value="Oculoauriculovertebral spectrum with radial defects" />
      </concept>
      <concept>
        <code value="ORPHA:254902" />
        <display value="Renal tubulopathy-encephalopathy-liver failure syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:254905" />
        <display value="Isolated cytochrome C oxidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:254913" />
        <display value="Isolated ATP synthase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:254920" />
        <display value="Combined oxidative phosphorylation defect type 2" />
      </concept>
      <concept>
        <code value="ORPHA:254925" />
        <display value="Combined oxidative phosphorylation defect type 4" />
      </concept>
      <concept>
        <code value="ORPHA:254930" />
        <display value="Combined oxidative phosphorylation defect type 7" />
      </concept>
      <concept>
        <code value="ORPHA:255" />
        <display value="Dopa-responsive dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:2551" />
        <display value="Microspherophakia-metaphyseal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:255132" />
        <display value="Adult-onset autosomal recessive sideroblastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:255138" />
        <display value="Pyruvate dehydrogenase E1-beta deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:255182" />
        <display value="Pyruvate dehydrogenase E3-binding protein deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2552" />
        <display value="Microsporidiosis" />
      </concept>
      <concept>
        <code value="ORPHA:255210" />
        <display value="Mitochondrial DNA-associated Leigh syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:255229" />
        <display value="Navajo neurohepatopathy" />
      </concept>
      <concept>
        <code value="ORPHA:255235" />
        <display value="Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:255241" />
        <display value="Leigh syndrome with leukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:255249" />
        <display value="Leigh syndrome with nephrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2554" />
        <display value="Ear-patella-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2556" />
        <display value="Microphthalmia with linear skin defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2557" />
        <display value="Mietens syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2558" />
        <display value="Mikati-Najjar-Sahli syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:256" />
        <display value="Early-onset generalized limb-onset dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:2560" />
        <display value="Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2561" />
        <display value="Pyramidal molars-abnormal upper lip syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2563" />
        <display value="MOMO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2564" />
        <display value="Tetramelic monodactyly" />
      </concept>
      <concept>
        <code value="ORPHA:2565" />
        <display value="Mononen-Karnes-Senac syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2566" />
        <display value="Chronic Epstein-Barr virus infection syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:257" />
        <display value="Epidermolysis bullosa simplex with muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2570" />
        <display value="Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2571" />
        <display value="X-linked immunoneurologic disorder" />
      </concept>
      <concept>
        <code value="ORPHA:2572" />
        <display value="Spastic ataxia-corneal dystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2573" />
        <display value="Moyamoya disease" />
      </concept>
      <concept>
        <code value="ORPHA:2574" />
        <display value="Moynahan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2575" />
        <display value="Cystic fibrosis-gastritis-megaloblastic anemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2576" />
        <display value="MULIBREY nanism" />
      </concept>
      <concept>
        <code value="ORPHA:2578" />
        <display value="Mayer-Rokitansky-Kuster-Hauser syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:2579" />
        <display value="Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:258" />
        <display value="Congenital muscular dystrophy type 1A" />
      </concept>
      <concept>
        <code value="ORPHA:2580" />
        <display value="Shoulder and girdle defects-familial intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2582" />
        <display value="Myalgia-eosinophilia syndrome associated with tryptophan" />
      </concept>
      <concept>
        <code value="ORPHA:2583" />
        <display value="Mycetoma" />
      </concept>
      <concept>
        <code value="ORPHA:2584" />
        <display value="Classic mycosis fungoides" />
      </concept>
      <concept>
        <code value="ORPHA:2585" />
        <display value="Ataxia-pancytopenia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2587" />
        <display value="Myeloperoxidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2588" />
        <display value="Myhre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2589" />
        <display value="Myoclonus-cerebellar ataxia-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2590" />
        <display value="Spinal muscular atrophy-progressive myoclonic epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2591" />
        <display value="Infantile myofibromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:2593" />
        <display value="Tubular aggregate myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2596" />
        <display value="Myopathy and diabetes mellitus" />
      </concept>
      <concept>
        <code value="ORPHA:25968" />
        <display value="Benign occipital epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:2597" />
        <display value="Mitochondrial myopathy-lactic acidosis-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2598" />
        <display value="Mitochondrial myopathy and sideroblastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:25980" />
        <display value="X-linked myopathy with excessive autophagy" />
      </concept>
      <concept>
        <code value="ORPHA:26" />
        <display value="Methylmalonic acidemia with homocystinuria" />
      </concept>
      <concept>
        <code value="ORPHA:2601" />
        <display value="Myopathy-growth delay-intellectual disability-hypospadias syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:260305" />
        <display value="Autosomal recessive sideroblastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:2604" />
        <display value="Familial visceral myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2608" />
        <display value="N syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2609" />
        <display value="Isolated complex I deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:261" />
        <display value="Emery-Dreifuss muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:26106" />
        <display value="Hereditary diffuse gastric cancer" />
      </concept>
      <concept>
        <code value="ORPHA:2611" />
        <display value="Linear verrucous nevus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261102" />
        <display value="Distal 7q11.23 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261112" />
        <display value="Monosomy 9p" />
      </concept>
      <concept>
        <code value="ORPHA:261120" />
        <display value="14q11.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261144" />
        <display value="14q12 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261183" />
        <display value="15q11.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261190" />
        <display value="15q14 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261197" />
        <display value="Proximal 16p11.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2612" />
        <display value="Linear nevus sebaceus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261204" />
        <display value="16p11.2p12.2 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261211" />
        <display value="16p11.2p12.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261222" />
        <display value="Distal 16p11.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261229" />
        <display value="14q11.2 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261236" />
        <display value="16p13.11 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261243" />
        <display value="16p13.11 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261250" />
        <display value="16q24.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261257" />
        <display value="Distal 17p13.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261265" />
        <display value="17q12 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261272" />
        <display value="17q12 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261279" />
        <display value="17q23.1q23.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261290" />
        <display value="Trisomy 17p" />
      </concept>
      <concept>
        <code value="ORPHA:261295" />
        <display value="20p12.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2613" />
        <display value="Nail-patella-like renal disease" />
      </concept>
      <concept>
        <code value="ORPHA:261304" />
        <display value="Paternal 20q13.2q13.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261311" />
        <display value="20q13.33 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261318" />
        <display value="Trisomy 20p" />
      </concept>
      <concept>
        <code value="ORPHA:261323" />
        <display value="21q22.11q22.12 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261330" />
        <display value="Distal 22q11.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261337" />
        <display value="Distal 22q11.2 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261344" />
        <display value="Trisomy 1q" />
      </concept>
      <concept>
        <code value="ORPHA:261349" />
        <display value="2p15p16.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:26137" />
        <display value="Juvenile temporal arteritis" />
      </concept>
      <concept>
        <code value="ORPHA:2614" />
        <display value="Nail-patella syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261476" />
        <display value="Xp21 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261483" />
        <display value="Xq27.3q28 duplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261494" />
        <display value="Kleefstra syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2615" />
        <display value="Nakajo-Nishimura syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261501" />
        <display value="Atypical Norrie disease due to monosomy Xp11.3" />
      </concept>
      <concept>
        <code value="ORPHA:261519" />
        <display value="Maternal uniparental disomy of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:261524" />
        <display value="Paternal uniparental disomy of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:261529" />
        <display value="Ring chromosome Y syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261534" />
        <display value="49,XXXYY syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261537" />
        <display value="Mowat-Wilson syndrome due to monosomy 2q22" />
      </concept>
      <concept>
        <code value="ORPHA:261552" />
        <display value="Mowat-Wilson syndrome due to a ZEB2 point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:261559" />
        <display value="Blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261572" />
        <display value="Blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261579" />
        <display value="Blepharophimosis-epicanthus inversus-ptosis due to copy number variations" />
      </concept>
      <concept>
        <code value="ORPHA:261584" />
        <display value="Familial adenomatous polyposis due to 5q22.2 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:2616" />
        <display value="3M syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:261600" />
        <display value="Alagille syndrome due to 20p12 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:261619" />
        <display value="Alagille syndrome due to a JAG1 point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:261629" />
        <display value="Alagille syndrome due to a NOTCH2 point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:261638" />
        <display value="Okihiro syndrome due to 20q13 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:261647" />
        <display value="Okihiro syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:261652" />
        <display value="Kleefstra syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:2617" />
        <display value="Microcephalic primordial dwarfism, Montreal type" />
      </concept>
      <concept>
        <code value="ORPHA:261766" />
        <display value="Partial deletion of chromosome 1" />
      </concept>
      <concept>
        <code value="ORPHA:261771" />
        <display value="Partial deletion of chromosome 2" />
      </concept>
      <concept>
        <code value="ORPHA:261776" />
        <display value="Partial deletion of chromosome 3" />
      </concept>
      <concept>
        <code value="ORPHA:261781" />
        <display value="Partial deletion of chromosome 4" />
      </concept>
      <concept>
        <code value="ORPHA:261786" />
        <display value="Partial deletion of chromosome 5" />
      </concept>
      <concept>
        <code value="ORPHA:261791" />
        <display value="Partial deletion of chromosome 6" />
      </concept>
      <concept>
        <code value="ORPHA:261796" />
        <display value="Partial deletion of chromosome 7" />
      </concept>
      <concept>
        <code value="ORPHA:261801" />
        <display value="Partial deletion of chromosome 8" />
      </concept>
      <concept>
        <code value="ORPHA:261806" />
        <display value="Partial deletion of chromosome 9" />
      </concept>
      <concept>
        <code value="ORPHA:261811" />
        <display value="Partial deletion of chromosome 10" />
      </concept>
      <concept>
        <code value="ORPHA:261816" />
        <display value="Partial deletion of chromosome 11" />
      </concept>
      <concept>
        <code value="ORPHA:261821" />
        <display value="Partial deletion of the long arm of chromosome 12" />
      </concept>
      <concept>
        <code value="ORPHA:261826" />
        <display value="Partial deletion of chromosome 16" />
      </concept>
      <concept>
        <code value="ORPHA:261831" />
        <display value="Partial deletion of chromosome 17" />
      </concept>
      <concept>
        <code value="ORPHA:261836" />
        <display value="Partial deletion of chromosome 18" />
      </concept>
      <concept>
        <code value="ORPHA:261841" />
        <display value="Partial deletion of chromosome 19" />
      </concept>
      <concept>
        <code value="ORPHA:261846" />
        <display value="Partial deletion of chromosome 20" />
      </concept>
      <concept>
        <code value="ORPHA:261857" />
        <display value="Partial deletion of the short arm of chromosome 1" />
      </concept>
      <concept>
        <code value="ORPHA:261866" />
        <display value="Partial deletion of the short arm of chromosome 2" />
      </concept>
      <concept>
        <code value="ORPHA:261875" />
        <display value="Partial deletion of the short arm of chromosome 3" />
      </concept>
      <concept>
        <code value="ORPHA:261884" />
        <display value="Partial deletion of the short arm of chromosome 4" />
      </concept>
      <concept>
        <code value="ORPHA:261893" />
        <display value="Partial deletion of the short arm of chromosome 5" />
      </concept>
      <concept>
        <code value="ORPHA:2619" />
        <display value="Brachydactylous dwarfism, Mseleni type" />
      </concept>
      <concept>
        <code value="ORPHA:261902" />
        <display value="Partial deletion of the short arm of chromosome 6" />
      </concept>
      <concept>
        <code value="ORPHA:261911" />
        <display value="Partial deletion of the short arm of chromosome 7" />
      </concept>
      <concept>
        <code value="ORPHA:261920" />
        <display value="Partial deletion of the short arm of chromosome 8" />
      </concept>
      <concept>
        <code value="ORPHA:261929" />
        <display value="Partial deletion of the short arm of chromosome 9" />
      </concept>
      <concept>
        <code value="ORPHA:261938" />
        <display value="Partial deletion of the short arm of chromosome 10" />
      </concept>
      <concept>
        <code value="ORPHA:261947" />
        <display value="Partial deletion of the short arm of chromosome 11" />
      </concept>
      <concept>
        <code value="ORPHA:261956" />
        <display value="Partial deletion of the short arm of chromosome 16" />
      </concept>
      <concept>
        <code value="ORPHA:261965" />
        <display value="Partial monosomy of the short arm of chromosome 17" />
      </concept>
      <concept>
        <code value="ORPHA:261974" />
        <display value="Partial deletion of the short arm of chromosome 18" />
      </concept>
      <concept>
        <code value="ORPHA:261983" />
        <display value="Partial deletion of the short arm of chromosome 19" />
      </concept>
      <concept>
        <code value="ORPHA:261992" />
        <display value="Partial monosomy of the short arm of chromosome 20" />
      </concept>
      <concept>
        <code value="ORPHA:262" />
        <display value="Duchenne and Becker muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:262001" />
        <display value="Partial deletion of the long arm of chromosome 1" />
      </concept>
      <concept>
        <code value="ORPHA:262010" />
        <display value="Partial deletion of the long arm of chromosome 2" />
      </concept>
      <concept>
        <code value="ORPHA:262019" />
        <display value="Partial deletion of the long arm of chromosome 3" />
      </concept>
      <concept>
        <code value="ORPHA:262029" />
        <display value="Partial deletion of the long arm of chromosome 4" />
      </concept>
      <concept>
        <code value="ORPHA:262038" />
        <display value="Partial deletion of the long arm of chromosome 5" />
      </concept>
      <concept>
        <code value="ORPHA:262047" />
        <display value="Partial deletion of the long arm of chromosome 6" />
      </concept>
      <concept>
        <code value="ORPHA:262056" />
        <display value="Partial deletion of the long arm of chromosome 7" />
      </concept>
      <concept>
        <code value="ORPHA:262065" />
        <display value="Partial deletion of the long arm of chromosome 8" />
      </concept>
      <concept>
        <code value="ORPHA:262074" />
        <display value="Partial monosomy of the long arm of chromosome 9" />
      </concept>
      <concept>
        <code value="ORPHA:262083" />
        <display value="Partial monosomy of the long arm of chromosome 10" />
      </concept>
      <concept>
        <code value="ORPHA:262092" />
        <display value="Partial deletion of the long arm of chromosome 11" />
      </concept>
      <concept>
        <code value="ORPHA:262101" />
        <display value="Partial deletion of the long arm of chromosome 13" />
      </concept>
      <concept>
        <code value="ORPHA:262110" />
        <display value="Partial deletion of the long arm of chromosome 14" />
      </concept>
      <concept>
        <code value="ORPHA:262119" />
        <display value="Partial deletion of the long arm of chromosome 15" />
      </concept>
      <concept>
        <code value="ORPHA:262128" />
        <display value="Partial deletion of the long arm of chromosome 16" />
      </concept>
      <concept>
        <code value="ORPHA:262137" />
        <display value="Partial deletion of the long arm of chromosome 17" />
      </concept>
      <concept>
        <code value="ORPHA:262146" />
        <display value="Partial deletion of the long arm of chromosome 18" />
      </concept>
      <concept>
        <code value="ORPHA:262155" />
        <display value="Partial deletion of the long arm of chromosome 19" />
      </concept>
      <concept>
        <code value="ORPHA:262164" />
        <display value="Partial deletion of the long arm of chromosome 20" />
      </concept>
      <concept>
        <code value="ORPHA:262173" />
        <display value="Partial deletion of the long arm of chromosome 21" />
      </concept>
      <concept>
        <code value="ORPHA:262182" />
        <display value="Partial deletion of the long arm of chromosome 22" />
      </concept>
      <concept>
        <code value="ORPHA:262191" />
        <display value="Partial duplication of chromosome 1" />
      </concept>
      <concept>
        <code value="ORPHA:262196" />
        <display value="Partial duplication of chromosome 2" />
      </concept>
      <concept>
        <code value="ORPHA:262201" />
        <display value="Partial duplication of chromosome 3" />
      </concept>
      <concept>
        <code value="ORPHA:262206" />
        <display value="Partial duplication of chromosome 4" />
      </concept>
      <concept>
        <code value="ORPHA:262211" />
        <display value="Partial trisomy/tetrasomy of chromosome 5" />
      </concept>
      <concept>
        <code value="ORPHA:2623" />
        <display value="Geleophysic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:262628" />
        <display value="Partial duplication of chromosome 6" />
      </concept>
      <concept>
        <code value="ORPHA:262633" />
        <display value="Partial duplication of chromosome 7" />
      </concept>
      <concept>
        <code value="ORPHA:262638" />
        <display value="Partial duplication of chromosome 8" />
      </concept>
      <concept>
        <code value="ORPHA:262643" />
        <display value="Partial trisomy/tetrasomy of chromosome 9" />
      </concept>
      <concept>
        <code value="ORPHA:262648" />
        <display value="Partial duplication of chromosome 10" />
      </concept>
      <concept>
        <code value="ORPHA:262653" />
        <display value="Partial duplication of chromosome 11" />
      </concept>
      <concept>
        <code value="ORPHA:262658" />
        <display value="Partial trisomy/tetrasomy of the short arm of chromosome 12" />
      </concept>
      <concept>
        <code value="ORPHA:262672" />
        <display value="Partial duplication of chromosome 16" />
      </concept>
      <concept>
        <code value="ORPHA:262677" />
        <display value="Partial duplication of chromosome 17" />
      </concept>
      <concept>
        <code value="ORPHA:262682" />
        <display value="Partial trisomy/tetrasomy of chromosome 18" />
      </concept>
      <concept>
        <code value="ORPHA:262687" />
        <display value="Partial duplication of chromosome 19" />
      </concept>
      <concept>
        <code value="ORPHA:262692" />
        <display value="Partial trisomy of chromosome 20" />
      </concept>
      <concept>
        <code value="ORPHA:262698" />
        <display value="Partial duplication of the short arm of chromosome 2" />
      </concept>
      <concept>
        <code value="ORPHA:262707" />
        <display value="Partial duplication of the short arm of chromosome 3" />
      </concept>
      <concept>
        <code value="ORPHA:262716" />
        <display value="Partial duplication of the short arm of chromosome 4" />
      </concept>
      <concept>
        <code value="ORPHA:262725" />
        <display value="Partial trisomy/tetrasomy of the short arm of chromosome 5" />
      </concept>
      <concept>
        <code value="ORPHA:262740" />
        <display value="Partial duplication of the short arm of chromosome 6" />
      </concept>
      <concept>
        <code value="ORPHA:262749" />
        <display value="Partial duplication of the short arm of chromosome 7" />
      </concept>
      <concept>
        <code value="ORPHA:262758" />
        <display value="Partial duplication of the short arm of chromosome 8" />
      </concept>
      <concept>
        <code value="ORPHA:262767" />
        <display value="Partial trisomy of the short arm of chromosome 9" />
      </concept>
      <concept>
        <code value="ORPHA:262776" />
        <display value="Partial duplication of the short arm of chromosome 10" />
      </concept>
      <concept>
        <code value="ORPHA:262785" />
        <display value="Partial duplication of the short arm of chromosome 11" />
      </concept>
      <concept>
        <code value="ORPHA:262794" />
        <display value="Partial duplication of the short arm of chromosome 16" />
      </concept>
      <concept>
        <code value="ORPHA:262803" />
        <display value="Partial duplication of the short arm of chromosome 17" />
      </concept>
      <concept>
        <code value="ORPHA:262812" />
        <display value="Partial trisomy/tetrasomy of the short arm of chromosome 18" />
      </concept>
      <concept>
        <code value="ORPHA:262833" />
        <display value="Partial duplication of the long arm of chromosome 1" />
      </concept>
      <concept>
        <code value="ORPHA:262842" />
        <display value="Partial duplication of the long arm of chromosome 2" />
      </concept>
      <concept>
        <code value="ORPHA:262851" />
        <display value="Partial duplication of the long arm of chromosome 3" />
      </concept>
      <concept>
        <code value="ORPHA:262860" />
        <display value="Partial duplication of the long arm of chromosome 4" />
      </concept>
      <concept>
        <code value="ORPHA:262869" />
        <display value="Partial trisomy of the long arm of chromosome 5" />
      </concept>
      <concept>
        <code value="ORPHA:262878" />
        <display value="Partial duplication of the long arm of chromosome 6" />
      </concept>
      <concept>
        <code value="ORPHA:262887" />
        <display value="Partial duplication of the long arm of chromosome 7" />
      </concept>
      <concept>
        <code value="ORPHA:262896" />
        <display value="Partial duplication of the long arm of chromosome 8" />
      </concept>
      <concept>
        <code value="ORPHA:262905" />
        <display value="Partial trisomy of the long arm of chromosome 9" />
      </concept>
      <concept>
        <code value="ORPHA:262914" />
        <display value="Partial duplication of the long arm of chromosome 10" />
      </concept>
      <concept>
        <code value="ORPHA:262923" />
        <display value="Partial duplication of the long arm of chromosome 11" />
      </concept>
      <concept>
        <code value="ORPHA:262932" />
        <display value="Partial duplication of the long arm of chromosome 13" />
      </concept>
      <concept>
        <code value="ORPHA:262941" />
        <display value="Partial duplication of the long arm of chromosome 14" />
      </concept>
      <concept>
        <code value="ORPHA:262950" />
        <display value="Partial duplication of the long arm of chromosome 15" />
      </concept>
      <concept>
        <code value="ORPHA:262959" />
        <display value="Partial trisomy of the long arm of chromosome 16" />
      </concept>
      <concept>
        <code value="ORPHA:262968" />
        <display value="Partial duplication of the long arm of chromosome 17" />
      </concept>
      <concept>
        <code value="ORPHA:262977" />
        <display value="Partial trisomy of the long arm of chromosome 18" />
      </concept>
      <concept>
        <code value="ORPHA:262986" />
        <display value="Partial duplication of the long arm of chromosome 19" />
      </concept>
      <concept>
        <code value="ORPHA:262995" />
        <display value="Partial trisomy of the long arm of chromosome 20" />
      </concept>
      <concept>
        <code value="ORPHA:263" />
        <display value="Limb-girdle muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:263004" />
        <display value="Partial duplication of the long arm of chromosome 22" />
      </concept>
      <concept>
        <code value="ORPHA:2631" />
        <display value="Mesomelic dwarfism-cleft palate-camptodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2632" />
        <display value="Langer mesomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:263297" />
        <display value="Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2633" />
        <display value="Mesomelic dysplasia, Nievergelt type" />
      </concept>
      <concept>
        <code value="ORPHA:263310" />
        <display value="Thymoma type A" />
      </concept>
      <concept>
        <code value="ORPHA:263317" />
        <display value="Thymoma type B" />
      </concept>
      <concept>
        <code value="ORPHA:263324" />
        <display value="Thymoma type AB" />
      </concept>
      <concept>
        <code value="ORPHA:263331" />
        <display value="Well-differentiated thymic neuroendocrine carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:263335" />
        <display value="Moderately-differentiated thymic neuroendocrine carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:263339" />
        <display value="Poorly differentiated thymic neuroendocrine carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:263347" />
        <display value="MRCS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:263355" />
        <display value="ATR-X-related syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2634" />
        <display value="Mesomelic dwarfism, Reinhardt-Pfeiffer type" />
      </concept>
      <concept>
        <code value="ORPHA:263410" />
        <display value="Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:263413" />
        <display value="Angiosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:263417" />
        <display value="Bartter syndrome with hypocalcemia" />
      </concept>
      <concept>
        <code value="ORPHA:263425" />
        <display value="Nevus of Ota" />
      </concept>
      <concept>
        <code value="ORPHA:263432" />
        <display value="Nevus of Ito" />
      </concept>
      <concept>
        <code value="ORPHA:263435" />
        <display value="Congenital smooth muscle hamartoma" />
      </concept>
      <concept>
        <code value="ORPHA:263440" />
        <display value="Neuroacanthocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:263455" />
        <display value="Hyperinsulinism due to HNF4A deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:263458" />
        <display value="Hyperinsulinism due to INSR deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:263463" />
        <display value="CHST3-related skeletal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:263479" />
        <display value="Fuchs heterochromic iridocyclitis" />
      </concept>
      <concept>
        <code value="ORPHA:26348" />
        <display value="Acquired prothrombin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:263482" />
        <display value="Spondyloepiphyseal dysplasia, Maroteaux type" />
      </concept>
      <concept>
        <code value="ORPHA:263487" />
        <display value="COG5-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:26349" />
        <display value="Protein S acquired deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:263494" />
        <display value="DPM3-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:2635" />
        <display value="Metatropic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:263501" />
        <display value="COG4-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:263508" />
        <display value="COG1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:263516" />
        <display value="Progressive myoclonic epilepsy type 3" />
      </concept>
      <concept>
        <code value="ORPHA:263524" />
        <display value="Acute necrotizing encephalopathy of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:263534" />
        <display value="Acral peeling skin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:263543" />
        <display value="Generalized peeling skin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:263548" />
        <display value="Peeling skin syndrome type A" />
      </concept>
      <concept>
        <code value="ORPHA:263553" />
        <display value="Peeling skin syndrome type B" />
      </concept>
      <concept>
        <code value="ORPHA:263558" />
        <display value="Peeling skin syndrome type C" />
      </concept>
      <concept>
        <code value="ORPHA:2636" />
        <display value="Microcephalic osteodysplastic primordial dwarfism types I and III" />
      </concept>
      <concept>
        <code value="ORPHA:263662" />
        <display value="Familial multiple meningioma" />
      </concept>
      <concept>
        <code value="ORPHA:263665" />
        <display value="NK-cell enteropathy" />
      </concept>
      <concept>
        <code value="ORPHA:2637" />
        <display value="Microcephalic osteodysplastic primordial dwarfism type II" />
      </concept>
      <concept>
        <code value="ORPHA:263708" />
        <display value="Complex chromosomal rearrangement" />
      </concept>
      <concept>
        <code value="ORPHA:263714" />
        <display value="X chromosome number anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:263717" />
        <display value="X chromosome number anomaly with female phenotype" />
      </concept>
      <concept>
        <code value="ORPHA:263720" />
        <display value="X chromosome number anomaly with male phenotype" />
      </concept>
      <concept>
        <code value="ORPHA:263723" />
        <display value="Polysomy of X chromosome" />
      </concept>
      <concept>
        <code value="ORPHA:263726" />
        <display value="Partial deletion of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:263731" />
        <display value="Partial monosomy of the short arm of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:263746" />
        <display value="Y chromosome number anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:263749" />
        <display value="X and Y chromosomal anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:263756" />
        <display value="Partial deletion of the long arm of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:263768" />
        <display value="Partial duplication of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:263775" />
        <display value="Partial duplication of the short arm of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:263783" />
        <display value="Partial duplication of the long arm of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:263793" />
        <display value="Uniparental disomy of chromosome X" />
      </concept>
      <concept>
        <code value="ORPHA:2639" />
        <display value="Fibular aplasia-complex brachydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:264" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy type 1B" />
      </concept>
      <concept>
        <code value="ORPHA:264200" />
        <display value="14q22q23 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2643" />
        <display value="Microcephalic primordial dwarfism, Toriello type" />
      </concept>
      <concept>
        <code value="ORPHA:264431" />
        <display value="Partial duplication of the short arm of chromosome 1" />
      </concept>
      <concept>
        <code value="ORPHA:264450" />
        <display value="Trisomy 8p" />
      </concept>
      <concept>
        <code value="ORPHA:2645" />
        <display value="Osteoglosphonic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:264580" />
        <display value="Glycogen storage disease due to liver phosphorylase kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2646" />
        <display value="Parastremmatic dwarfism" />
      </concept>
      <concept>
        <code value="ORPHA:264656" />
        <display value="Interstitial lung disease specific to childhood" />
      </concept>
      <concept>
        <code value="ORPHA:264665" />
        <display value="Primary interstitial lung disease specific to childhood" />
      </concept>
      <concept>
        <code value="ORPHA:264670" />
        <display value="Primary interstitial lung disease specific to childhood due to alveolar structure disorder" />
      </concept>
      <concept>
        <code value="ORPHA:264675" />
        <display value="Hereditary pulmonary alveolar proteinosis" />
      </concept>
      <concept>
        <code value="ORPHA:264683" />
        <display value="Primary interstitial lung disease specific to childhood due to alveolar vascular disorder" />
      </concept>
      <concept>
        <code value="ORPHA:264688" />
        <display value="Congenital chylothorax" />
      </concept>
      <concept>
        <code value="ORPHA:264691" />
        <display value="Isolated pulmonary capillaritis" />
      </concept>
      <concept>
        <code value="ORPHA:264694" />
        <display value="Interstitial lung disease specific to infancy" />
      </concept>
      <concept>
        <code value="ORPHA:264699" />
        <display value="Secondary interstitial lung disease specific to childhood associated with a systemic disease" />
      </concept>
      <concept>
        <code value="ORPHA:264704" />
        <display value="Secondary interstitial lung disease specific to childhood associated with a connective tissue disease" />
      </concept>
      <concept>
        <code value="ORPHA:264709" />
        <display value="Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:264714" />
        <display value="Secondary interstitial lung disease specific to childhood associated with a granulomatous disease" />
      </concept>
      <concept>
        <code value="ORPHA:264719" />
        <display value="Secondary interstitial lung disease specific to childhood associated with a metabolic disease" />
      </concept>
      <concept>
        <code value="ORPHA:264724" />
        <display value="Langerhans cell histiocytosis specific to childhood" />
      </concept>
      <concept>
        <code value="ORPHA:264735" />
        <display value="Interstitial lung disease specific to adulthood" />
      </concept>
      <concept>
        <code value="ORPHA:264740" />
        <display value="Primary interstitial lung disease specific to adulthood" />
      </concept>
      <concept>
        <code value="ORPHA:264745" />
        <display value="Secondary interstitial lung disease specific to adulthood associated with a systemic disease" />
      </concept>
      <concept>
        <code value="ORPHA:264750" />
        <display value="Langerhans cell histiocytosis specific to adulthood" />
      </concept>
      <concept>
        <code value="ORPHA:264757" />
        <display value="Interstitial lung disease in childhood and adulthood" />
      </concept>
      <concept>
        <code value="ORPHA:264762" />
        <display value="Primary interstitial lung disease in childhood and adulthood" />
      </concept>
      <concept>
        <code value="ORPHA:264930" />
        <display value="Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder" />
      </concept>
      <concept>
        <code value="ORPHA:264935" />
        <display value="Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder" />
      </concept>
      <concept>
        <code value="ORPHA:264944" />
        <display value="Secondary interstitial lung disease in childhood and adulthood" />
      </concept>
      <concept>
        <code value="ORPHA:264949" />
        <display value="Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease" />
      </concept>
      <concept>
        <code value="ORPHA:264955" />
        <display value="Langerhans cell histiocytosis in childhood and adulthood" />
      </concept>
      <concept>
        <code value="ORPHA:264968" />
        <display value="Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease" />
      </concept>
      <concept>
        <code value="ORPHA:264973" />
        <display value="Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:264978" />
        <display value="Drug or radiation exposure-related interstitial lung disease" />
      </concept>
      <concept>
        <code value="ORPHA:264984" />
        <display value="Exposure-related interstitial lung disease" />
      </concept>
      <concept>
        <code value="ORPHA:264992" />
        <display value="Genetic interstitial lung disease" />
      </concept>
      <concept>
        <code value="ORPHA:265" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy type 1C" />
      </concept>
      <concept>
        <code value="ORPHA:2653" />
        <display value="Osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2655" />
        <display value="Thanatophoric dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2658" />
        <display value="Lenz-Majewski hyperostotic dwarfism" />
      </concept>
      <concept>
        <code value="ORPHA:266" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy type 1A" />
      </concept>
      <concept>
        <code value="ORPHA:2662" />
        <display value="Keipert syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2663" />
        <display value="Nathalie syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2665" />
        <display value="Congenital mesoblastic nephroma" />
      </concept>
      <concept>
        <code value="ORPHA:2666" />
        <display value="Adult familial nephronophthisis-spastic quadriparesia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2668" />
        <display value="Nephropathy-deafness-hyperparathyroidism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2669" />
        <display value="Nephrosis-deafness-urinary tract-digital malformations syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:267" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2A" />
      </concept>
      <concept>
        <code value="ORPHA:2670" />
        <display value="Pierson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2671" />
        <display value="Neu-Laxova syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2673" />
        <display value="Neurofaciodigitorenal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2674" />
        <display value="Cyprus facial-neuromusculoskeletal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2676" />
        <display value="Neuroectodermal-endocrine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2677" />
        <display value="Neuroepithelioma" />
      </concept>
      <concept>
        <code value="ORPHA:2678" />
        <display value="Neurofibromatosis type 6" />
      </concept>
      <concept>
        <code value="ORPHA:2679" />
        <display value="Infantile axonal neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:26790" />
        <display value="Pseudomyxoma peritonei" />
      </concept>
      <concept>
        <code value="ORPHA:26791" />
        <display value="Multiple acyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:26792" />
        <display value="Short chain acyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:26793" />
        <display value="Very long chain acyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:268" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2B" />
      </concept>
      <concept>
        <code value="ORPHA:2680" />
        <display value="Hypomyelination neuropathy-arthrogryposis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:268114" />
        <display value="RAS-associated autoimmune leukoproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:268129" />
        <display value="Spheroid body myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:268139" />
        <display value="Intraocular medulloepithelioma" />
      </concept>
      <concept>
        <code value="ORPHA:268145" />
        <display value="Classic maple syrup urine disease" />
      </concept>
      <concept>
        <code value="ORPHA:268162" />
        <display value="Intermediate maple syrup urine disease" />
      </concept>
      <concept>
        <code value="ORPHA:268173" />
        <display value="Intermittent maple syrup urine disease" />
      </concept>
      <concept>
        <code value="ORPHA:268184" />
        <display value="Thiamine-responsive maple syrup urine disease" />
      </concept>
      <concept>
        <code value="ORPHA:268249" />
        <display value="Mycophenolate mofetil embryopathy" />
      </concept>
      <concept>
        <code value="ORPHA:268261" />
        <display value="DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:268322" />
        <display value="Hereditary thrombocytopenia with normal platelets" />
      </concept>
      <concept>
        <code value="ORPHA:268337" />
        <display value="Autosomal recessive intermediate Charcot-Marie-Tooth disease" />
      </concept>
      <concept>
        <code value="ORPHA:268357" />
        <display value="Neural tube closure defect" />
      </concept>
      <concept>
        <code value="ORPHA:268363" />
        <display value="Open iniencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:268366" />
        <display value="Closed iniencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:268369" />
        <display value="Spina bifida aperta" />
      </concept>
      <concept>
        <code value="ORPHA:268377" />
        <display value="Total spina bifida aperta" />
      </concept>
      <concept>
        <code value="ORPHA:268384" />
        <display value="Thoracolumbosacral spina bifida aperta" />
      </concept>
      <concept>
        <code value="ORPHA:268388" />
        <display value="Lumbosacral spina bifida aperta" />
      </concept>
      <concept>
        <code value="ORPHA:268392" />
        <display value="Cervical spina bifida aperta" />
      </concept>
      <concept>
        <code value="ORPHA:268397" />
        <display value="Cervicothoracic spina bifida aperta" />
      </concept>
      <concept>
        <code value="ORPHA:2686" />
        <display value="Cyclic neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:268740" />
        <display value="Upper thoracic spina bifida aperta" />
      </concept>
      <concept>
        <code value="ORPHA:268744" />
        <display value="Spina bifida cystica" />
      </concept>
      <concept>
        <code value="ORPHA:268748" />
        <display value="Total spina bifida cystica" />
      </concept>
      <concept>
        <code value="ORPHA:268752" />
        <display value="Thoracolumbosacral spina bifida cystica" />
      </concept>
      <concept>
        <code value="ORPHA:268758" />
        <display value="Lumbosacral spina bifida cystica" />
      </concept>
      <concept>
        <code value="ORPHA:268762" />
        <display value="Cervical spina bifida cystica" />
      </concept>
      <concept>
        <code value="ORPHA:268766" />
        <display value="Cervicothoracic spina bifida cystica" />
      </concept>
      <concept>
        <code value="ORPHA:268770" />
        <display value="Upper thoracic spina bifida cystica" />
      </concept>
      <concept>
        <code value="ORPHA:2688" />
        <display value="Adult idiopathic neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:268810" />
        <display value="Posterior meningocele" />
      </concept>
      <concept>
        <code value="ORPHA:268813" />
        <display value="Myelocystocele" />
      </concept>
      <concept>
        <code value="ORPHA:268817" />
        <display value="Cephalocele" />
      </concept>
      <concept>
        <code value="ORPHA:268820" />
        <display value="Cranial meningocele" />
      </concept>
      <concept>
        <code value="ORPHA:268823" />
        <display value="Occipital encephalocele" />
      </concept>
      <concept>
        <code value="ORPHA:268826" />
        <display value="Parietal encephalocele" />
      </concept>
      <concept>
        <code value="ORPHA:268829" />
        <display value="Basal encephalocele" />
      </concept>
      <concept>
        <code value="ORPHA:268832" />
        <display value="Lipoma associated with neurospinal dysraphism" />
      </concept>
      <concept>
        <code value="ORPHA:268835" />
        <display value="Lipomyelomeningocele" />
      </concept>
      <concept>
        <code value="ORPHA:268838" />
        <display value="Leptomyelolipoma" />
      </concept>
      <concept>
        <code value="ORPHA:268843" />
        <display value="Malformation of the neurenteric canal, spinal cord and column" />
      </concept>
      <concept>
        <code value="ORPHA:268861" />
        <display value="Primary tethered cord syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:268865" />
        <display value="Neurenteric cyst" />
      </concept>
      <concept>
        <code value="ORPHA:268868" />
        <display value="Isolated amyelia" />
      </concept>
      <concept>
        <code value="ORPHA:268882" />
        <display value="Arnold-Chiari malformation type I" />
      </concept>
      <concept>
        <code value="ORPHA:268920" />
        <display value="Isolated megalencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:268926" />
        <display value="Midline cerebral malformation" />
      </concept>
      <concept>
        <code value="ORPHA:268936" />
        <display value="Isolated arhinencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:268940" />
        <display value="Bilateral polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:268943" />
        <display value="Unilateral polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:268947" />
        <display value="Unilateral focal polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:268950" />
        <display value="Cerebral cortical dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:268961" />
        <display value="Isolated focal cortical dysplasia type I" />
      </concept>
      <concept>
        <code value="ORPHA:268973" />
        <display value="Isolated focal cortical dysplasia type Ia" />
      </concept>
      <concept>
        <code value="ORPHA:268980" />
        <display value="Isolated focal cortical dysplasia type Ib" />
      </concept>
      <concept>
        <code value="ORPHA:268987" />
        <display value="Isolated focal cortical dysplasia type Ic" />
      </concept>
      <concept>
        <code value="ORPHA:268994" />
        <display value="Isolated focal cortical dysplasia type II" />
      </concept>
      <concept>
        <code value="ORPHA:269" />
        <display value="Facioscapulohumeral dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2690" />
        <display value="Neutropenia-monocytopenia-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:269001" />
        <display value="Isolated focal cortical dysplasia type IIa" />
      </concept>
      <concept>
        <code value="ORPHA:269008" />
        <display value="Isolated focal cortical dysplasia type IIb" />
      </concept>
      <concept>
        <code value="ORPHA:269190" />
        <display value="Encephaloclastic disorder" />
      </concept>
      <concept>
        <code value="ORPHA:269194" />
        <display value="Central nervous system cystic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:269197" />
        <display value="Glioependymal/ependymal cyst" />
      </concept>
      <concept>
        <code value="ORPHA:269200" />
        <display value="Retrocerebellar cyst" />
      </concept>
      <concept>
        <code value="ORPHA:269203" />
        <display value="Isolated cerebellar vermis agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:269206" />
        <display value="Isolated total cerebellar vermis agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:269209" />
        <display value="Isolated partial cerebellar vermis agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:269212" />
        <display value="Isolated Dandy-Walker malformation with hydrocephalus" />
      </concept>
      <concept>
        <code value="ORPHA:269215" />
        <display value="Isolated Dandy-Walker malformation without hydrocephalus" />
      </concept>
      <concept>
        <code value="ORPHA:269218" />
        <display value="Isolated unilateral hemispheric cerebellar hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:269221" />
        <display value="Isolated bilateral hemispheric cerebellar hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:269224" />
        <display value="Global cerebellar malformation" />
      </concept>
      <concept>
        <code value="ORPHA:269229" />
        <display value="Pontine tegmental cap dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2695" />
        <display value="Bifid nose" />
      </concept>
      <concept>
        <code value="ORPHA:269505" />
        <display value="Congenital communicating hydrocephalus" />
      </concept>
      <concept>
        <code value="ORPHA:269510" />
        <display value="Congenital non-communicating hydrocephalus" />
      </concept>
      <concept>
        <code value="ORPHA:269523" />
        <display value="Syndrome with a cerebellar malformation as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:269528" />
        <display value="Syndrome with microcephaly as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:269531" />
        <display value="Other syndrome with a central nervous system malformation as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:269546" />
        <display value="Syndrome with a Dandy-Walker malformation as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:269550" />
        <display value="Genetic non-syndromic central nervous system malformation" />
      </concept>
      <concept>
        <code value="ORPHA:269553" />
        <display value="Genetic cerebral malformation" />
      </concept>
      <concept>
        <code value="ORPHA:269557" />
        <display value="Genetic posterior fossa malformation" />
      </concept>
      <concept>
        <code value="ORPHA:269560" />
        <display value="Genetic cerebellar malformation" />
      </concept>
      <concept>
        <code value="ORPHA:269564" />
        <display value="Genetic syndrome with a central nervous system malformation as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:269567" />
        <display value="Genetic syndrome with a cerebellar malformation as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:269570" />
        <display value="Genetic syndrome with a Dandy-Walker malformation as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:269573" />
        <display value="Genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:2697" />
        <display value="Arthrogryposis-renal dysfunction-cholestasis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2698" />
        <display value="Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2699" />
        <display value="Median nodule of the upper lip" />
      </concept>
      <concept>
        <code value="ORPHA:27" />
        <display value="Vitamin B12-unresponsive methylmalonic acidemia" />
      </concept>
      <concept>
        <code value="ORPHA:270" />
        <display value="Oculopharyngeal muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2700" />
        <display value="Noma" />
      </concept>
      <concept>
        <code value="ORPHA:2701" />
        <display value="Noonan syndrome-like disorder with loose anagen hair" />
      </concept>
      <concept>
        <code value="ORPHA:2704" />
        <display value="Ochoa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2707" />
        <display value="Oculocerebrofacial syndrome, Kaufman type" />
      </concept>
      <concept>
        <code value="ORPHA:2709" />
        <display value="Oculodental syndrome, Rutherfurd type" />
      </concept>
      <concept>
        <code value="ORPHA:2710" />
        <display value="Oculodentodigital dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2712" />
        <display value="Oculofaciocardiodental syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2713" />
        <display value="Oculoosteocutaneous syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2714" />
        <display value="Oculo-palato-cerebral syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2715" />
        <display value="Oculorenocerebellar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2717" />
        <display value="Oculotrichoanal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2718" />
        <display value="Oculotrichodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:271832" />
        <display value="Genetic soft tissue tumor" />
      </concept>
      <concept>
        <code value="ORPHA:271835" />
        <display value="Genetic digestive tract tumor" />
      </concept>
      <concept>
        <code value="ORPHA:271841" />
        <display value="Genetic cardiac tumor" />
      </concept>
      <concept>
        <code value="ORPHA:271844" />
        <display value="Genetic urogenital tumor" />
      </concept>
      <concept>
        <code value="ORPHA:271847" />
        <display value="Genetic neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:271853" />
        <display value="Genetic cardiac anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:271861" />
        <display value="Hereditary ATTR amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:271870" />
        <display value="Rare genetic systemic or rheumatologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:2719" />
        <display value="Oculocerebral hypopigmentation syndrome, Cross type" />
      </concept>
      <concept>
        <code value="ORPHA:272" />
        <display value="Congenital muscular dystrophy, Fukuyama type" />
      </concept>
      <concept>
        <code value="ORPHA:2721" />
        <display value="Odonto-onycho-dermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2722" />
        <display value="Odonto-onycho dysplasia-alopecia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2723" />
        <display value="Odontotrichomelic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2724" />
        <display value="Odontomatosis-aortae esophagus stenosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2725" />
        <display value="Eye defects-arachnodactyly-cardiopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2728" />
        <display value="Blepharophimosis-intellectual disability syndrome, Ohdo type" />
      </concept>
      <concept>
        <code value="ORPHA:2729" />
        <display value="Okamoto syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:273" />
        <display value="Steinert myotonic dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2730" />
        <display value="Postaxial tetramelic oligodactyly" />
      </concept>
      <concept>
        <code value="ORPHA:2731" />
        <display value="Taurodontia-absent teeth-sparse hair syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2732" />
        <display value="Olivopontocerebellar atrophy-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2733" />
        <display value="Omodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2736" />
        <display value="Lethal omphalocele-cleft palate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2737" />
        <display value="Onchocerciasis" />
      </concept>
      <concept>
        <code value="ORPHA:274" />
        <display value="Bernard-Soulier syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2741" />
        <display value="Ophthalmomandibulomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2743" />
        <display value="Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2744" />
        <display value="Horizontal gaze palsy with progressive scoliosis" />
      </concept>
      <concept>
        <code value="ORPHA:2745" />
        <display value="Opitz G/BBB syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2746" />
        <display value="Opsismodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:2749" />
        <display value="Oromandibular-limb hypogenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:275" />
        <display value="Severe combined immunodeficiency due to DCLRE1C deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2750" />
        <display value="Orofaciodigital syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:2751" />
        <display value="Orofaciodigital syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:2752" />
        <display value="Orofaciodigital syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:2753" />
        <display value="Orofaciodigital syndrome type 4" />
      </concept>
      <concept>
        <code value="ORPHA:2754" />
        <display value="Orofaciodigital syndrome type 6" />
      </concept>
      <concept>
        <code value="ORPHA:2755" />
        <display value="Orofaciodigital syndrome type 8" />
      </concept>
      <concept>
        <code value="ORPHA:275517" />
        <display value="Autoimmune lymphoproliferative syndrome with recurrent viral infections" />
      </concept>
      <concept>
        <code value="ORPHA:275523" />
        <display value="Dianzani autoimmune lymphoproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:275534" />
        <display value="Myostatin-related muscle hypertrophy" />
      </concept>
      <concept>
        <code value="ORPHA:275543" />
        <display value="L1 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:275555" />
        <display value="Preeclampsia" />
      </concept>
      <concept>
        <code value="ORPHA:2756" />
        <display value="Orofaciodigital syndrome type 10" />
      </concept>
      <concept>
        <code value="ORPHA:275729" />
        <display value="Rare hemorrhagic disorder due to a constitutional thrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:275736" />
        <display value="Rare hemorrhagic disorder due to a qualitative platelet defect" />
      </concept>
      <concept>
        <code value="ORPHA:275742" />
        <display value="Genetic infertility" />
      </concept>
      <concept>
        <code value="ORPHA:275745" />
        <display value="Alpha-thalassemia and related diseases" />
      </concept>
      <concept>
        <code value="ORPHA:275749" />
        <display value="Beta-thalassemia and related diseases" />
      </concept>
      <concept>
        <code value="ORPHA:275752" />
        <display value="Sickle cell disease and related diseases" />
      </concept>
      <concept>
        <code value="ORPHA:275761" />
        <display value="Lysosomal acid lipase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:275766" />
        <display value="Idiopathic pulmonary arterial hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:275777" />
        <display value="Heritable pulmonary arterial hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:275786" />
        <display value="Drug- or toxin-induced pulmonary arterial hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:275791" />
        <display value="Pulmonary arterial hypertension associated with another disease" />
      </concept>
      <concept>
        <code value="ORPHA:275798" />
        <display value="Pulmonary arterial hypertension associated with connective tissue disease" />
      </concept>
      <concept>
        <code value="ORPHA:275803" />
        <display value="Pulmonary arterial hypertension associated with congenital heart disease" />
      </concept>
      <concept>
        <code value="ORPHA:275808" />
        <display value="Pulmonary arterial hypertension associated with HIV infection" />
      </concept>
      <concept>
        <code value="ORPHA:275813" />
        <display value="Pulmonary arterial hypertension associated with portal hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:275823" />
        <display value="Pulmonary arterial hypertension associated with schistosomiasis" />
      </concept>
      <concept>
        <code value="ORPHA:275828" />
        <display value="Pulmonary arterial hypertension associated with chronic hemolytic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:275837" />
        <display value="Pulmonary hypertension owing to lung disease and/or hypoxia" />
      </concept>
      <concept>
        <code value="ORPHA:275844" />
        <display value="Pulmonary hypertension with unclear multifactorial mechanism" />
      </concept>
      <concept>
        <code value="ORPHA:275853" />
        <display value="Syndrome with pulmonary hypertension as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:275864" />
        <display value="Behavioral variant of frontotemporal dementia" />
      </concept>
      <concept>
        <code value="ORPHA:275872" />
        <display value="Frontotemporal dementia with motor neuron disease" />
      </concept>
      <concept>
        <code value="ORPHA:2759" />
        <display value="Imperforate oropharynx-costovertebral anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:275938" />
        <display value="Hemolytic disease due to fetomaternal alloimmunization" />
      </concept>
      <concept>
        <code value="ORPHA:275944" />
        <display value="Hemolytic disease of the newborn with Kell alloimmunization" />
      </concept>
      <concept>
        <code value="ORPHA:276" />
        <display value="T-B+ severe combined immunodeficiency due to gamma chain deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2760" />
        <display value="OSLAM syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:276058" />
        <display value="Genetic neurodegenerative disease with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:276061" />
        <display value="Genetic frontotemporal degeneration with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:276066" />
        <display value="Bile acid CoA ligase deficiency and defective amidation" />
      </concept>
      <concept>
        <code value="ORPHA:276142" />
        <display value="Rare tumor of salivary glands" />
      </concept>
      <concept>
        <code value="ORPHA:276145" />
        <display value="Malignant epithelial tumor of salivary glands" />
      </concept>
      <concept>
        <code value="ORPHA:276148" />
        <display value="Benign epithelial tumor of salivary glands" />
      </concept>
      <concept>
        <code value="ORPHA:276152" />
        <display value="Multiple endocrine neoplasia type 4" />
      </concept>
      <concept>
        <code value="ORPHA:276161" />
        <display value="Multiple endocrine neoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:276174" />
        <display value="Idiopathic recurrent stupor" />
      </concept>
      <concept>
        <code value="ORPHA:276183" />
        <display value="Spinocerebellar ataxia type 32" />
      </concept>
      <concept>
        <code value="ORPHA:276193" />
        <display value="Spinocerebellar ataxia type 35" />
      </concept>
      <concept>
        <code value="ORPHA:276198" />
        <display value="Spinocerebellar ataxia type 36" />
      </concept>
      <concept>
        <code value="ORPHA:2762" />
        <display value="Progressive osseous heteroplasia" />
      </concept>
      <concept>
        <code value="ORPHA:276212" />
        <display value="Mucopolysaccharidosis type 6, rapidly progressing" />
      </concept>
      <concept>
        <code value="ORPHA:276223" />
        <display value="Mucopolysaccharidosis type 6, slowly progressing" />
      </concept>
      <concept>
        <code value="ORPHA:276234" />
        <display value="Non-syndromic male infertility due to sperm motility disorder" />
      </concept>
      <concept>
        <code value="ORPHA:276238" />
        <display value="Machado-Joseph disease type 1" />
      </concept>
      <concept>
        <code value="ORPHA:276241" />
        <display value="Machado-Joseph disease type 2" />
      </concept>
      <concept>
        <code value="ORPHA:276244" />
        <display value="Machado-Joseph disease type 3" />
      </concept>
      <concept>
        <code value="ORPHA:276280" />
        <display value="Hemihyperplasia-multiple lipomatosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2763" />
        <display value="Osteocraniostenosis" />
      </concept>
      <concept>
        <code value="ORPHA:276399" />
        <display value="Familial multinodular goiter" />
      </concept>
      <concept>
        <code value="ORPHA:2764" />
        <display value="Osteochondritis dissecans" />
      </concept>
      <concept>
        <code value="ORPHA:276402" />
        <display value="Limbic encephalitis with caspr2 antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:276405" />
        <display value="Hyperbiliverdinemia" />
      </concept>
      <concept>
        <code value="ORPHA:276413" />
        <display value="10q22.3q23.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:276422" />
        <display value="10q22.3q23.3 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:276429" />
        <display value="Hypnic headache" />
      </concept>
      <concept>
        <code value="ORPHA:276432" />
        <display value="Ogden syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:276435" />
        <display value="Lower motor neuron syndrome with late-adult onset" />
      </concept>
      <concept>
        <code value="ORPHA:276525" />
        <display value="Familial hyperinsulinism" />
      </concept>
      <concept>
        <code value="ORPHA:276556" />
        <display value="Hyperinsulinism due to UCP2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:276575" />
        <display value="Autosomal dominant hyperinsulinism due to SUR1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:276580" />
        <display value="Autosomal dominant hyperinsulinism due to Kir6.2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:276585" />
        <display value="Diazoxide-resistant hyperinsulinism" />
      </concept>
      <concept>
        <code value="ORPHA:276598" />
        <display value="Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:276603" />
        <display value="Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:276608" />
        <display value="Adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia" />
      </concept>
      <concept>
        <code value="ORPHA:276621" />
        <display value="Sporadic pheochromocytoma/secreting paraganglioma" />
      </concept>
      <concept>
        <code value="ORPHA:276624" />
        <display value="Sporadic pheochromocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:276627" />
        <display value="Sporadic secreting paraganglioma" />
      </concept>
      <concept>
        <code value="ORPHA:276630" />
        <display value="Symptomatic form of Coffin-Lowry syndrome in female carriers" />
      </concept>
      <concept>
        <code value="ORPHA:2767" />
        <display value="Carpotarsal osteochondromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:2768" />
        <display value="Blount disease" />
      </concept>
      <concept>
        <code value="ORPHA:2769" />
        <display value="Familial osteodysplasia, Anderson type" />
      </concept>
      <concept>
        <code value="ORPHA:277" />
        <display value="Severe combined immunodeficiency due to adenosine deaminase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2770" />
        <display value="Nasu-Hakola disease" />
      </concept>
      <concept>
        <code value="ORPHA:2771" />
        <display value="Bruck syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2772" />
        <display value="Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2773" />
        <display value="Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2774" />
        <display value="Multicentric carpo-tarsal osteolysis with or without nephropathy" />
      </concept>
      <concept>
        <code value="ORPHA:2776" />
        <display value="Autosomal recessive distal osteolysis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2777" />
        <display value="Osteomesopyknosis" />
      </concept>
      <concept>
        <code value="ORPHA:2779" />
        <display value="Osteopathia striata-pigmentary dermopathy-white forelock syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2780" />
        <display value="Osteopathia striata-cranial sclerosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2781" />
        <display value="Osteopetrosis and related disorders" />
      </concept>
      <concept>
        <code value="ORPHA:2783" />
        <display value="Autosomal dominant osteopetrosis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:2785" />
        <display value="Osteopetrosis with renal tubular acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:2786" />
        <display value="Osteoporosis-oculocutaneous hypopigmentation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2787" />
        <display value="Osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2788" />
        <display value="Osteoporosis-pseudoglioma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2789" />
        <display value="Lateral meningocele syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2790" />
        <display value="Endosteal hyperostosis, Worth type" />
      </concept>
      <concept>
        <code value="ORPHA:2791" />
        <display value="Otodental syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2792" />
        <display value="Otofaciocervical syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2793" />
        <display value="Otoonychoperoneal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2795" />
        <display value="Polycystic ovaries-urethral sphincter dysfunction syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2796" />
        <display value="Pachydermoperiostosis" />
      </concept>
      <concept>
        <code value="ORPHA:2798" />
        <display value="Pachygyria-intellectual disability-epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:279882" />
        <display value="Spasmus nutans" />
      </concept>
      <concept>
        <code value="ORPHA:279888" />
        <display value="Acute endophthalmitis" />
      </concept>
      <concept>
        <code value="ORPHA:279891" />
        <display value="Chronic endophthalmitis" />
      </concept>
      <concept>
        <code value="ORPHA:279894" />
        <display value="Toxic maculopathy due to antimalarial drugs" />
      </concept>
      <concept>
        <code value="ORPHA:279897" />
        <display value="Primary oculocerebral lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:279904" />
        <display value="Primary intraocular lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:279911" />
        <display value="Primary organ-specific lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:279914" />
        <display value="Intermediate uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:279919" />
        <display value="Infectious posterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:279922" />
        <display value="Infectious anterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:279925" />
        <display value="Infectious panuveitis" />
      </concept>
      <concept>
        <code value="ORPHA:279928" />
        <display value="Paraneoplastic uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:279934" />
        <display value="Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:279943" />
        <display value="Hereditary neutrophilia" />
      </concept>
      <concept>
        <code value="ORPHA:279947" />
        <display value="Postorgasmic illness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:28" />
        <display value="Vitamin B12-responsive methylmalonic acidemia" />
      </concept>
      <concept>
        <code value="ORPHA:280" />
        <display value="Wolf-Hirschhorn syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2800" />
        <display value="Extramammary Paget disease" />
      </concept>
      <concept>
        <code value="ORPHA:280062" />
        <display value="Calciphylaxis" />
      </concept>
      <concept>
        <code value="ORPHA:280065" />
        <display value="Calciphylaxis cutis" />
      </concept>
      <concept>
        <code value="ORPHA:280068" />
        <display value="Visceral calciphylaxis" />
      </concept>
      <concept>
        <code value="ORPHA:280071" />
        <display value="ALG11-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:2801" />
        <display value="Juvenile Paget disease" />
      </concept>
      <concept>
        <code value="ORPHA:280133" />
        <display value="Complement component 3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:280142" />
        <display value="Severe combined immunodeficiency due to LCK deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:280183" />
        <display value="Methylmalonic aciduria due to transcobalamin receptor defect" />
      </concept>
      <concept>
        <code value="ORPHA:280195" />
        <display value="Septopreoptic holoprosencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:2802" />
        <display value="X-linked sideroblastic anemia and spinocerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:280200" />
        <display value="Microform holoprosencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:280205" />
        <display value="Laryngotracheoesophageal cleft type 0" />
      </concept>
      <concept>
        <code value="ORPHA:280210" />
        <display value="Pelizaeus-Merzbacher disease, connatal form" />
      </concept>
      <concept>
        <code value="ORPHA:280219" />
        <display value="Pelizaeus-Merzbacher disease, classic form" />
      </concept>
      <concept>
        <code value="ORPHA:280224" />
        <display value="Pelizaeus-Merzbacher disease, transitional form" />
      </concept>
      <concept>
        <code value="ORPHA:280229" />
        <display value="Pelizaeus-Merzbacher disease in female carriers" />
      </concept>
      <concept>
        <code value="ORPHA:280234" />
        <display value="Null syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:280270" />
        <display value="Pelizaeus-Merzbacher-like disease" />
      </concept>
      <concept>
        <code value="ORPHA:280282" />
        <display value="Pelizaeus-Merzbacher-like disease due to GJC2 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:280288" />
        <display value="Pelizaeus-Merzbacher-like disease due to HSPD1 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:280293" />
        <display value="Pelizaeus-Merzbacher-like disease due to AIMP1 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:280302" />
        <display value="Autoimmune pancreatitis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:280315" />
        <display value="Autoimmune pancreatitis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:280325" />
        <display value="Distal monosomy 12p" />
      </concept>
      <concept>
        <code value="ORPHA:280333" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2P" />
      </concept>
      <concept>
        <code value="ORPHA:280342" />
        <display value="Rare systemic or rheumatological disease of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:280356" />
        <display value="PLIN1-related familial partial lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:280365" />
        <display value="Autosomal semi-dominant severe lipodystrophic laminopathy" />
      </concept>
      <concept>
        <code value="ORPHA:280369" />
        <display value="Rare pediatric vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:280373" />
        <display value="Rare pediatric systemic disease" />
      </concept>
      <concept>
        <code value="ORPHA:280379" />
        <display value="Erythropoietic uroporphyria associated with myeloid malignancy" />
      </concept>
      <concept>
        <code value="ORPHA:280384" />
        <display value="Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:280397" />
        <display value="Familial Alzheimer-like prion disease" />
      </concept>
      <concept>
        <code value="ORPHA:2804" />
        <display value="W syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:280400" />
        <display value="Inherited prion disease" />
      </concept>
      <concept>
        <code value="ORPHA:280403" />
        <display value="Familial omphalocele syndrome with facial dysmorphism" />
      </concept>
      <concept>
        <code value="ORPHA:280406" />
        <display value="Familial steroid-resistant nephrotic syndrome with sensorineural deafness" />
      </concept>
      <concept>
        <code value="ORPHA:2805" />
        <display value="Partial pancreatic agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:280553" />
        <display value="Fatal infantile hypertonic myofibrillar myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:280558" />
        <display value="Warsaw breakage syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:280569" />
        <display value="Rapidly progressive glomerulonephritis" />
      </concept>
      <concept>
        <code value="ORPHA:280576" />
        <display value="Nestor-Guillermo progeria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:280586" />
        <display value="Chondrodysplasia with joint dislocations, gPAPP type" />
      </concept>
      <concept>
        <code value="ORPHA:280598" />
        <display value="Hereditary sensorimotor neuropathy with hyperelastic skin" />
      </concept>
      <concept>
        <code value="ORPHA:2806" />
        <display value="Subacute sclerosing leukoencephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:280615" />
        <display value="Hemoglobinopathy Toms River" />
      </concept>
      <concept>
        <code value="ORPHA:280620" />
        <display value="Progressive myoclonic epilepsy type 6" />
      </concept>
      <concept>
        <code value="ORPHA:280628" />
        <display value="Familial progressive hyper- and hypopigmentation" />
      </concept>
      <concept>
        <code value="ORPHA:280633" />
        <display value="Multiple congenital anomalies-hypotonia-seizures syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:280640" />
        <display value="Occipital pachygyria and polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:280651" />
        <display value="Acrodysostosis with multiple hormone resistance" />
      </concept>
      <concept>
        <code value="ORPHA:280654" />
        <display value="Autosomal recessive nail dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:280663" />
        <display value="Hermansky-Pudlak syndrome type 9" />
      </concept>
      <concept>
        <code value="ORPHA:280671" />
        <display value="Megaconial congenital muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:280679" />
        <display value="Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2807" />
        <display value="Papilloma of choroid plexus" />
      </concept>
      <concept>
        <code value="ORPHA:280763" />
        <display value="Severe intellectual disability and progressive spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:280774" />
        <display value="Generalized essential telangiectasia" />
      </concept>
      <concept>
        <code value="ORPHA:280779" />
        <display value="Cutaneous collagenous vasculopathy" />
      </concept>
      <concept>
        <code value="ORPHA:280785" />
        <display value="Bullous diffuse cutaneous mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:280794" />
        <display value="Pseudoxanthomatous diffuse cutaneous mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:2808" />
        <display value="Laryngeal abductor paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:280802" />
        <display value="Intralobar congenital pulmonary sequestration" />
      </concept>
      <concept>
        <code value="ORPHA:280811" />
        <display value="Extralobar congenital pulmonary sequestration" />
      </concept>
      <concept>
        <code value="ORPHA:280821" />
        <display value="Communicating congenital bronchopulmonary-foregut malformation" />
      </concept>
      <concept>
        <code value="ORPHA:280827" />
        <display value="Congenital pulmonary airway malformation type 0" />
      </concept>
      <concept>
        <code value="ORPHA:280832" />
        <display value="Congenital pulmonary airway malformation type 1" />
      </concept>
      <concept>
        <code value="ORPHA:280840" />
        <display value="Congenital pulmonary airway malformation type 2" />
      </concept>
      <concept>
        <code value="ORPHA:280847" />
        <display value="Congenital pulmonary airway malformation type 3" />
      </concept>
      <concept>
        <code value="ORPHA:280854" />
        <display value="Congenital pulmonary airway malformation type 4" />
      </concept>
      <concept>
        <code value="ORPHA:280886" />
        <display value="Anterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:280892" />
        <display value="Posterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:280898" />
        <display value="Panuveitis" />
      </concept>
      <concept>
        <code value="ORPHA:2809" />
        <display value="Familial recurrent peripheral facial palsy" />
      </concept>
      <concept>
        <code value="ORPHA:280914" />
        <display value="Idiopathic anterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:280917" />
        <display value="Idiopathic posterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:280921" />
        <display value="Idiopathic panuveitis" />
      </concept>
      <concept>
        <code value="ORPHA:280926" />
        <display value="Systemic diseases with anterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:280930" />
        <display value="Systemic diseases with posterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:280933" />
        <display value="Systemic diseases with panuveitis" />
      </concept>
      <concept>
        <code value="ORPHA:281" />
        <display value="Monosomy 5p" />
      </concept>
      <concept>
        <code value="ORPHA:281082" />
        <display value="Inherited non-syndromic ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:281085" />
        <display value="Inherited ichthyosis syndromic form" />
      </concept>
      <concept>
        <code value="ORPHA:281090" />
        <display value="Syndromic recessive X-linked ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:281097" />
        <display value="Autosomal recessive congenital ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:281103" />
        <display value="Keratinopathic ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:281122" />
        <display value="Self-improving collodion baby" />
      </concept>
      <concept>
        <code value="ORPHA:281127" />
        <display value="Acral self-healing collodion baby" />
      </concept>
      <concept>
        <code value="ORPHA:281139" />
        <display value="Annular epidermolytic ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:281190" />
        <display value="Congenital reticular ichthyosiform erythroderma" />
      </concept>
      <concept>
        <code value="ORPHA:2812" />
        <display value="Parana hard skin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:281201" />
        <display value="Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:281210" />
        <display value="X-linked ichthyosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:281217" />
        <display value="Autosomal ichthyosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:281222" />
        <display value="Autosomal ichthyosis syndrome with prominent hair abnormalities" />
      </concept>
      <concept>
        <code value="ORPHA:281238" />
        <display value="Autosomal ichthyosis syndrome with prominent neurologic signs" />
      </concept>
      <concept>
        <code value="ORPHA:281241" />
        <display value="Autosomal ichthyosis syndrome with fatal disease course" />
      </concept>
      <concept>
        <code value="ORPHA:281244" />
        <display value="Autosomal ichthyosis syndrome with other associated signs" />
      </concept>
      <concept>
        <code value="ORPHA:2815" />
        <display value="Spastic paraparesis-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2818" />
        <display value="Spastic paraplegia-glaucoma-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2819" />
        <display value="Spastic paraplegia-facial-cutaneous lesions syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:282" />
        <display value="Frontotemporal dementia" />
      </concept>
      <concept>
        <code value="ORPHA:2820" />
        <display value="Spastic paraplegia-nephritis-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2821" />
        <display value="Spastic paraplegia-neuropathy-poikiloderma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:282124" />
        <display value="Partial deletion of chromosome 12" />
      </concept>
      <concept>
        <code value="ORPHA:282166" />
        <display value="Inherited Creutzfeldt-Jakob disease" />
      </concept>
      <concept>
        <code value="ORPHA:282196" />
        <display value="Autoimmune polyendocrinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2822" />
        <display value="Autosomal recessive spastic paraplegia type 11" />
      </concept>
      <concept>
        <code value="ORPHA:2824" />
        <display value="Paraplegia-intellectual disability-hyperkeratosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2825" />
        <display value="PARC syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2826" />
        <display value="Spastic paraplegia-precocious puberty syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2828" />
        <display value="Young-onset Parkinson disease" />
      </concept>
      <concept>
        <code value="ORPHA:283" />
        <display value="Demodicidosis" />
      </concept>
      <concept>
        <code value="ORPHA:2831" />
        <display value="Rhizomelic dysplasia, Patterson-Lowry type" />
      </concept>
      <concept>
        <code value="ORPHA:2832" />
        <display value="Short tarsus-absence of lower eyelashes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2833" />
        <display value="Stiff skin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2834" />
        <display value="Wrinkly skin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2835" />
        <display value="Pectus excavatum-macrocephaly-dysplastic nails syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2836" />
        <display value="PEHO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:28378" />
        <display value="Tyrosinemia type 2" />
      </concept>
      <concept>
        <code value="ORPHA:2838" />
        <display value="Renal caliceal diverticuli-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2839" />
        <display value="Pelvis-shoulder dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:284" />
        <display value="Alveolar echinococcosis" />
      </concept>
      <concept>
        <code value="ORPHA:2840" />
        <display value="Pelvic dysplasia-arthrogryposis of lower limbs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2841" />
        <display value="Familial benign chronic pemphigus" />
      </concept>
      <concept>
        <code value="ORPHA:284139" />
        <display value="Larsen-like syndrome, B3GAT3 type" />
      </concept>
      <concept>
        <code value="ORPHA:284149" />
        <display value="Craniosynostosis-dental anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:284160" />
        <display value="8q21.11 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284169" />
        <display value="Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:284180" />
        <display value="Xp22.13p22.2 duplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2842" />
        <display value="Penoscrotal transposition" />
      </concept>
      <concept>
        <code value="ORPHA:284227" />
        <display value="TEMPI syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284232" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2O" />
      </concept>
      <concept>
        <code value="ORPHA:284247" />
        <display value="Familial retinal arterial macroaneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:284264" />
        <display value="IgG4-related disease" />
      </concept>
      <concept>
        <code value="ORPHA:284271" />
        <display value="Autosomal recessive cerebellar ataxia-psychomotor retardation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284282" />
        <display value="Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:284289" />
        <display value="Adult-onset autosomal recessive cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:2843" />
        <display value="Pentosuria" />
      </concept>
      <concept>
        <code value="ORPHA:284324" />
        <display value="Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:284332" />
        <display value="Infantile-onset autosomal recessive nonprogressive cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:284339" />
        <display value="Pontocerebellar hypoplasia type 7" />
      </concept>
      <concept>
        <code value="ORPHA:284343" />
        <display value="Pleuropulmonary blastoma familial tumor susceptibility syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284362" />
        <display value="Fetal lung interstitial tumor" />
      </concept>
      <concept>
        <code value="ORPHA:284385" />
        <display value="Familial intrahepatic cholestasis" />
      </concept>
      <concept>
        <code value="ORPHA:284388" />
        <display value="Reversible cerebral vasoconstriction syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284395" />
        <display value="Well-differentiated fetal adenocarcinoma of the lung" />
      </concept>
      <concept>
        <code value="ORPHA:284400" />
        <display value="Small cell carcinoma of the bladder" />
      </concept>
      <concept>
        <code value="ORPHA:284408" />
        <display value="Glycerol kinase deficiency, infantile form" />
      </concept>
      <concept>
        <code value="ORPHA:284411" />
        <display value="Glycerol kinase deficiency, juvenile form" />
      </concept>
      <concept>
        <code value="ORPHA:284414" />
        <display value="Glycerol kinase deficiency, adult form" />
      </concept>
      <concept>
        <code value="ORPHA:284417" />
        <display value="Phosphoserine aminotransferase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:284426" />
        <display value="Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:284435" />
        <display value="Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:284448" />
        <display value="CLIPPERS" />
      </concept>
      <concept>
        <code value="ORPHA:284454" />
        <display value="Acute zonal occult outer retinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:284460" />
        <display value="Acute annular outer retinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2846" />
        <display value="Congenital pericardium anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:2847" />
        <display value="Pericardial and diaphragmatic defect" />
      </concept>
      <concept>
        <code value="ORPHA:284786" />
        <display value="Qualitative or quantitative defects of troponin" />
      </concept>
      <concept>
        <code value="ORPHA:284790" />
        <display value="Qualitative or quantitative defects of tropomyosin" />
      </concept>
      <concept>
        <code value="ORPHA:2848" />
        <display value="Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284804" />
        <display value="Ocular albinism" />
      </concept>
      <concept>
        <code value="ORPHA:284811" />
        <display value="Syndromic oculocutaneous albinism" />
      </concept>
      <concept>
        <code value="ORPHA:284814" />
        <display value="Disorder of phenylalanine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:284818" />
        <display value="Disorder of tyrosine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:2849" />
        <display value="Perlman syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284963" />
        <display value="Marfan syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:284973" />
        <display value="Marfan syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:284979" />
        <display value="Neonatal Marfan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284984" />
        <display value="Aneurysm-osteoarthritis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:284993" />
        <display value="Marfan and Marfan-related disorder" />
      </concept>
      <concept>
        <code value="ORPHA:285" />
        <display value="Ehlers-Danlos syndrome, hypermobility type" />
      </concept>
      <concept>
        <code value="ORPHA:2850" />
        <display value="Alopecia-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:285014" />
        <display value="Rare disease with thoracic aortic aneurysm and aortic dissection" />
      </concept>
      <concept>
        <code value="ORPHA:2854" />
        <display value="Fuhrmann syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2855" />
        <display value="Perrault syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2856" />
        <display value="Persistent Mullerian duct syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:285657" />
        <display value="Disorder of folate metabolism and transport" />
      </concept>
      <concept>
        <code value="ORPHA:286" />
        <display value="Ehlers-Danlos syndrome, vascular type" />
      </concept>
      <concept>
        <code value="ORPHA:2863" />
        <display value="Short stature-wormian bones-dextrocardia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2865" />
        <display value="Short stature-webbed neck-heart disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2866" />
        <display value="Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2867" />
        <display value="Short stature, Brussels type" />
      </concept>
      <concept>
        <code value="ORPHA:2868" />
        <display value="Short stature-valvular heart disease-characteristic facies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2869" />
        <display value="Peutz-Jeghers syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:287" />
        <display value="Ehlers-Danlos syndrome, classic type" />
      </concept>
      <concept>
        <code value="ORPHA:2871" />
        <display value="Pfeiffer-Palm-Teller syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2872" />
        <display value="Cardiocranial syndrome, Pfeiffer type" />
      </concept>
      <concept>
        <code value="ORPHA:2874" />
        <display value="Phakomatosis pigmentokeratotica" />
      </concept>
      <concept>
        <code value="ORPHA:2875" />
        <display value="Phakomatosis pigmentovascularis" />
      </concept>
      <concept>
        <code value="ORPHA:2876" />
        <display value="PHAVER syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2878" />
        <display value="Phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2879" />
        <display value="Phocomelia, Schinzel type" />
      </concept>
      <concept>
        <code value="ORPHA:288" />
        <display value="Hereditary elliptocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:2880" />
        <display value="Phosphoenolpyruvate carboxykinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2881" />
        <display value="Cutaneous photosensitivity-lethal colitis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2882" />
        <display value="Sitosterolemia" />
      </concept>
      <concept>
        <code value="ORPHA:2884" />
        <display value="Piebaldism" />
      </concept>
      <concept>
        <code value="ORPHA:2885" />
        <display value="Piebald trait-neurologic defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2886" />
        <display value="TARP syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2888" />
        <display value="Pierre Robin syndrome-faciodigital anomaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2889" />
        <display value="Pili torti" />
      </concept>
      <concept>
        <code value="ORPHA:289" />
        <display value="Ellis Van Creveld syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2890" />
        <display value="Pili torti-onychodysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289098" />
        <display value="Disorders of vitamin D metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:2891" />
        <display value="Pili torti-developmental delay-neurological abnormalities syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289103" />
        <display value="Hypocalcemic rickets" />
      </concept>
      <concept>
        <code value="ORPHA:289157" />
        <display value="Hypocalcemic vitamin D-dependent rickets" />
      </concept>
      <concept>
        <code value="ORPHA:289176" />
        <display value="Autosomal recessive hypophosphatemic rickets" />
      </concept>
      <concept>
        <code value="ORPHA:2892" />
        <display value="Pilodental dysplasia-refractive errors syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289266" />
        <display value="Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation" />
      </concept>
      <concept>
        <code value="ORPHA:289290" />
        <display value="Hypermethioninemia encephalopathy due to adenosine kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:289307" />
        <display value="Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:289326" />
        <display value="Tropical spastic paraparesis" />
      </concept>
      <concept>
        <code value="ORPHA:289347" />
        <display value="Infective dermatitis associated with HTLV-1" />
      </concept>
      <concept>
        <code value="ORPHA:289356" />
        <display value="Primary non-gestational choriocarcinoma of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:289362" />
        <display value="Non-central nervous system-localized embryonal carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:289365" />
        <display value="Familial vesicoureteral reflux" />
      </concept>
      <concept>
        <code value="ORPHA:289377" />
        <display value="Early-onset myopathy with fatal cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:289380" />
        <display value="Myosclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:289385" />
        <display value="Malignancy diagnosed during pregnancy" />
      </concept>
      <concept>
        <code value="ORPHA:289390" />
        <display value="Primary Sjogren syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289465" />
        <display value="Isolated congenital adermatoglyphia" />
      </concept>
      <concept>
        <code value="ORPHA:289478" />
        <display value="Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289483" />
        <display value="Intellectual disability-alacrima-achalasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289494" />
        <display value="Hypomyelinating leukodystrophy with or without oligondontia and/or hypogonadism" />
      </concept>
      <concept>
        <code value="ORPHA:289499" />
        <display value="Congenital cataract microcornea with corneal opacity" />
      </concept>
      <concept>
        <code value="ORPHA:289504" />
        <display value="Combined malonic and methylmalonic acidemia" />
      </concept>
      <concept>
        <code value="ORPHA:289513" />
        <display value="12q15q21.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289522" />
        <display value="Microtriplication 11q24.1" />
      </concept>
      <concept>
        <code value="ORPHA:289527" />
        <display value="Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:289539" />
        <display value="BAP1-related tumor predisposition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289548" />
        <display value="Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:289553" />
        <display value="Dysmorphism-conductive hearing loss-heart defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289560" />
        <display value="Mitochondrial membrane protein-associated neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:289573" />
        <display value="Multiple mitochondrial dysfunctions syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289586" />
        <display value="Exfoliative ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:289596" />
        <display value="Juvenile nasopharyngeal angiofibroma" />
      </concept>
      <concept>
        <code value="ORPHA:2896" />
        <display value="Pitt-Hopkins syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289601" />
        <display value="Hereditary arterial and articular multiple calcification syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289635" />
        <display value="Rare virus associated tumor" />
      </concept>
      <concept>
        <code value="ORPHA:289638" />
        <display value="Epstein-Barr Virus-related tumor" />
      </concept>
      <concept>
        <code value="ORPHA:289644" />
        <display value="Epstein-Barr virus-associated malignant lymphoproliferative disorder" />
      </concept>
      <concept>
        <code value="ORPHA:289651" />
        <display value="Epstein-Barr Virus-associated carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:289656" />
        <display value="Epstein-Barr Virus-associated mesenchymal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:289661" />
        <display value="Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly" />
      </concept>
      <concept>
        <code value="ORPHA:289666" />
        <display value="Plasmablastic lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:289682" />
        <display value="Lymphoepithelial-like carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:289685" />
        <display value="Myopericytoma" />
      </concept>
      <concept>
        <code value="ORPHA:2897" />
        <display value="Pityriasis rubra pilaris" />
      </concept>
      <concept>
        <code value="ORPHA:2898" />
        <display value="X-linked intellectual disability-plagiocephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289829" />
        <display value="Disorder of tryptophan metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:289832" />
        <display value="Disorder of lysine and hydroxylysine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:289841" />
        <display value="Disorder of glutamine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:289846" />
        <display value="Glutathione synthetase deficiency with 5-oxoprolinuria" />
      </concept>
      <concept>
        <code value="ORPHA:289849" />
        <display value="Glutathione synthetase deficiency without 5-oxoprolinuria" />
      </concept>
      <concept>
        <code value="ORPHA:289857" />
        <display value="Neonatal glycine encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:289860" />
        <display value="Infantile glycine encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:289863" />
        <display value="Atypical glycine encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:289866" />
        <display value="Disorder of proline metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:289869" />
        <display value="Disorder of ornithine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:289877" />
        <display value="Transient hyperammonemia of the newborn" />
      </concept>
      <concept>
        <code value="ORPHA:289891" />
        <display value="Hypermethioninemia due to glycine N-methyltransferase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:289899" />
        <display value="Organic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:2899" />
        <display value="Brachyolmia-amelogenesis imperfecta syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:289902" />
        <display value="3-methylglutaconic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:289916" />
        <display value="Vitamin B12-unresponsive methylmalonic acidemia type mut0" />
      </concept>
      <concept>
        <code value="ORPHA:29" />
        <display value="Mevalonic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:290" />
        <display value="Congenital rubella syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2900" />
        <display value="Leri pleonosteosis" />
      </concept>
      <concept>
        <code value="ORPHA:2901" />
        <display value="Neuralgic amyotrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2902" />
        <display value="Idiopathic chronic eosinophilic pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:2903" />
        <display value="Familial spontaneous pneumothorax" />
      </concept>
      <concept>
        <code value="ORPHA:2905" />
        <display value="POEMS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2907" />
        <display value="Hereditary acrokeratotic poikiloderma, Weary type" />
      </concept>
      <concept>
        <code value="ORPHA:29072" />
        <display value="Hereditary pheochromocytoma-paraganglioma" />
      </concept>
      <concept>
        <code value="ORPHA:29073" />
        <display value="Multiple myeloma" />
      </concept>
      <concept>
        <code value="ORPHA:2908" />
        <display value="Kindler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:290836" />
        <display value="Systemic disease with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:290839" />
        <display value="Autoinflammatory syndrome with immune deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:290842" />
        <display value="Autoinflammatory syndrome with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:290849" />
        <display value="Rare head and neck tumor" />
      </concept>
      <concept>
        <code value="ORPHA:2909" />
        <display value="Rothmund-Thomson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:291" />
        <display value="Congenital varicella syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2911" />
        <display value="Poland syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2912" />
        <display value="Poliomyelitis" />
      </concept>
      <concept>
        <code value="ORPHA:2913" />
        <display value="Non-syndromic polydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:2916" />
        <display value="Postaxial polydactyly-dental and vertebral anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2917" />
        <display value="Polydactyly-myopia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2919" />
        <display value="Orofaciodigital syndrome type 5" />
      </concept>
      <concept>
        <code value="ORPHA:292" />
        <display value="Congenital enterovirus infection" />
      </concept>
      <concept>
        <code value="ORPHA:2920" />
        <display value="Oliver syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:29207" />
        <display value="Reactive arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:2921" />
        <display value="Preaxial polydactyly-colobomata-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2924" />
        <display value="Isolated polycystic liver disease" />
      </concept>
      <concept>
        <code value="ORPHA:2926" />
        <display value="Digital extensor muscle aplasia-polyneuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:2928" />
        <display value="Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2929" />
        <display value="Juvenile polyposis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293" />
        <display value="Congenital herpes simplex virus infection" />
      </concept>
      <concept>
        <code value="ORPHA:2930" />
        <display value="Cronkhite-Canada syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293144" />
        <display value="Familial clubfoot due to 5q31 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:293150" />
        <display value="Familial clubfoot due to PITX1 point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:293165" />
        <display value="Skin fragility-woolly hair-palmoplantar keratoderma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293168" />
        <display value="Infantile-onset ascending hereditary spastic paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:293173" />
        <display value="Acute generalized exanthematous pustulosis" />
      </concept>
      <concept>
        <code value="ORPHA:293181" />
        <display value="Malignant migrating partial seizures of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:293199" />
        <display value="Pleomorphic rhabdomyosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:2932" />
        <display value="Chronic inflammatory demyelinating polyneuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:293202" />
        <display value="Epithelioid sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:293208" />
        <display value="Celiac artery compression syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293284" />
        <display value="Tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria" />
      </concept>
      <concept>
        <code value="ORPHA:293355" />
        <display value="Methylmalonic acidemia without homocystinuria" />
      </concept>
      <concept>
        <code value="ORPHA:293375" />
        <display value="Grayson-Wilbrandt corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:293381" />
        <display value="Epithelial recurrent erosion dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2934" />
        <display value="Polysyndactyly-cardiac malformation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293462" />
        <display value="Pre-Descemet corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2935" />
        <display value="Crossed polysyndactyly" />
      </concept>
      <concept>
        <code value="ORPHA:293603" />
        <display value="Congenital hereditary endothelial dystrophy type II" />
      </concept>
      <concept>
        <code value="ORPHA:293621" />
        <display value="X-linked endothelial corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:293633" />
        <display value="PYCR1-related De Barsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293642" />
        <display value="Blepharophimosis-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293707" />
        <display value="Blepharophimosis-intellectual disability syndrome, MKB type" />
      </concept>
      <concept>
        <code value="ORPHA:293725" />
        <display value="Blepharophimosis-intellectual disability syndrome, Verloes type" />
      </concept>
      <concept>
        <code value="ORPHA:293807" />
        <display value="Ketamine-induced biliary dilatation" />
      </concept>
      <concept>
        <code value="ORPHA:293812" />
        <display value="Fixed drug eruption" />
      </concept>
      <concept>
        <code value="ORPHA:293815" />
        <display value="Toxic dermatosis" />
      </concept>
      <concept>
        <code value="ORPHA:293822" />
        <display value="MITF-related melanoma and renal cell carcinoma predisposition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293825" />
        <display value="Congenital dyserythropoietic anemia type IV" />
      </concept>
      <concept>
        <code value="ORPHA:293830" />
        <display value="Constitutional dyserythropoietic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:293843" />
        <display value="3MC syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293848" />
        <display value="Frontotemporal dementia, right temporal atrophy variant" />
      </concept>
      <concept>
        <code value="ORPHA:293864" />
        <display value="Hypoplastic pancreas-intestinal atresia-hypoplastic gallbladder syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293888" />
        <display value="Familial isolated arrhythmogenic ventricular dysplasia, left dominant form" />
      </concept>
      <concept>
        <code value="ORPHA:293899" />
        <display value="Familial isolated arrhythmogenic ventricular dysplasia, biventricular form" />
      </concept>
      <concept>
        <code value="ORPHA:293910" />
        <display value="Familial isolated arrhythmogenic ventricular dysplasia, right dominant form" />
      </concept>
      <concept>
        <code value="ORPHA:293925" />
        <display value="Lethal occipital encephalocele-skeletal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293936" />
        <display value="EDICT syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293939" />
        <display value="Distal Xq28 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293948" />
        <display value="1p21.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293955" />
        <display value="Childhood encephalopathy due to thiamine pyrophosphokinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:293958" />
        <display value="Hypertelorism-preauricular sinus-punctual pits-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293964" />
        <display value="Hypoinsulinemic hypoglycemia and body hemihypertrophy" />
      </concept>
      <concept>
        <code value="ORPHA:293967" />
        <display value="Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293978" />
        <display value="Deficiency in anterior pituitary function-variable immunodeficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:293987" />
        <display value="Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:294" />
        <display value="Fetal cytomegalovirus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2940" />
        <display value="Porencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:294016" />
        <display value="Microcephaly-capillary malformation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:294023" />
        <display value="Neonatal inflammatory skin and bowel disease" />
      </concept>
      <concept>
        <code value="ORPHA:294026" />
        <display value="2q31.1 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:294049" />
        <display value="Reunion Island Larsen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:294057" />
        <display value="Rare nevus" />
      </concept>
      <concept>
        <code value="ORPHA:294060" />
        <display value="Multiple pterygium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2941" />
        <display value="Porencephaly-cerebellar hypoplasia-internal malformations syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2942" />
        <display value="Postpoliomyelitis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:294415" />
        <display value="Renal-hepatic-pancreatic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:294422" />
        <display value="Chronic intestinal failure" />
      </concept>
      <concept>
        <code value="ORPHA:2946" />
        <display value="Brachydactyly-long thumb syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2947" />
        <display value="Triphalangeal thumbs-brachyectrodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:294925" />
        <display value="Amelia" />
      </concept>
      <concept>
        <code value="ORPHA:294927" />
        <display value="Intercalary limb defects" />
      </concept>
      <concept>
        <code value="ORPHA:294944" />
        <display value="Congenital deformities of limbs" />
      </concept>
      <concept>
        <code value="ORPHA:294947" />
        <display value="Congenital deformities of fingers" />
      </concept>
      <concept>
        <code value="ORPHA:294949" />
        <display value="Joint formation defects" />
      </concept>
      <concept>
        <code value="ORPHA:294951" />
        <display value="Congenital joint dislocations" />
      </concept>
      <concept>
        <code value="ORPHA:294953" />
        <display value="Limb overgrowth" />
      </concept>
      <concept>
        <code value="ORPHA:294955" />
        <display value="Syndrome with limb reduction defects" />
      </concept>
      <concept>
        <code value="ORPHA:294957" />
        <display value="Dysostosis with combined reduction defects of upper and lower limbs" />
      </concept>
      <concept>
        <code value="ORPHA:294959" />
        <display value="Syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy" />
      </concept>
      <concept>
        <code value="ORPHA:294963" />
        <display value="Popliteal pterygium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:294965" />
        <display value="Lethal congenital contracture syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:294967" />
        <display value="Amelia of upper limb" />
      </concept>
      <concept>
        <code value="ORPHA:294969" />
        <display value="Amelia of lower limb" />
      </concept>
      <concept>
        <code value="ORPHA:294971" />
        <display value="Tetra-amelia" />
      </concept>
      <concept>
        <code value="ORPHA:294973" />
        <display value="Humeral agenesis/hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:294975" />
        <display value="Congenital absence of upper arm and forearm with hand present" />
      </concept>
      <concept>
        <code value="ORPHA:294977" />
        <display value="Congenital absence of thigh and lower leg with foot present" />
      </concept>
      <concept>
        <code value="ORPHA:294979" />
        <display value="Congenital absence of both forearm and hand" />
      </concept>
      <concept>
        <code value="ORPHA:294981" />
        <display value="Congenital absence of both lower leg and foot" />
      </concept>
      <concept>
        <code value="ORPHA:294983" />
        <display value="Acheiria" />
      </concept>
      <concept>
        <code value="ORPHA:294986" />
        <display value="Apodia" />
      </concept>
      <concept>
        <code value="ORPHA:294988" />
        <display value="Congenital absence/hypoplasia of thumb" />
      </concept>
      <concept>
        <code value="ORPHA:295" />
        <display value="Fetal parvovirus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2950" />
        <display value="Triphalangeal thumb-polysyndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:295000" />
        <display value="Constriction rings syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:295002" />
        <display value="Hyperphalangy" />
      </concept>
      <concept>
        <code value="ORPHA:295004" />
        <display value="Central polydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:295012" />
        <display value="Syndactyly type 6" />
      </concept>
      <concept>
        <code value="ORPHA:295014" />
        <display value="Familial isolated clinodactyly of fingers" />
      </concept>
      <concept>
        <code value="ORPHA:295016" />
        <display value="Camptodactyly of fingers" />
      </concept>
      <concept>
        <code value="ORPHA:295018" />
        <display value="Congenital pseudoarthrosis of the tibia" />
      </concept>
      <concept>
        <code value="ORPHA:295020" />
        <display value="Congenital pseudoarthrosis of the femur" />
      </concept>
      <concept>
        <code value="ORPHA:295022" />
        <display value="Congenital pseudoarthrosis of the fibula" />
      </concept>
      <concept>
        <code value="ORPHA:295024" />
        <display value="Congenital pseudoarthrosis of the radius" />
      </concept>
      <concept>
        <code value="ORPHA:295026" />
        <display value="Congenital pseudoarthrosis of the ulna" />
      </concept>
      <concept>
        <code value="ORPHA:295028" />
        <display value="Tibio-fibular synostosis" />
      </concept>
      <concept>
        <code value="ORPHA:295030" />
        <display value="Congenital shoulder dislocation" />
      </concept>
      <concept>
        <code value="ORPHA:295032" />
        <display value="Isolated congenital radial head dislocation" />
      </concept>
      <concept>
        <code value="ORPHA:295034" />
        <display value="Congenital knee dislocation" />
      </concept>
      <concept>
        <code value="ORPHA:295036" />
        <display value="Congenital patella dislocation" />
      </concept>
      <concept>
        <code value="ORPHA:295044" />
        <display value="Macrodactyly of fingers" />
      </concept>
      <concept>
        <code value="ORPHA:295047" />
        <display value="Macrodactyly of toes" />
      </concept>
      <concept>
        <code value="ORPHA:295049" />
        <display value="Upper limb hypertrophy" />
      </concept>
      <concept>
        <code value="ORPHA:295051" />
        <display value="Lower limb hypertrophy" />
      </concept>
      <concept>
        <code value="ORPHA:2951" />
        <display value="Absent thumb-short stature-immunodeficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:295140" />
        <display value="Hyperphalangy, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295142" />
        <display value="Hyperphalangy, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295187" />
        <display value="Zygodactyly type 1" />
      </concept>
      <concept>
        <code value="ORPHA:295189" />
        <display value="Zygodactyly type 2" />
      </concept>
      <concept>
        <code value="ORPHA:295191" />
        <display value="Zygodactyly type 3" />
      </concept>
      <concept>
        <code value="ORPHA:295193" />
        <display value="Zygodactyly type 4" />
      </concept>
      <concept>
        <code value="ORPHA:295195" />
        <display value="Synpolydactyly type 1" />
      </concept>
      <concept>
        <code value="ORPHA:295197" />
        <display value="Synpolydactyly type 2" />
      </concept>
      <concept>
        <code value="ORPHA:295199" />
        <display value="Synpolydactyly type 3" />
      </concept>
      <concept>
        <code value="ORPHA:2952" />
        <display value="Adducted thumbs-arthrogryposis syndrome, Christian type" />
      </concept>
      <concept>
        <code value="ORPHA:295201" />
        <display value="Congenital vertical talus, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295203" />
        <display value="Congenital vertical talus, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295213" />
        <display value="Humero-ulnar synostosis, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295215" />
        <display value="Humero-ulnar synostosis, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295217" />
        <display value="Radio-ulnar synostosis, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295219" />
        <display value="Radio-ulnar synostosis, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295221" />
        <display value="Madelung deformity, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295223" />
        <display value="Madelung deformity, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295225" />
        <display value="Congenital elbow dislocation, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295227" />
        <display value="Congenital elbow dislocation, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295229" />
        <display value="Congenital genu recurvatum" />
      </concept>
      <concept>
        <code value="ORPHA:295232" />
        <display value="Congenital genu flexum" />
      </concept>
      <concept>
        <code value="ORPHA:295239" />
        <display value="Macrodactyly of fingers, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295241" />
        <display value="Macrodactyly of fingers, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295243" />
        <display value="Macrodactyly of toes, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:295245" />
        <display value="Macrodactyly of toes, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:2953" />
        <display value="Ehlers-Danlos syndrome, musculocontractural type" />
      </concept>
      <concept>
        <code value="ORPHA:2956" />
        <display value="Acrodysplasia scoliosis" />
      </concept>
      <concept>
        <code value="ORPHA:2957" />
        <display value="Guttmacher syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2958" />
        <display value="X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2959" />
        <display value="Progeria-short stature-pigmented nevi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:296" />
        <display value="Enchondromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:2962" />
        <display value="De Barsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2963" />
        <display value="Progeroid syndrome, Petty type" />
      </concept>
      <concept>
        <code value="ORPHA:2964" />
        <display value="Autosomal dominant prognathism" />
      </concept>
      <concept>
        <code value="ORPHA:2965" />
        <display value="Prolactinoma" />
      </concept>
      <concept>
        <code value="ORPHA:2966" />
        <display value="Properdin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2967" />
        <display value="Transcobalamin I deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2968" />
        <display value="Leukocyte adhesion deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2969" />
        <display value="Proteus-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:297" />
        <display value="Tick-borne encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:2970" />
        <display value="Prune belly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2971" />
        <display value="Peroxisomal acyl-CoA oxidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:2972" />
        <display value="Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2973" />
        <display value="46,XX disorder of sex development-anorectal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2975" />
        <display value="46,XX disorder of sex development-skeletal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2976" />
        <display value="Pseudoleprechaunism syndrome, Patterson type" />
      </concept>
      <concept>
        <code value="ORPHA:2978" />
        <display value="Chronic intestinal pseudoobstruction" />
      </concept>
      <concept>
        <code value="ORPHA:298" />
        <display value="Mitochondrial neurogastrointestinal encephalomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:2980" />
        <display value="Acrootoocular syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2982" />
        <display value="46,XX disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:29822" />
        <display value="Spontaneous periodic hypothermia" />
      </concept>
      <concept>
        <code value="ORPHA:2983" />
        <display value="Disorder of sex development-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2985" />
        <display value="Pseudoprogeria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:298644" />
        <display value="Disorder of thiamine metabolism and transport" />
      </concept>
      <concept>
        <code value="ORPHA:2987" />
        <display value="Antecubital pterygium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2988" />
        <display value="Pterygium colli-intellectual disability-digital anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2990" />
        <display value="Autosomal recessive multiple pterygium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2994" />
        <display value="Short stature-craniofacial anomalies-genital hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2995" />
        <display value="Baraitser-Winter cerebrofrontofacial syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2997" />
        <display value="Ptosis-vocal cord paralysis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:2999" />
        <display value="Ptosis-strabismus-ectopic pupils syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:30" />
        <display value="Hereditary orotic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:300" />
        <display value="Bifunctional enzyme deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3000" />
        <display value="Familial male-limited precocious puberty" />
      </concept>
      <concept>
        <code value="ORPHA:300179" />
        <display value="Ehlers-Danlos syndrome, kyphoscoliotic and deafness type" />
      </concept>
      <concept>
        <code value="ORPHA:3002" />
        <display value="Immune thrombocytopenic purpura" />
      </concept>
      <concept>
        <code value="ORPHA:300284" />
        <display value="Connective tissue disorder due to lysyl hydroxylase-3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:300293" />
        <display value="Transient infantile hypertriglyceridemia and hepatosteatosis" />
      </concept>
      <concept>
        <code value="ORPHA:300298" />
        <display value="Severe congenital hypochromic anemia with ringed sideroblasts" />
      </concept>
      <concept>
        <code value="ORPHA:3003" />
        <display value="Pyknoachondrogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:300305" />
        <display value="11p15.4 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300313" />
        <display value="Congenital cataract-hearing loss-severe developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300319" />
        <display value="Charcot-Marie-Tooth disease type 2P" />
      </concept>
      <concept>
        <code value="ORPHA:300324" />
        <display value="Persistent polyclonal B-cell lymphocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:300333" />
        <display value="Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300345" />
        <display value="Autosomal systemic lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:300359" />
        <display value="PLCG2-associated antibody deficiency and immune dysregulation" />
      </concept>
      <concept>
        <code value="ORPHA:300373" />
        <display value="Familial infantile gigantism" />
      </concept>
      <concept>
        <code value="ORPHA:300382" />
        <display value="Progeroid and marfanoid aspect-lipodystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300385" />
        <display value="Pituitary carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:3004" />
        <display value="Mirror polydactyly-vertebral segmentation-limbs defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300493" />
        <display value="Sagliker syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300496" />
        <display value="Multiple congenital anomalies-hypotonia-seizures syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:3005" />
        <display value="Pyle disease" />
      </concept>
      <concept>
        <code value="ORPHA:300501" />
        <display value="Painful orbital and systemic neurofibromas-marfanoid habitus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300504" />
        <display value="Onychocytic matricoma" />
      </concept>
      <concept>
        <code value="ORPHA:300512" />
        <display value="Onychomatricoma" />
      </concept>
      <concept>
        <code value="ORPHA:300515" />
        <display value="Rare nail tumor" />
      </concept>
      <concept>
        <code value="ORPHA:300525" />
        <display value="Pseudohypoaldosteronism type 2D" />
      </concept>
      <concept>
        <code value="ORPHA:300530" />
        <display value="Pseudohypoaldosteronism type 2E" />
      </concept>
      <concept>
        <code value="ORPHA:300536" />
        <display value="DDOST-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:300547" />
        <display value="Autosomal recessive infantile hypercalcemia" />
      </concept>
      <concept>
        <code value="ORPHA:300552" />
        <display value="Follicular cholangitis and pancreatitis" />
      </concept>
      <concept>
        <code value="ORPHA:300557" />
        <display value="Carcinoma of the ampulla of Vater" />
      </concept>
      <concept>
        <code value="ORPHA:300564" />
        <display value="Combined pulmonary fibrosis-emphysema syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300570" />
        <display value="Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:300573" />
        <display value="Polymicrogyria due to TUBB2B mutation" />
      </concept>
      <concept>
        <code value="ORPHA:300576" />
        <display value="Oligodontia-cancer predisposition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:300579" />
        <display value="Staphylococcal toxemia" />
      </concept>
      <concept>
        <code value="ORPHA:3006" />
        <display value="Pyridoxine-dependent epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:300605" />
        <display value="Juvenile amyotrophic lateral sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:300751" />
        <display value="Familial dilated cardiomyopathy with conduction defect due to LMNA mutation" />
      </concept>
      <concept>
        <code value="ORPHA:3008" />
        <display value="Pyruvate carboxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:300842" />
        <display value="Indolent B-cell non-Hodgkin lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:300846" />
        <display value="Aggressive B-cell non-Hodgkin lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:300849" />
        <display value="Diffuse large B-cell lymphoma of the central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:300857" />
        <display value="T-cell/histiocyte rich large B cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:300865" />
        <display value="Primary cutaneous anaplastic large cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:300869" />
        <display value="Splenic diffuse red pulp small B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:300878" />
        <display value="Hairy cell leukemia variant" />
      </concept>
      <concept>
        <code value="ORPHA:300888" />
        <display value="Diffuse large B-cell lymphoma with chronic inflammation" />
      </concept>
      <concept>
        <code value="ORPHA:300895" />
        <display value="ALK-positive anaplastic large cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:300903" />
        <display value="ALK-negative anaplastic large cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:300912" />
        <display value="Marginal zone lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:301" />
        <display value="Ependymal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:3010" />
        <display value="Qazi-Markouizos syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3011" />
        <display value="Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3015" />
        <display value="Radio-renal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3016" />
        <display value="Absent radius-anogenital anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3018" />
        <display value="Retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3019" />
        <display value="Ramon syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:302" />
        <display value="Epidermodysplasia verruciformis" />
      </concept>
      <concept>
        <code value="ORPHA:3020" />
        <display value="Ramsay Hunt syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3021" />
        <display value="RAPADILINO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3023" />
        <display value="External auditory canal atresia-vertical talus-hypertelorism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3026" />
        <display value="Radial ray hypoplasia-choanal atresia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3027" />
        <display value="Caudal regression sequence" />
      </concept>
      <concept>
        <code value="ORPHA:303" />
        <display value="Dystrophic epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:3032" />
        <display value="NPHP3-related Meckel-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3033" />
        <display value="Renal tubular dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:3034" />
        <display value="Delayed membranous cranial ossification" />
      </concept>
      <concept>
        <code value="ORPHA:3035" />
        <display value="Growth delay-hydrocephaly-lung hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3038" />
        <display value="Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:30391" />
        <display value="Isolated biliary atresia" />
      </concept>
      <concept>
        <code value="ORPHA:304" />
        <display value="Epidermolysis bullosa simplex" />
      </concept>
      <concept>
        <code value="ORPHA:304055" />
        <display value="Pituitary tumor" />
      </concept>
      <concept>
        <code value="ORPHA:3041" />
        <display value="Intellectual disability-balding-patella luxation-acromicria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3042" />
        <display value="Intellectual disability-cataracts-calcified pinnae-myopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3044" />
        <display value="Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3047" />
        <display value="Blepharophimosis-intellectual disability syndrome, SBBYS type" />
      </concept>
      <concept>
        <code value="ORPHA:305" />
        <display value="Junctional epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:3051" />
        <display value="Intellectual disability-sparse hair-brachydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3052" />
        <display value="X-linked intellectual disability-seizures-psoriasis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3055" />
        <display value="X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3056" />
        <display value="X-linked intellectual disability, Brooks type" />
      </concept>
      <concept>
        <code value="ORPHA:3057" />
        <display value="Monoamine oxidase A deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:306" />
        <display value="Benign familial infantile epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:3063" />
        <display value="X-linked intellectual disability, Snyder type" />
      </concept>
      <concept>
        <code value="ORPHA:306431" />
        <display value="Acquired adult-onset immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:306436" />
        <display value="Congenital sucrase-isomaltase deficiency with starch intolerance" />
      </concept>
      <concept>
        <code value="ORPHA:306446" />
        <display value="Congenital sucrase-isomaltase deficiency with minimal starch tolerance" />
      </concept>
      <concept>
        <code value="ORPHA:306462" />
        <display value="Congenital sucrase-isomaltase deficiency without starch intolerance" />
      </concept>
      <concept>
        <code value="ORPHA:306474" />
        <display value="Congenital sucrase-isomaltase deficiency with starch and lactose intolerance" />
      </concept>
      <concept>
        <code value="ORPHA:306486" />
        <display value="Congenital sucrase-isomaltase deficiency without sucrose intolerance" />
      </concept>
      <concept>
        <code value="ORPHA:306498" />
        <display value="PTEN hamartoma tumor syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306504" />
        <display value="Junctional epidermolysis bullosa with respiratory and renal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:306507" />
        <display value="LAMB2-related infantile-onset nephrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306511" />
        <display value="Autosomal recessive spastic paraplegia type 48" />
      </concept>
      <concept>
        <code value="ORPHA:306516" />
        <display value="Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis" />
      </concept>
      <concept>
        <code value="ORPHA:306519" />
        <display value="Familial primary hypomagnesemia with hypocalcuria" />
      </concept>
      <concept>
        <code value="ORPHA:306522" />
        <display value="Familial primary hypomagnesemia with normocalcuria" />
      </concept>
      <concept>
        <code value="ORPHA:306527" />
        <display value="Isolated hereditary congenital facial paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:306530" />
        <display value="Congenital hereditary facial paralysis-variable hearing loss syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306539" />
        <display value="Hereditary acrokeratotic poikiloderma of Kindler-Weary" />
      </concept>
      <concept>
        <code value="ORPHA:306542" />
        <display value="Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306547" />
        <display value="Porencephaly-microcephaly-bilateral congenital cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306550" />
        <display value="FADD-related immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:306553" />
        <display value="Myospherulosis" />
      </concept>
      <concept>
        <code value="ORPHA:306558" />
        <display value="Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306577" />
        <display value="Sodium channelopathy-related small fiber neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:306588" />
        <display value="Autosomal dominant Opitz G/BBB syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306597" />
        <display value="X-linked Opitz G/BBB syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306617" />
        <display value="X-linked complicated spastic paraplegia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:306633" />
        <display value="Rare tumor of gallbladder and extrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:306636" />
        <display value="Rare tumor of liver and intrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:306640" />
        <display value="Rare intoxication due to medical products" />
      </concept>
      <concept>
        <code value="ORPHA:306648" />
        <display value="Non-infectious anterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:306658" />
        <display value="Familial normophosphatemic tumoral calcinosis" />
      </concept>
      <concept>
        <code value="ORPHA:306661" />
        <display value="Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306666" />
        <display value="Rare parkinsonian syndrome due to neurodegenerative disease" />
      </concept>
      <concept>
        <code value="ORPHA:306669" />
        <display value="Hemiparkinsonism-hemiatrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306674" />
        <display value="Kufor-Rakeb syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306679" />
        <display value="Rare parkinsonian syndrome due to intoxication" />
      </concept>
      <concept>
        <code value="ORPHA:306682" />
        <display value="Manganese poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:306686" />
        <display value="Carbon monoxide-induced parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:306692" />
        <display value="Cyanide-induced parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:306695" />
        <display value="Miscellaneous movement disorder due to neurodegenerative disease" />
      </concept>
      <concept>
        <code value="ORPHA:306708" />
        <display value="Frontotemporal neurodegeneration with movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:306712" />
        <display value="Rare tremor disorder" />
      </concept>
      <concept>
        <code value="ORPHA:306715" />
        <display value="Rare choreic movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:306719" />
        <display value="Neurodegenerative disease with chorea" />
      </concept>
      <concept>
        <code value="ORPHA:306727" />
        <display value="Postinfectious autoimmune disease with chorea" />
      </concept>
      <concept>
        <code value="ORPHA:306731" />
        <display value="Sydenham chorea" />
      </concept>
      <concept>
        <code value="ORPHA:306734" />
        <display value="Primary dystonia, DYT21 type" />
      </concept>
      <concept>
        <code value="ORPHA:306741" />
        <display value="Hemidystonia-hemiatrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:306747" />
        <display value="Rare myoclonus" />
      </concept>
      <concept>
        <code value="ORPHA:306750" />
        <display value="Primary myoclonus" />
      </concept>
      <concept>
        <code value="ORPHA:306753" />
        <display value="Rare disease with myoclonus as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:306756" />
        <display value="Epilepsy and/or ataxia with myoclonus as major feature" />
      </concept>
      <concept>
        <code value="ORPHA:306759" />
        <display value="Non progressive epilepsy and/or ataxia with myoclonus as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:306765" />
        <display value="Motor stereotypies" />
      </concept>
      <concept>
        <code value="ORPHA:306768" />
        <display value="Rare paroxysmal movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:306773" />
        <display value="Hyperekplexia" />
      </concept>
      <concept>
        <code value="ORPHA:306776" />
        <display value="Sporadic hyperekplexia" />
      </concept>
      <concept>
        <code value="ORPHA:3068" />
        <display value="Intellectual disability-myopathy-short stature-endocrine defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:307" />
        <display value="Juvenile myoclonic epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:307052" />
        <display value="Rare genetic parkinsonian disorder" />
      </concept>
      <concept>
        <code value="ORPHA:307055" />
        <display value="Rare parkinsonian syndrome due to genetic neurodegenerative disease" />
      </concept>
      <concept>
        <code value="ORPHA:307058" />
        <display value="Miscellaneous movement disorder due to genetic neurodegenerative disease" />
      </concept>
      <concept>
        <code value="ORPHA:307061" />
        <display value="Rare genetic tremor disorder" />
      </concept>
      <concept>
        <code value="ORPHA:307064" />
        <display value="Rare genetic myoclonus" />
      </concept>
      <concept>
        <code value="ORPHA:307067" />
        <display value="Rare genetic disease with myoclonus as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:3071" />
        <display value="Costello syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:307141" />
        <display value="Diffuse palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:307148" />
        <display value="Isolated diffuse palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:3074" />
        <display value="Intellectual disability-short stature-hypertelorism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3077" />
        <display value="X-linked intellectual disability-psychosis-macroorchidism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:307711" />
        <display value="Disease with diffuse palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:307766" />
        <display value="Curly hair-acral keratoderma-caries syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:307773" />
        <display value="Autosomal dominant diffuse mutilating palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:3078" />
        <display value="Severe X-linked intellectual disability, Gustavson type" />
      </concept>
      <concept>
        <code value="ORPHA:307804" />
        <display value="Autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:307837" />
        <display value="Focal palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:307846" />
        <display value="Isolated focal palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:307871" />
        <display value="Disease with focal palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:3079" />
        <display value="Intellectual disability, Buenos-Aires type" />
      </concept>
      <concept>
        <code value="ORPHA:307936" />
        <display value="Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:307967" />
        <display value="Punctate palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:307995" />
        <display value="Marginal papular palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:308" />
        <display value="Unverricht-Lundborg disease" />
      </concept>
      <concept>
        <code value="ORPHA:3080" />
        <display value="Intellectual disability, Wolff type" />
      </concept>
      <concept>
        <code value="ORPHA:308013" />
        <display value="Focal acral hyperkeratosis" />
      </concept>
      <concept>
        <code value="ORPHA:308023" />
        <display value="Disease with punctate palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:308031" />
        <display value="Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:308041" />
        <display value="Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:308166" />
        <display value="Erythrokeratoderma variabilis progressiva" />
      </concept>
      <concept>
        <code value="ORPHA:3082" />
        <display value="Intellectual disability-polydactyly-uncombable hair syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:308380" />
        <display value="Methylcobalamin deficiency type cblDv1" />
      </concept>
      <concept>
        <code value="ORPHA:308386" />
        <display value="Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A" />
      </concept>
      <concept>
        <code value="ORPHA:308393" />
        <display value="Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B" />
      </concept>
      <concept>
        <code value="ORPHA:308400" />
        <display value="Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C" />
      </concept>
      <concept>
        <code value="ORPHA:308407" />
        <display value="Disorder of beta and omega amino acid metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:308410" />
        <display value="Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:308425" />
        <display value="Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:308442" />
        <display value="Vitamin B12-responsive methylmalonic acidemia, type cblDv2" />
      </concept>
      <concept>
        <code value="ORPHA:308448" />
        <display value="Aminoacylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:308451" />
        <display value="Disorder of neutral amino acid transport" />
      </concept>
      <concept>
        <code value="ORPHA:308459" />
        <display value="Disorder of glycolysis" />
      </concept>
      <concept>
        <code value="ORPHA:308463" />
        <display value="Disorder of fructose metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:308467" />
        <display value="Disorder of galactose metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:308473" />
        <display value="Erythrocyte galactose epimerase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:308487" />
        <display value="Generalized galactose epimerase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3085" />
        <display value="Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:308520" />
        <display value="Glycogen storage disease due to glycogen synthase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:308552" />
        <display value="Glycogen storage disease due to acid maltase deficiency, infantile onset" />
      </concept>
      <concept>
        <code value="ORPHA:3086" />
        <display value="Autosomal dominant vitreoretinochoroidopathy" />
      </concept>
      <concept>
        <code value="ORPHA:308621" />
        <display value="Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form" />
      </concept>
      <concept>
        <code value="ORPHA:308638" />
        <display value="Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form" />
      </concept>
      <concept>
        <code value="ORPHA:308655" />
        <display value="Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form" />
      </concept>
      <concept>
        <code value="ORPHA:308670" />
        <display value="Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form" />
      </concept>
      <concept>
        <code value="ORPHA:308684" />
        <display value="Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form" />
      </concept>
      <concept>
        <code value="ORPHA:308698" />
        <display value="Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form" />
      </concept>
      <concept>
        <code value="ORPHA:3087" />
        <display value="Retinohepatoendocrinologic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:308712" />
        <display value="Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form" />
      </concept>
      <concept>
        <code value="ORPHA:3088" />
        <display value="Revesz syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:308993" />
        <display value="Glycerol kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:308998" />
        <display value="Disorder of glyoxylate metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:309" />
        <display value="Familial partial epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:3090" />
        <display value="Congenital pulmonary venous return anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:309001" />
        <display value="Disorder of carbohydrate absorption and transport" />
      </concept>
      <concept>
        <code value="ORPHA:309005" />
        <display value="Disorder of lipid metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:309015" />
        <display value="Familial lipoprotein lipase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:309020" />
        <display value="Familial apolipoprotein C-II deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:309025" />
        <display value="Mevalonate kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:309028" />
        <display value="Disorder of lipid absorption and transport" />
      </concept>
      <concept>
        <code value="ORPHA:309031" />
        <display value="Pancreatic triacylglycerol lipase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3091" />
        <display value="Congenital systemic veins anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:309108" />
        <display value="Pancreatic colipase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:309111" />
        <display value="Combined pancreatic lipase-colipase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:309115" />
        <display value="Disorder of fatty acid oxidation and ketogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:309120" />
        <display value="Acyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:309127" />
        <display value="3-hydroxyacyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:309130" />
        <display value="Disorder of carnitine cycle and carnitine transport" />
      </concept>
      <concept>
        <code value="ORPHA:309133" />
        <display value="Metabolic disease due to other fatty acid oxidation disorder" />
      </concept>
      <concept>
        <code value="ORPHA:309136" />
        <display value="Mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes" />
      </concept>
      <concept>
        <code value="ORPHA:309144" />
        <display value="Gangliosidosis" />
      </concept>
      <concept>
        <code value="ORPHA:309147" />
        <display value="Hyper-beta-alaninemia" />
      </concept>
      <concept>
        <code value="ORPHA:309152" />
        <display value="GM2 gangliosidosis" />
      </concept>
      <concept>
        <code value="ORPHA:309155" />
        <display value="Sandhoff disease, infantile form" />
      </concept>
      <concept>
        <code value="ORPHA:309162" />
        <display value="Sandhoff disease, juvenile form" />
      </concept>
      <concept>
        <code value="ORPHA:309169" />
        <display value="Sandhoff disease, adult form" />
      </concept>
      <concept>
        <code value="ORPHA:309178" />
        <display value="Tay-Sachs disease, B variant, infantile form" />
      </concept>
      <concept>
        <code value="ORPHA:309185" />
        <display value="Tay-Sachs disease, B variant, juvenile form" />
      </concept>
      <concept>
        <code value="ORPHA:309192" />
        <display value="Tay-Sachs disease, B variant, adult form" />
      </concept>
      <concept>
        <code value="ORPHA:3092" />
        <display value="Fixed subaortic stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:309239" />
        <display value="Tay-Sachs disease, B1 variant" />
      </concept>
      <concept>
        <code value="ORPHA:30924" />
        <display value="Primary hypomagnesemia with secondary hypocalcemia" />
      </concept>
      <concept>
        <code value="ORPHA:309246" />
        <display value="GM2 gangliosidosis, AB variant" />
      </concept>
      <concept>
        <code value="ORPHA:30925" />
        <display value="Hereditary central diabetes insipidus" />
      </concept>
      <concept>
        <code value="ORPHA:309252" />
        <display value="Atypical Gaucher disease due to saposin C deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:309256" />
        <display value="Metachromatic leukodystrophy, late infantile form" />
      </concept>
      <concept>
        <code value="ORPHA:309263" />
        <display value="Metachromatic leukodystrophy, juvenile form" />
      </concept>
      <concept>
        <code value="ORPHA:309271" />
        <display value="Metachromatic leukodystrophy, adult form" />
      </concept>
      <concept>
        <code value="ORPHA:309279" />
        <display value="Glycoproteinosis" />
      </concept>
      <concept>
        <code value="ORPHA:309282" />
        <display value="Alpha-mannosidosis, infantile form" />
      </concept>
      <concept>
        <code value="ORPHA:309288" />
        <display value="Alpha-mannosidosis, adult form" />
      </concept>
      <concept>
        <code value="ORPHA:309294" />
        <display value="Sialidosis" />
      </concept>
      <concept>
        <code value="ORPHA:309297" />
        <display value="Mucopolysaccharidosis type 4A" />
      </concept>
      <concept>
        <code value="ORPHA:3093" />
        <display value="Congenital aortic valve stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:309310" />
        <display value="Mucopolysaccharidosis type 4B" />
      </concept>
      <concept>
        <code value="ORPHA:309319" />
        <display value="Disorder of sialic acid metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:309324" />
        <display value="Free sialic acid storage disease, infantile form" />
      </concept>
      <concept>
        <code value="ORPHA:309331" />
        <display value="Intermediate severe Salla disease" />
      </concept>
      <concept>
        <code value="ORPHA:309334" />
        <display value="Salla disease" />
      </concept>
      <concept>
        <code value="ORPHA:309337" />
        <display value="Lysosomal glycogen storage disease" />
      </concept>
      <concept>
        <code value="ORPHA:309340" />
        <display value="Disorder of lysosomal-related organelles" />
      </concept>
      <concept>
        <code value="ORPHA:309347" />
        <display value="Disorder of protein N-glycosylation" />
      </concept>
      <concept>
        <code value="ORPHA:309447" />
        <display value="Disorder of protein O-glycosylation" />
      </concept>
      <concept>
        <code value="ORPHA:309450" />
        <display value="Disorder of O-xylosylglycan synthesis" />
      </concept>
      <concept>
        <code value="ORPHA:309458" />
        <display value="Disorder of O-N-acetylgalactosaminylglycan synthesis" />
      </concept>
      <concept>
        <code value="ORPHA:309463" />
        <display value="Disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis" />
      </concept>
      <concept>
        <code value="ORPHA:309469" />
        <display value="Disorder of O-mannosylglycan synthesis" />
      </concept>
      <concept>
        <code value="ORPHA:3095" />
        <display value="Atypical Rett syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:309505" />
        <display value="Disorder of fucoglycosan synthesis" />
      </concept>
      <concept>
        <code value="ORPHA:309515" />
        <display value="Disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation" />
      </concept>
      <concept>
        <code value="ORPHA:309526" />
        <display value="Disorder of multiple glycosylation" />
      </concept>
      <concept>
        <code value="ORPHA:309568" />
        <display value="Defect in conserved oligomeric Golgi complex" />
      </concept>
      <concept>
        <code value="ORPHA:3096" />
        <display value="Reye syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3097" />
        <display value="Meacham syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:309778" />
        <display value="Defect in V-ATPase" />
      </concept>
      <concept>
        <code value="ORPHA:309789" />
        <display value="Rhizomelic chondrodysplasia punctata type 1" />
      </concept>
      <concept>
        <code value="ORPHA:309796" />
        <display value="Rhizomelic chondrodysplasia punctata type 2" />
      </concept>
      <concept>
        <code value="ORPHA:3098" />
        <display value="Rhizomelic syndrome, Urbach type" />
      </concept>
      <concept>
        <code value="ORPHA:309803" />
        <display value="Rhizomelic chondrodysplasia punctata type 3" />
      </concept>
      <concept>
        <code value="ORPHA:309810" />
        <display value="Disorder of peroxisomal alpha-, beta- and omega-oxidation" />
      </concept>
      <concept>
        <code value="ORPHA:309813" />
        <display value="Disorder of porphyrin and haem metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:309816" />
        <display value="Disorder of bilirubin metabolism and excretion" />
      </concept>
      <concept>
        <code value="ORPHA:309819" />
        <display value="Disorder of pterin metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:309824" />
        <display value="Disorder of metabolite absorption and transport" />
      </concept>
      <concept>
        <code value="ORPHA:309827" />
        <display value="Disorder of vitamin and non-protein cofactor absorption and transport" />
      </concept>
      <concept>
        <code value="ORPHA:309830" />
        <display value="Disorder of catecholamine synthesis" />
      </concept>
      <concept>
        <code value="ORPHA:309833" />
        <display value="Disorder of other vitamins and cofactors metabolism and transport" />
      </concept>
      <concept>
        <code value="ORPHA:309836" />
        <display value="Disorder of mineral absorption and transport" />
      </concept>
      <concept>
        <code value="ORPHA:309839" />
        <display value="Disorder of copper metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:309842" />
        <display value="Disorder of iron metabolism and transport" />
      </concept>
      <concept>
        <code value="ORPHA:309845" />
        <display value="Disorder of zinc metabolism and transport" />
      </concept>
      <concept>
        <code value="ORPHA:309848" />
        <display value="Disorder of magnesium transport" />
      </concept>
      <concept>
        <code value="ORPHA:309851" />
        <display value="Disorder of manganese transport" />
      </concept>
      <concept>
        <code value="ORPHA:309854" />
        <display value="Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3099" />
        <display value="Rheumatic fever" />
      </concept>
      <concept>
        <code value="ORPHA:31" />
        <display value="Oxoglutaricaciduria" />
      </concept>
      <concept>
        <code value="ORPHA:310" />
        <display value="Reflex epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:310050" />
        <display value="Acquired immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3101" />
        <display value="Richieri Costa-da Silva syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3102" />
        <display value="Richieri Costa-Pereira syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3103" />
        <display value="Roberts syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3104" />
        <display value="Robin sequence-oligodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:31043" />
        <display value="Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement" />
      </concept>
      <concept>
        <code value="ORPHA:3105" />
        <display value="Robinow-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3107" />
        <display value="Autosomal dominant Robinow syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3109" />
        <display value="Mayer-Rokitansky-Kuster-Hauser syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3110" />
        <display value="Rombo syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3111" />
        <display value="Rotor syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:31112" />
        <display value="Dermatofibrosarcoma protuberans" />
      </concept>
      <concept>
        <code value="ORPHA:31142" />
        <display value="Oral erosive lichen" />
      </concept>
      <concept>
        <code value="ORPHA:3115" />
        <display value="Roussy-Levy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:31150" />
        <display value="Tangier disease" />
      </concept>
      <concept>
        <code value="ORPHA:31153" />
        <display value="Hypoalphalipoproteinemia" />
      </concept>
      <concept>
        <code value="ORPHA:31154" />
        <display value="Hypobetalipoproteinemia" />
      </concept>
      <concept>
        <code value="ORPHA:312" />
        <display value="Autosomal dominant epidermolytic ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:31202" />
        <display value="Melioidosis" />
      </concept>
      <concept>
        <code value="ORPHA:31204" />
        <display value="Nocardiosis" />
      </concept>
      <concept>
        <code value="ORPHA:31205" />
        <display value="Rat-bite fever" />
      </concept>
      <concept>
        <code value="ORPHA:3121" />
        <display value="Ruvalcaba syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3124" />
        <display value="Saccharopinuria" />
      </concept>
      <concept>
        <code value="ORPHA:3129" />
        <display value="Sarcosinemia" />
      </concept>
      <concept>
        <code value="ORPHA:313" />
        <display value="Lamellar ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:3130" />
        <display value="Satoyoshi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3132" />
        <display value="Say-Barber-Miller syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3133" />
        <display value="Say-Field-Coldwell syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3134" />
        <display value="SCARF syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3135" />
        <display value="Familial Scheuermann disease" />
      </concept>
      <concept>
        <code value="ORPHA:3137" />
        <display value="Alpha-N-acetylgalactosaminidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:313772" />
        <display value="Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:313781" />
        <display value="20p13 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:313795" />
        <display value="Jawad syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3138" />
        <display value="Ulnar-mammary syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:313800" />
        <display value="Optic nerve edema-splenomegaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:313808" />
        <display value="Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia" />
      </concept>
      <concept>
        <code value="ORPHA:313838" />
        <display value="Coats plus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:313846" />
        <display value="Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:313850" />
        <display value="Infantile cerebellar-retinal degeneration" />
      </concept>
      <concept>
        <code value="ORPHA:313855" />
        <display value="FGFR2-related bent bone dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:313884" />
        <display value="12p12.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:313892" />
        <display value="Developmental and speech delay due to SOX5 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:313906" />
        <display value="Congenital pancreatic cyst" />
      </concept>
      <concept>
        <code value="ORPHA:313920" />
        <display value="Epstein-Barr virus-associated gastric carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:313936" />
        <display value="PENS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:313947" />
        <display value="2q23.1 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314" />
        <display value="Erythroderma desquamativum" />
      </concept>
      <concept>
        <code value="ORPHA:314002" />
        <display value="Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314017" />
        <display value="Idiopathic linear interstitial keratitis" />
      </concept>
      <concept>
        <code value="ORPHA:314022" />
        <display value="Gastric adenocarcinoma and proximal polyposis of the stomach" />
      </concept>
      <concept>
        <code value="ORPHA:314029" />
        <display value="High bone mass osteogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:314034" />
        <display value="7p22.1 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314041" />
        <display value="Marfanoid habitus-inguinal hernia-advanced bone age syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314051" />
        <display value="Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3143" />
        <display value="Autoimmune polyendocrinopathy type 2" />
      </concept>
      <concept>
        <code value="ORPHA:314373" />
        <display value="Chronic diarrhea due to guanylate cyclase 2C overactivity" />
      </concept>
      <concept>
        <code value="ORPHA:314376" />
        <display value="Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:314381" />
        <display value="Hereditary sensory and autonomic neuropathy type 6" />
      </concept>
      <concept>
        <code value="ORPHA:314389" />
        <display value="Xq12-q13.3 duplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314394" />
        <display value="Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314399" />
        <display value="Autosomal dominant aplasia and myelodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:3144" />
        <display value="Schneckenbecken dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:314404" />
        <display value="Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314419" />
        <display value="Ameloblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:314422" />
        <display value="Ameloblastic carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:314425" />
        <display value="Rare odontogenic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:314432" />
        <display value="Spigelian hernia-cryptorchidism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314451" />
        <display value="Meigs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314459" />
        <display value="Pseudo-Meigs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314466" />
        <display value="Atypical Meigs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314473" />
        <display value="Ovarian fibroma" />
      </concept>
      <concept>
        <code value="ORPHA:314478" />
        <display value="Ovarian fibrothecoma" />
      </concept>
      <concept>
        <code value="ORPHA:314485" />
        <display value="Young adult-onset distal hereditary motor neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:3145" />
        <display value="Nephrogenic diabetes insipidus-intracranial calcification syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314555" />
        <display value="Craniofacial dysplasia-osteopenia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314566" />
        <display value="Primary progressive apraxia of speech" />
      </concept>
      <concept>
        <code value="ORPHA:314572" />
        <display value="Autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314575" />
        <display value="Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314585" />
        <display value="15q overgrowth syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314588" />
        <display value="Distal tetrasomy 15q" />
      </concept>
      <concept>
        <code value="ORPHA:314597" />
        <display value="Chudley-McCullough syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314603" />
        <display value="Autosomal recessive spastic ataxia with leukoencephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:314613" />
        <display value="Growing teratoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314621" />
        <display value="Duplication of the pituitary gland" />
      </concept>
      <concept>
        <code value="ORPHA:314629" />
        <display value="CLN11 disease" />
      </concept>
      <concept>
        <code value="ORPHA:314632" />
        <display value="ATP13A2-related juvenile neuronal ceroid lipofuscinosis" />
      </concept>
      <concept>
        <code value="ORPHA:314637" />
        <display value="Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:314647" />
        <display value="Non-progressive cerebellar ataxia with intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:314652" />
        <display value="Variant ABeta2M amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:314655" />
        <display value="Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:314662" />
        <display value="Segmental progressive overgrowth syndrome with fibroadipose hyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:314667" />
        <display value="TMEM165-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:314679" />
        <display value="Cerebrofacioarticular syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314684" />
        <display value="Primary bone lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:314689" />
        <display value="Combined immunodeficiency due to STK4 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:314697" />
        <display value="Acquired porencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:314701" />
        <display value="Primary systemic amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:314709" />
        <display value="Primary localized amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:314718" />
        <display value="Lethal arteriopathy syndrome due to fibulin-4 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:314721" />
        <display value="Atypical dentin dysplasia due to SMOC2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:314749" />
        <display value="Rare disease with Cushing syndrome as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:314753" />
        <display value="Functioning pituitary adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:314759" />
        <display value="Mixed functioning pituitary adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:314769" />
        <display value="Somatomammotropinoma" />
      </concept>
      <concept>
        <code value="ORPHA:314777" />
        <display value="Familial isolated pituitary adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:314786" />
        <display value="Silent pituitary adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:314790" />
        <display value="Null pituitary adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:314795" />
        <display value="SHOX-related short stature" />
      </concept>
      <concept>
        <code value="ORPHA:3148" />
        <display value="Malignant peripheral nerve sheath tumor" />
      </concept>
      <concept>
        <code value="ORPHA:314802" />
        <display value="Short stature due to partial GHR deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:314811" />
        <display value="Short stature due to GHSR deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:314822" />
        <display value="Primary renal tubular acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:314889" />
        <display value="Autosomal dominant proximal renal tubular acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:314911" />
        <display value="Severe Canavan disease" />
      </concept>
      <concept>
        <code value="ORPHA:314918" />
        <display value="Mild Canavan disease" />
      </concept>
      <concept>
        <code value="ORPHA:314928" />
        <display value="Normal pressure hydrocephalus" />
      </concept>
      <concept>
        <code value="ORPHA:314946" />
        <display value="Mycobacterium xenopi infection" />
      </concept>
      <concept>
        <code value="ORPHA:314950" />
        <display value="Primary hypereosinophilic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314962" />
        <display value="Secondary hypereosinophilic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314970" />
        <display value="Lymphocytic hypereosinophilic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:314978" />
        <display value="X-linked non progressive cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:314993" />
        <display value="Cataract-congenital heart disease-neural tube defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:315" />
        <display value="Erythrokeratoderma en cocardes" />
      </concept>
      <concept>
        <code value="ORPHA:3151" />
        <display value="Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3152" />
        <display value="Sclerosteosis" />
      </concept>
      <concept>
        <code value="ORPHA:315306" />
        <display value="Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form" />
      </concept>
      <concept>
        <code value="ORPHA:315311" />
        <display value="Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form" />
      </concept>
      <concept>
        <code value="ORPHA:315350" />
        <display value="Autoimmune disease with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:3156" />
        <display value="Senior-Loken syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3157" />
        <display value="Septo-optic dysplasia spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:316" />
        <display value="Progressive symmetric erythrokeratodermia" />
      </concept>
      <concept>
        <code value="ORPHA:3161" />
        <display value="Congenital pulmonary sequestration" />
      </concept>
      <concept>
        <code value="ORPHA:3162" />
        <display value="Sezary syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:316226" />
        <display value="Spastic ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:316235" />
        <display value="Autosomal dominant spastic ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:316240" />
        <display value="Autosomal recessive spastic ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:316244" />
        <display value="Partial deletion of the short arm of chromosome 12" />
      </concept>
      <concept>
        <code value="ORPHA:3163" />
        <display value="SHORT syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3164" />
        <display value="Omphalocele syndrome, Shprintzen-Goldberg type" />
      </concept>
      <concept>
        <code value="ORPHA:3165" />
        <display value="Eosinophilic fasciitis" />
      </concept>
      <concept>
        <code value="ORPHA:3166" />
        <display value="Sialuria" />
      </concept>
      <concept>
        <code value="ORPHA:3167" />
        <display value="Siegler-Brewer-Carey syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3168" />
        <display value="Sillence syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3169" />
        <display value="Sirenomelia" />
      </concept>
      <concept>
        <code value="ORPHA:317" />
        <display value="Erythrokeratodermia variabilis" />
      </concept>
      <concept>
        <code value="ORPHA:31709" />
        <display value="Infantile convulsions and choreoathetosis" />
      </concept>
      <concept>
        <code value="ORPHA:3172" />
        <display value="Eyebrow duplication-syndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3173" />
        <display value="Infantile spasms-broad thumbs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:31740" />
        <display value="Hypersensitivity pneumonitis" />
      </concept>
      <concept>
        <code value="ORPHA:317416" />
        <display value="T-B+ severe combined immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:317419" />
        <display value="T-B- severe combined immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:317425" />
        <display value="Severe combined immunodeficiency due to DNA-PKcs deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:317428" />
        <display value="Combined immunodeficiency due to ORAI1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:317430" />
        <display value="Combined immunodeficiency due to STIM1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:317473" />
        <display value="Pancytopenia due to IKZF1 mutations" />
      </concept>
      <concept>
        <code value="ORPHA:317476" />
        <display value="X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:3175" />
        <display value="X-linked spasticity-intellectual disability-epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3176" />
        <display value="Spina bifida-hypospadias syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3177" />
        <display value="Spinocerebellar degeneration-corneal dystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:318" />
        <display value="Acute erythroid leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:3180" />
        <display value="Spondylocamptodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3181" />
        <display value="Sprengel deformity" />
      </concept>
      <concept>
        <code value="ORPHA:31824" />
        <display value="Colchicine poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:31825" />
        <display value="Methanol poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:31826" />
        <display value="Ethylene glycol poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:31827" />
        <display value="Paraquat poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:31828" />
        <display value="Digitalis poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:31837" />
        <display value="Pulmonary venoocclusive disease" />
      </concept>
      <concept>
        <code value="ORPHA:3184" />
        <display value="Steatocystoma multiplex-natal teeth syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3186" />
        <display value="Holoprosencephaly-radial heart renal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3188" />
        <display value="Congenital pulmonary veins atresia or stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:3189" />
        <display value="Congenital pulmonary valve stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:319" />
        <display value="Ewing sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:3190" />
        <display value="Subpulmonary stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:3191" />
        <display value="Subaortic stenosis-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:319160" />
        <display value="Congenital myopathy with internal nuclei and atypical cores" />
      </concept>
      <concept>
        <code value="ORPHA:319171" />
        <display value="Distal 17p13.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:319182" />
        <display value="Wiedemann-Steiner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:319189" />
        <display value="Familial cortical myoclonus" />
      </concept>
      <concept>
        <code value="ORPHA:319192" />
        <display value="Diencephalic-mesencephalic junction dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:319195" />
        <display value="Chondroectodermal dysplasia with night blindness" />
      </concept>
      <concept>
        <code value="ORPHA:319199" />
        <display value="Autosomal recessive spastic paraplegia type 53" />
      </concept>
      <concept>
        <code value="ORPHA:3192" />
        <display value="Supravalvular pulmonary stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:319205" />
        <display value="Bilateral massive adrenal hemorrhage" />
      </concept>
      <concept>
        <code value="ORPHA:319213" />
        <display value="Lujo hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:319218" />
        <display value="Ebola hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:319223" />
        <display value="Argentine hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:319229" />
        <display value="Bolivian hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:319234" />
        <display value="Venezuelan hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:319239" />
        <display value="Brazilian hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:319244" />
        <display value="Chapare hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:319247" />
        <display value="Hantavirus pulmonary syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:319251" />
        <display value="Rift valley fever" />
      </concept>
      <concept>
        <code value="ORPHA:319254" />
        <display value="Kyasanur forest disease" />
      </concept>
      <concept>
        <code value="ORPHA:319266" />
        <display value="Omsk hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:319276" />
        <display value="Clear cell renal carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:319287" />
        <display value="Multilocular cystic renal neoplasm of low malignant potential" />
      </concept>
      <concept>
        <code value="ORPHA:319298" />
        <display value="Papillary renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:3193" />
        <display value="Supravalvular aortic stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:319303" />
        <display value="Chromophobe renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:319308" />
        <display value="MiT family translocation renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:319314" />
        <display value="Renal cell carcinoma associated with neuroblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:319319" />
        <display value="Renal medullary carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:319322" />
        <display value="Mucinous tubular and spindle cell renal carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:319325" />
        <display value="Tubulocystic renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:319328" />
        <display value="Inherited renal cancer-predisposing syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:319332" />
        <display value="Autosomal recessive myogenic arthrogryposis multiplex congenita" />
      </concept>
      <concept>
        <code value="ORPHA:319340" />
        <display value="Carney complex-trismus-pseudocamptodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3194" />
        <display value="Corneodermatoosseous syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:319462" />
        <display value="Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations" />
      </concept>
      <concept>
        <code value="ORPHA:319465" />
        <display value="Inherited acute myeloid leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:319480" />
        <display value="Acute myeloid leukemia with CEBPA somatic mutations" />
      </concept>
      <concept>
        <code value="ORPHA:319487" />
        <display value="Familial papillary or follicular thyroid carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:319494" />
        <display value="Familial nonmedullary thyroid carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:319504" />
        <display value="Combined oxidative phosphorylation defect type 8" />
      </concept>
      <concept>
        <code value="ORPHA:319509" />
        <display value="Combined oxidative phosphorylation defect type 9" />
      </concept>
      <concept>
        <code value="ORPHA:319514" />
        <display value="Combined oxidative phosphorylation defect type 13" />
      </concept>
      <concept>
        <code value="ORPHA:319519" />
        <display value="Combined oxidative phosphorylation defect type 14" />
      </concept>
      <concept>
        <code value="ORPHA:319524" />
        <display value="Combined oxidative phosphorylation defect type 15" />
      </concept>
      <concept>
        <code value="ORPHA:319535" />
        <display value="Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319539" />
        <display value="Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319543" />
        <display value="Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319547" />
        <display value="Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319552" />
        <display value="Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319558" />
        <display value="Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319563" />
        <display value="Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319569" />
        <display value="Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319574" />
        <display value="Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319581" />
        <display value="Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319589" />
        <display value="Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319595" />
        <display value="Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3196" />
        <display value="Steroid dehydrogenase deficiency-dental anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:319600" />
        <display value="Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319605" />
        <display value="X-linked mendelian susceptibility to mycobacterial diseases" />
      </concept>
      <concept>
        <code value="ORPHA:319612" />
        <display value="X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319623" />
        <display value="X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:319635" />
        <display value="Amyloidosis cutis dyschromia" />
      </concept>
      <concept>
        <code value="ORPHA:319640" />
        <display value="Retinal macular dystrophy type 2" />
      </concept>
      <concept>
        <code value="ORPHA:319646" />
        <display value="PGM1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:319651" />
        <display value="Constitutional megaloblastic anemia with severe neurologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:319667" />
        <display value="Primary lymphoma of the conjunctiva" />
      </concept>
      <concept>
        <code value="ORPHA:319671" />
        <display value="Microcephalic primordial dwarfism, Alazami type" />
      </concept>
      <concept>
        <code value="ORPHA:319675" />
        <display value="Microcephalic primordial dwarfism, Dauber type" />
      </concept>
      <concept>
        <code value="ORPHA:319678" />
        <display value="Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3197" />
        <display value="Hereditary hyperekplexia" />
      </concept>
      <concept>
        <code value="ORPHA:319719" />
        <display value="Autoinflammatory syndrome of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:3198" />
        <display value="Stiff person syndrome and related disorders" />
      </concept>
      <concept>
        <code value="ORPHA:3199" />
        <display value="Stimmler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:32" />
        <display value="Glutathione synthetase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:320" />
        <display value="Apparent mineralocorticoid excess" />
      </concept>
      <concept>
        <code value="ORPHA:3200" />
        <display value="Arthrogryposis-ectodermal dysplasia-other anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3201" />
        <display value="Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3202" />
        <display value="Dehydrated hereditary stomatocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:3203" />
        <display value="Overhydrated hereditary stomatocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:320317" />
        <display value="Cleft lip/palate-ectodermal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:320332" />
        <display value="X-linked pure spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:320335" />
        <display value="Pure or complex hereditary spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:320342" />
        <display value="Pure or complex autosomal dominant spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:320346" />
        <display value="Pure or complex autosomal recessive spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:320350" />
        <display value="Pure or complex X-linked spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:320355" />
        <display value="Autosomal dominant spastic paraplegia type 41" />
      </concept>
      <concept>
        <code value="ORPHA:320360" />
        <display value="MT-ATP6-related mitochondrial spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:320365" />
        <display value="Autosomal dominant spastic paraplegia type 36" />
      </concept>
      <concept>
        <code value="ORPHA:320370" />
        <display value="Autosomal recessive spastic paraplegia type 43" />
      </concept>
      <concept>
        <code value="ORPHA:320375" />
        <display value="Autosomal recessive spastic paraplegia type 55" />
      </concept>
      <concept>
        <code value="ORPHA:320380" />
        <display value="Autosomal recessive spastic paraplegia type 54" />
      </concept>
      <concept>
        <code value="ORPHA:320385" />
        <display value="Hereditary sensory and autonomic neuropathy due to TECPR2 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:320391" />
        <display value="Autosomal recessive spastic paraplegia type 46" />
      </concept>
      <concept>
        <code value="ORPHA:320396" />
        <display value="Autosomal recessive spastic paraplegia type 45" />
      </concept>
      <concept>
        <code value="ORPHA:3204" />
        <display value="Stormorken-Sjaastad-Langslet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:320401" />
        <display value="Autosomal recessive spastic paraplegia type 44" />
      </concept>
      <concept>
        <code value="ORPHA:320406" />
        <display value="Spastic paraplegia-optic atrophy-neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:320411" />
        <display value="Autosomal recessive spastic paraplegia type 56" />
      </concept>
      <concept>
        <code value="ORPHA:3205" />
        <display value="Sturge-Weber syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3206" />
        <display value="Stuve-Wiedemann syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3207" />
        <display value="White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3208" />
        <display value="Isolated succinate-CoQ reductase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:321" />
        <display value="Multiple osteochondromas" />
      </concept>
      <concept>
        <code value="ORPHA:3210" />
        <display value="Summitt syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3214" />
        <display value="Deaf blind hypopigmentation syndrome, Yemenite type" />
      </concept>
      <concept>
        <code value="ORPHA:3216" />
        <display value="Conductive deafness-malformed external ear syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3217" />
        <display value="Deafness-small bowel diverticulosis-neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3218" />
        <display value="Deafness-epiphyseal dysplasia-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3219" />
        <display value="Fountain syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:322" />
        <display value="Exstrophy-epispadias complex" />
      </concept>
      <concept>
        <code value="ORPHA:3220" />
        <display value="Deafness-enamel hypoplasia-nail defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3221" />
        <display value="Generalized resistance to thyroid hormone" />
      </concept>
      <concept>
        <code value="ORPHA:322126" />
        <display value="Genetic tumor of hematopoietic and lymphoid tissues" />
      </concept>
      <concept>
        <code value="ORPHA:3222" />
        <display value="Phosphoribosylpyrophosphate synthetase superactivity" />
      </concept>
      <concept>
        <code value="ORPHA:3224" />
        <display value="Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3225" />
        <display value="Hearing loss-familial salivary gland insensitivity to aldosterone syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3226" />
        <display value="Deafness-lymphedema-leukemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3230" />
        <display value="Deafness-oligodontia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3231" />
        <display value="Deafness-onychodystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3232" />
        <display value="Deafness-ear malformation-facial palsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3233" />
        <display value="Cochleosaccular degeneration-cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3235" />
        <display value="Progressive deafness with stapes fixation" />
      </concept>
      <concept>
        <code value="ORPHA:3236" />
        <display value="Conductive deafness-ptosis-skeletal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3237" />
        <display value="Multiple synostoses syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3238" />
        <display value="Cardiospondylocarpofacial syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3239" />
        <display value="Deafness-vitiligo-achalasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324" />
        <display value="Fabry disease" />
      </concept>
      <concept>
        <code value="ORPHA:3240" />
        <display value="Central nervous system calcification-deafness-tubular acidosis-anemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3241" />
        <display value="Deafness-craniofacial syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3242" />
        <display value="Renpenning syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324262" />
        <display value="Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:324290" />
        <display value="Early-onset Lafora body disease" />
      </concept>
      <concept>
        <code value="ORPHA:324294" />
        <display value="T-cell immunodeficiency with epidermodysplasia verruciformis" />
      </concept>
      <concept>
        <code value="ORPHA:324299" />
        <display value="Multiple paragangliomas associated with polycythemia" />
      </concept>
      <concept>
        <code value="ORPHA:3243" />
        <display value="Sweet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324307" />
        <display value="Severe lateral tibial bowing with short stature" />
      </concept>
      <concept>
        <code value="ORPHA:324313" />
        <display value="9p13 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324321" />
        <display value="Sinoatrial node dysfunction and deafness" />
      </concept>
      <concept>
        <code value="ORPHA:324353" />
        <display value="Congenital achiasma" />
      </concept>
      <concept>
        <code value="ORPHA:324364" />
        <display value="Mixed sclerosing bone dystrophy with extra-skeletal manifestations" />
      </concept>
      <concept>
        <code value="ORPHA:324381" />
        <display value="Hereditary inclusion body myopathy type 4" />
      </concept>
      <concept>
        <code value="ORPHA:324410" />
        <display value="X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324416" />
        <display value="Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324422" />
        <display value="ALG13-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:324442" />
        <display value="Autosomal recessive axonal neuropathy with neuromyotonia" />
      </concept>
      <concept>
        <code value="ORPHA:324525" />
        <display value="Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation" />
      </concept>
      <concept>
        <code value="ORPHA:324530" />
        <display value="Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation" />
      </concept>
      <concept>
        <code value="ORPHA:324535" />
        <display value="Combined oxidative phosphorylation defect type 11" />
      </concept>
      <concept>
        <code value="ORPHA:324540" />
        <display value="Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324561" />
        <display value="Hypopigmentation-punctate palmoplantar keratoderma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324569" />
        <display value="Pontocerebellar hypoplasia type 8" />
      </concept>
      <concept>
        <code value="ORPHA:324575" />
        <display value="Hyperinsulinism due to HNF1A deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:324581" />
        <display value="Benign Samaritan congenital myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:324585" />
        <display value="Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain" />
      </concept>
      <concept>
        <code value="ORPHA:324588" />
        <display value="Familial dyskinesia and facial myokymia" />
      </concept>
      <concept>
        <code value="ORPHA:3246" />
        <display value="Symphalangism with multiple anomalies of hands and feet" />
      </concept>
      <concept>
        <code value="ORPHA:324601" />
        <display value="X-linked cleft palate and ankyloglossia" />
      </concept>
      <concept>
        <code value="ORPHA:324604" />
        <display value="Classic multiminicore myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:324611" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation" />
      </concept>
      <concept>
        <code value="ORPHA:324625" />
        <display value="Chikungunya" />
      </concept>
      <concept>
        <code value="ORPHA:324632" />
        <display value="Hendra virus infection" />
      </concept>
      <concept>
        <code value="ORPHA:324636" />
        <display value="Autoerythrocyte sensitization syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324648" />
        <display value="Invasive non-typhoidal salmonellosis" />
      </concept>
      <concept>
        <code value="ORPHA:324703" />
        <display value="ABetaL34V amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:324708" />
        <display value="ABeta amyloidosis, Iowa type" />
      </concept>
      <concept>
        <code value="ORPHA:324713" />
        <display value="ABeta amyloidosis, Italian type" />
      </concept>
      <concept>
        <code value="ORPHA:324718" />
        <display value="ABetaA21G amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:324723" />
        <display value="ABeta amyloidosis, Arctic type" />
      </concept>
      <concept>
        <code value="ORPHA:324737" />
        <display value="SRD5A3-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:324761" />
        <display value="Microcephalic primordial dwarfism" />
      </concept>
      <concept>
        <code value="ORPHA:324764" />
        <display value="Trichorhinophalangeal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324767" />
        <display value="Non-familial rare disease with dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:3248" />
        <display value="Distal symphalangism" />
      </concept>
      <concept>
        <code value="ORPHA:324924" />
        <display value="Hereditary periodic fever syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324927" />
        <display value="Pyogenic autoinflammatory syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324930" />
        <display value="Granulomatous autoinflammatory syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324933" />
        <display value="Mixed autoinflammatory and autoimmune syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324936" />
        <display value="Unclassified autoinflammatory syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324939" />
        <display value="Periodic fever syndrome of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:324942" />
        <display value="Pyogenic autoinflammatory syndrome of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:324950" />
        <display value="Granulomatous autoinflammatory syndrome of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:324953" />
        <display value="Unclassified autoinflammatory syndrome of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:324960" />
        <display value="Unexplained periodic fever syndrome of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:324964" />
        <display value="Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis" />
      </concept>
      <concept>
        <code value="ORPHA:324972" />
        <display value="MAGIC syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324977" />
        <display value="Proteasome disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:324999" />
        <display value="JMP syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:325" />
        <display value="Congenital factor II deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3250" />
        <display value="Proximal symphalangism" />
      </concept>
      <concept>
        <code value="ORPHA:325004" />
        <display value="CANDLE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:325055" />
        <display value="46,XX disorder of gonadal development" />
      </concept>
      <concept>
        <code value="ORPHA:325061" />
        <display value="46,XX disorder of sex development induced by fetoplacental androgens excess" />
      </concept>
      <concept>
        <code value="ORPHA:325093" />
        <display value="46,XX disorder of sex development induced by endogenous maternal-derived androgen" />
      </concept>
      <concept>
        <code value="ORPHA:325099" />
        <display value="46,XX disorder of sex development induced by exogenous maternal-derived androgen" />
      </concept>
      <concept>
        <code value="ORPHA:325109" />
        <display value="Syndrome with 46,XX disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:325118" />
        <display value="46,XY disorder of gonadal development" />
      </concept>
      <concept>
        <code value="ORPHA:325124" />
        <display value="Testicular agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:3253" />
        <display value="Zlotogora-Ogur syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:325345" />
        <display value="46,XY ovotesticular disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:325351" />
        <display value="46,XY disorder of sex development of endocrine origin" />
      </concept>
      <concept>
        <code value="ORPHA:325357" />
        <display value="46,XY disorder of sex development due to impaired androgen production" />
      </concept>
      <concept>
        <code value="ORPHA:325448" />
        <display value="Leydig cell hypoplasia due to LHB deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3255" />
        <display value="Filippi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:325511" />
        <display value="46,XY disorder of sex development due to a cholesterol synthesis defect" />
      </concept>
      <concept>
        <code value="ORPHA:325524" />
        <display value="Classic congenital lipoid adrenal hyperplasia due to STAR deficency" />
      </concept>
      <concept>
        <code value="ORPHA:325529" />
        <display value="Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency" />
      </concept>
      <concept>
        <code value="ORPHA:325537" />
        <display value="46,XY disorder of sex development induced by maternal exposure to endocrine disruptors" />
      </concept>
      <concept>
        <code value="ORPHA:325546" />
        <display value="Sex chromosome disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:325620" />
        <display value="Disorder of sex development of gynecological interest" />
      </concept>
      <concept>
        <code value="ORPHA:325632" />
        <display value="46,XY disorder of sex development of gynecological interest" />
      </concept>
      <concept>
        <code value="ORPHA:325638" />
        <display value="Syndrome with disorder of sex development of gynecological interest" />
      </concept>
      <concept>
        <code value="ORPHA:325665" />
        <display value="Genetic disorder of sex development of gynecological interest" />
      </concept>
      <concept>
        <code value="ORPHA:325690" />
        <display value="Genetic disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:325697" />
        <display value="Genetic 46,XX disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:325706" />
        <display value="Genetic 46,XY disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:325713" />
        <display value="Genetic 46,XY disorder of sex development of endocrine origin" />
      </concept>
      <concept>
        <code value="ORPHA:3258" />
        <display value="Cenani-Lenz syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3259" />
        <display value="Syndactyly-polydactyly-ear lobe syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:326" />
        <display value="Congenital factor V deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3260" />
        <display value="Idiopathic hypereosinophilic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3261" />
        <display value="Autoimmune lymphoproliferative syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3262" />
        <display value="Dobrow syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3263" />
        <display value="Syngnathia-cleft palate syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3265" />
        <display value="Humero-radial synostosis" />
      </concept>
      <concept>
        <code value="ORPHA:3266" />
        <display value="Humero-radio-ulnar synostosis" />
      </concept>
      <concept>
        <code value="ORPHA:3267" />
        <display value="Familial lambdoid synostosis" />
      </concept>
      <concept>
        <code value="ORPHA:3268" />
        <display value="Radioulnar synostosis-microcephaly-scoliosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3269" />
        <display value="Congenital radioulnar synostosis" />
      </concept>
      <concept>
        <code value="ORPHA:327" />
        <display value="Congenital factor VII deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3270" />
        <display value="Radioulnar synostosis-developmental delay-hypotonia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3273" />
        <display value="Synovial sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:3275" />
        <display value="Spondylocarpotarsal synostosis" />
      </concept>
      <concept>
        <code value="ORPHA:3276" />
        <display value="Disorder of plasmalogens biosynthesis" />
      </concept>
      <concept>
        <code value="ORPHA:328" />
        <display value="Congenital factor X deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3280" />
        <display value="Syringomyelia" />
      </concept>
      <concept>
        <code value="ORPHA:3282" />
        <display value="Multifocal atrial tachycardia" />
      </concept>
      <concept>
        <code value="ORPHA:3283" />
        <display value="His bundle tachycardia" />
      </concept>
      <concept>
        <code value="ORPHA:3286" />
        <display value="Catecholaminergic polymorphic ventricular tachycardia" />
      </concept>
      <concept>
        <code value="ORPHA:3287" />
        <display value="Takayasu arteritis" />
      </concept>
      <concept>
        <code value="ORPHA:3289" />
        <display value="Taurodontism" />
      </concept>
      <concept>
        <code value="ORPHA:329" />
        <display value="Congenital factor XI deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3291" />
        <display value="Teebi-Shaltout syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329173" />
        <display value="Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis" />
      </concept>
      <concept>
        <code value="ORPHA:329178" />
        <display value="Congenital muscular dystrophy with intellectual disability and severe epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:329191" />
        <display value="Tall stature-scoliosis-macrodactyly of the great toes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329195" />
        <display value="Developmental delay with autism spectrum disorder and gait instability" />
      </concept>
      <concept>
        <code value="ORPHA:3292" />
        <display value="Tel Hashomer camptodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329211" />
        <display value="Autosomal dominant neovascular inflammatory vitreoretinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:329217" />
        <display value="Cerebral sinovenous thrombosis" />
      </concept>
      <concept>
        <code value="ORPHA:329224" />
        <display value="Intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329228" />
        <display value="Microcephalic primordial dwarfism due to ZNF335 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:329235" />
        <display value="X-linked central congenital hypothyroidism with late-onset testicular enlargement" />
      </concept>
      <concept>
        <code value="ORPHA:329242" />
        <display value="Congenital chronic diarrhea with protein-losing enteropathy" />
      </concept>
      <concept>
        <code value="ORPHA:329249" />
        <display value="Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:329252" />
        <display value="Spondylocostal dysostosis-hypospadias-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329258" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2Q" />
      </concept>
      <concept>
        <code value="ORPHA:329284" />
        <display value="Beta-propeller protein-associated neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:3293" />
        <display value="Telecanthus-hypertelorism-strabismus-pes cavus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329303" />
        <display value="PLA2G6-associated neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:329308" />
        <display value="Fatty acid hydroxylase-associated neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:329314" />
        <display value="Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:329319" />
        <display value="Thrombocythemia with distal limb defects" />
      </concept>
      <concept>
        <code value="ORPHA:329324" />
        <display value="Inverse Klippel-Trenaunay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329329" />
        <display value="Autosomal recessive frontotemporal pachygyria" />
      </concept>
      <concept>
        <code value="ORPHA:329332" />
        <display value="Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329336" />
        <display value="Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:329341" />
        <display value="Limbic encephalitis with DPP6 antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:3294" />
        <display value="Extensor tendons of finger anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:329457" />
        <display value="Distal arthrogryposis type 5D" />
      </concept>
      <concept>
        <code value="ORPHA:329466" />
        <display value="Autosomal dominant focal dystonia, DYT25 type" />
      </concept>
      <concept>
        <code value="ORPHA:329469" />
        <display value="Acute megakaryoblastic leukemia without Down syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329475" />
        <display value="Spastic paraplegia-Paget disease of bone syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329478" />
        <display value="Adult-onset distal myopathy due to VCP mutation" />
      </concept>
      <concept>
        <code value="ORPHA:329481" />
        <display value="Lipoprotein glomerulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:32960" />
        <display value="Tumor necrosis factor receptor 1 associated periodic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329802" />
        <display value="5p13 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:329813" />
        <display value="Mosaic genome-wide paternal uniparental disomy" />
      </concept>
      <concept>
        <code value="ORPHA:329874" />
        <display value="Idiopathic giant cell myocarditis" />
      </concept>
      <concept>
        <code value="ORPHA:329883" />
        <display value="Non-hypoproteinemic hypertrophic gastropathy" />
      </concept>
      <concept>
        <code value="ORPHA:329888" />
        <display value="Juvenile idiopathic inflammatory myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:329894" />
        <display value="Juvenile overlap myositis" />
      </concept>
      <concept>
        <code value="ORPHA:3299" />
        <display value="Tetanus" />
      </concept>
      <concept>
        <code value="ORPHA:329903" />
        <display value="Immunoglobulin-mediated membranoproliferative glomerulonephritis" />
      </concept>
      <concept>
        <code value="ORPHA:329918" />
        <display value="Non-immunoglobulin-mediated membranoproliferative glomerulonephritis" />
      </concept>
      <concept>
        <code value="ORPHA:329931" />
        <display value="C3 glomerulonephritis" />
      </concept>
      <concept>
        <code value="ORPHA:329942" />
        <display value="Transient neonatal multiple acyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:329967" />
        <display value="Intermittent hydrarthrosis" />
      </concept>
      <concept>
        <code value="ORPHA:329971" />
        <display value="Generalized juvenile polyposis/juvenile polyposis coli" />
      </concept>
      <concept>
        <code value="ORPHA:329977" />
        <display value="Classic neuroendocrine tumor of appendix" />
      </concept>
      <concept>
        <code value="ORPHA:329984" />
        <display value="Goblet cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:33" />
        <display value="Isovaleric acidemia" />
      </concept>
      <concept>
        <code value="ORPHA:330" />
        <display value="Congenital factor XII deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:330001" />
        <display value="Wild type ATTR amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:33001" />
        <display value="Lymphedema-distichiasis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:330015" />
        <display value="Lead poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:330021" />
        <display value="Mercury poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:330029" />
        <display value="Hypotrichosis-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:330032" />
        <display value="Hemoglobin Lepore-beta-thalassemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:330041" />
        <display value="Hemoglobin M disease" />
      </concept>
      <concept>
        <code value="ORPHA:330050" />
        <display value="DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect" />
      </concept>
      <concept>
        <code value="ORPHA:330054" />
        <display value="Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:330058" />
        <display value="Hydroa vacciniforme" />
      </concept>
      <concept>
        <code value="ORPHA:330061" />
        <display value="Actinic prurigo" />
      </concept>
      <concept>
        <code value="ORPHA:330064" />
        <display value="Chronic actinic dermatitis" />
      </concept>
      <concept>
        <code value="ORPHA:3301" />
        <display value="Tetraamelia-multiple malformations syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:330197" />
        <display value="Genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:330206" />
        <display value="Genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:3303" />
        <display value="Tetralogy of Fallot" />
      </concept>
      <concept>
        <code value="ORPHA:3304" />
        <display value="Fallot complex-intellectual disability-growth delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3305" />
        <display value="Tetraploidy" />
      </concept>
      <concept>
        <code value="ORPHA:3306" />
        <display value="Duplication/inversion 15q11" />
      </concept>
      <concept>
        <code value="ORPHA:33067" />
        <display value="Metaphyseal chondrodysplasia, Jansen type" />
      </concept>
      <concept>
        <code value="ORPHA:33069" />
        <display value="Dravet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3307" />
        <display value="Tetrasomy 18p" />
      </concept>
      <concept>
        <code value="ORPHA:3309" />
        <display value="Tetrasomy 5p" />
      </concept>
      <concept>
        <code value="ORPHA:331" />
        <display value="Congenital factor XIII deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3310" />
        <display value="Tetrasomy 9p" />
      </concept>
      <concept>
        <code value="ORPHA:33108" />
        <display value="Lethal multiple pterygium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:33110" />
        <display value="Autosomal agammaglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:33111" />
        <display value="Granulomatous slack skin" />
      </concept>
      <concept>
        <code value="ORPHA:331176" />
        <display value="Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:331184" />
        <display value="Constitutional neutropenia with extra-hematopoietic manifestations" />
      </concept>
      <concept>
        <code value="ORPHA:331187" />
        <display value="Immunodeficiency due to MASP-2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:331190" />
        <display value="Immunodeficiency due to ficolin3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:331193" />
        <display value="Other immunodeficiency syndromes due to defects in innate immunity" />
      </concept>
      <concept>
        <code value="ORPHA:3312" />
        <display value="Thalidomide embryopathy" />
      </concept>
      <concept>
        <code value="ORPHA:331206" />
        <display value="Severe combined immunodeficiency due to complete RAG1/2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:331217" />
        <display value="Syndrome with combined immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:331220" />
        <display value="Immunodeficiency due to absence of thymus" />
      </concept>
      <concept>
        <code value="ORPHA:331223" />
        <display value="Hyper-IgE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:331226" />
        <display value="Susceptibility to infection due to TYK2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:331232" />
        <display value="Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells" />
      </concept>
      <concept>
        <code value="ORPHA:331235" />
        <display value="Selective IgM deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:331240" />
        <display value="Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells" />
      </concept>
      <concept>
        <code value="ORPHA:331244" />
        <display value="Other immunodeficiency syndrome with predominantly antibody defects" />
      </concept>
      <concept>
        <code value="ORPHA:331249" />
        <display value="Immunodeficiency syndrome with hypopigmentation" />
      </concept>
      <concept>
        <code value="ORPHA:3314" />
        <display value="Thiemann disease, familial form" />
      </concept>
      <concept>
        <code value="ORPHA:3316" />
        <display value="Thomas syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3317" />
        <display value="Thoracolaryngopelvic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:3318" />
        <display value="Essential thrombocythemia" />
      </concept>
      <concept>
        <code value="ORPHA:3319" />
        <display value="Congenital amegakaryocytic thrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:332" />
        <display value="Congenital intrinsic factor deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3320" />
        <display value="Thrombocytopenia-absent radius syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:33208" />
        <display value="Idiopathic hypersomnia" />
      </concept>
      <concept>
        <code value="ORPHA:3322" />
        <display value="Hoyeraal-Hreidarsson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:33226" />
        <display value="Waldenstrom macroglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:3323" />
        <display value="Thrombocytopenia-Robin sequence syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3324" />
        <display value="Familial thrombomodulin anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:3325" />
        <display value="Heparin-induced thrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:3326" />
        <display value="Thymic-renal-anal-lung dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:3327" />
        <display value="Thyrocerebrorenal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:33276" />
        <display value="Kaposi sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:3328" />
        <display value="Absent tibia-polydactyly-arachnoid cyst syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3329" />
        <display value="Tibial aplasia-ectrodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:333" />
        <display value="Farber disease" />
      </concept>
      <concept>
        <code value="ORPHA:33314" />
        <display value="Jessner lymphocytic infiltration of the skin" />
      </concept>
      <concept>
        <code value="ORPHA:3332" />
        <display value="Hypoplastic tibiae-postaxial polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:33355" />
        <display value="Reticular dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:33364" />
        <display value="Trichothiodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:3337" />
        <display value="Primary Fanconi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3338" />
        <display value="Toriello-Carey syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3339" />
        <display value="Toriello-Lacassie-Droste syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:334" />
        <display value="Familial atrial fibrillation" />
      </concept>
      <concept>
        <code value="ORPHA:33402" />
        <display value="Pediatric hepatocellular carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:33408" />
        <display value="Bullous lichen planus" />
      </concept>
      <concept>
        <code value="ORPHA:3341" />
        <display value="Torticollis-keloids-cryptorchidism-renal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3342" />
        <display value="Arterial tortuosity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3343" />
        <display value="Toxocariasis" />
      </concept>
      <concept>
        <code value="ORPHA:3344" />
        <display value="Weismann-Netter syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:33445" />
        <display value="Neuroectodermal melanolysosomal disease" />
      </concept>
      <concept>
        <code value="ORPHA:3346" />
        <display value="Tracheal agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:3347" />
        <display value="Mounier-Kuhn syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:33475" />
        <display value="Meningococcal meningitis" />
      </concept>
      <concept>
        <code value="ORPHA:3348" />
        <display value="Tracheobronchopathia osteochondroplastica" />
      </concept>
      <concept>
        <code value="ORPHA:335" />
        <display value="Congenital fibrinogen deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3350" />
        <display value="Tremor-nystagmus-duodenal ulcer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3351" />
        <display value="Trichodental syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3352" />
        <display value="Tricho-dento-osseous syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3353" />
        <display value="Trichodermodysplasia-dental alterations syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:33543" />
        <display value="Kleine-Levin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3355" />
        <display value="Trichoodontoonychial dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:33572" />
        <display value="5-oxoprolinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:33573" />
        <display value="Gamma-glutamyl transpeptidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:33574" />
        <display value="Glutamate-cysteine ligase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:33577" />
        <display value="Nodular non-suppurative panniculitis" />
      </concept>
      <concept>
        <code value="ORPHA:3361" />
        <display value="Trichodysplasia-xeroderma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3363" />
        <display value="Trichomegaly-retina pigmentary degeneration-dwarfism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3365" />
        <display value="Trigonocephaly-broad thumbs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3366" />
        <display value="Isolated trigonocephaly" />
      </concept>
      <concept>
        <code value="ORPHA:3368" />
        <display value="Trigonocephaly-bifid nose-acral anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3369" />
        <display value="Trigonocephaly-short stature-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:337" />
        <display value="Fibrodysplasia ossificans progressiva" />
      </concept>
      <concept>
        <code value="ORPHA:3374" />
        <display value="Triopia" />
      </concept>
      <concept>
        <code value="ORPHA:3375" />
        <display value="Trisomy X" />
      </concept>
      <concept>
        <code value="ORPHA:3376" />
        <display value="Triploidy" />
      </concept>
      <concept>
        <code value="ORPHA:3377" />
        <display value="Trismus-pseudocamptodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3378" />
        <display value="Trisomy 13" />
      </concept>
      <concept>
        <code value="ORPHA:3379" />
        <display value="Distal trisomy 17q" />
      </concept>
      <concept>
        <code value="ORPHA:338" />
        <display value="Familial multiple fibrofolliculoma" />
      </concept>
      <concept>
        <code value="ORPHA:3380" />
        <display value="Trisomy 18" />
      </concept>
      <concept>
        <code value="ORPHA:3383" />
        <display value="Humerus trochlea aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:3384" />
        <display value="Truncus arteriosus" />
      </concept>
      <concept>
        <code value="ORPHA:3385" />
        <display value="African trypanosomiasis" />
      </concept>
      <concept>
        <code value="ORPHA:3386" />
        <display value="American trypanosomiasis" />
      </concept>
      <concept>
        <code value="ORPHA:3387" />
        <display value="Isolated anterior cervical hypertrichosis" />
      </concept>
      <concept>
        <code value="ORPHA:3388" />
        <display value="Neural tube defect" />
      </concept>
      <concept>
        <code value="ORPHA:3389" />
        <display value="Tuberculosis" />
      </concept>
      <concept>
        <code value="ORPHA:3390" />
        <display value="Proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3392" />
        <display value="Tularemia" />
      </concept>
      <concept>
        <code value="ORPHA:3394" />
        <display value="Soft tissue sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:3398" />
        <display value="Thymic epithelial neoplasm" />
      </concept>
      <concept>
        <code value="ORPHA:3399" />
        <display value="Germ cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:340" />
        <display value="Hemorrhagic fever-renal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3400" />
        <display value="Aorto-ventricular tunnel" />
      </concept>
      <concept>
        <code value="ORPHA:3402" />
        <display value="Transient tyrosinemia of the newborn" />
      </concept>
      <concept>
        <code value="ORPHA:3403" />
        <display value="Uhl anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:3404" />
        <display value="Ulbright-Hodes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3405" />
        <display value="Umbilical cord ulceration-intestinal atresia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3406" />
        <display value="Ulerythema ophryogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:3408" />
        <display value="Upington disease" />
      </concept>
      <concept>
        <code value="ORPHA:3409" />
        <display value="Urban-Rogers-Meyer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:341" />
        <display value="Viral hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:3411" />
        <display value="Double uterus-hemivagina-renal agenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3412" />
        <display value="VACTERL with hydrocephalus" />
      </concept>
      <concept>
        <code value="ORPHA:34149" />
        <display value="Autosomal dominant tubulointerstitial kidney disease" />
      </concept>
      <concept>
        <code value="ORPHA:3416" />
        <display value="Hyperostosis corticalis generalisata" />
      </concept>
      <concept>
        <code value="ORPHA:3417" />
        <display value="Van den Bosch syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:342" />
        <display value="Familial Mediterranean fever" />
      </concept>
      <concept>
        <code value="ORPHA:34217" />
        <display value="Naxos disease" />
      </concept>
      <concept>
        <code value="ORPHA:3424" />
        <display value="Velo-facial-skeletal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3426" />
        <display value="Double outlet right ventricle" />
      </concept>
      <concept>
        <code value="ORPHA:3427" />
        <display value="Double outlet left ventricle" />
      </concept>
      <concept>
        <code value="ORPHA:3429" />
        <display value="Verloove Vanhorick-Brubakk syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:343" />
        <display value="Hyperimmunoglobulinemia D with periodic fever" />
      </concept>
      <concept>
        <code value="ORPHA:3433" />
        <display value="Microcephaly-brachydactyly-kyphoscoliosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3434" />
        <display value="MMEP syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3437" />
        <display value="Vogt-Koyanagi-Harada disease" />
      </concept>
      <concept>
        <code value="ORPHA:3439" />
        <display value="Von Voss-Cherstvoy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:344" />
        <display value="Arbovirus fever" />
      </concept>
      <concept>
        <code value="ORPHA:3440" />
        <display value="Waardenburg syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3447" />
        <display value="Weaver syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3448" />
        <display value="Weaver-Williams syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3449" />
        <display value="Weill-Marchesani syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:345" />
        <display value="Dissecting cellulitis of the scalp" />
      </concept>
      <concept>
        <code value="ORPHA:3450" />
        <display value="Weissenbacher- Zweymuller syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3451" />
        <display value="West syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:34514" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2G" />
      </concept>
      <concept>
        <code value="ORPHA:34515" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2I" />
      </concept>
      <concept>
        <code value="ORPHA:34516" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy type 1D" />
      </concept>
      <concept>
        <code value="ORPHA:34517" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy type 1E" />
      </concept>
      <concept>
        <code value="ORPHA:3452" />
        <display value="Whipple disease" />
      </concept>
      <concept>
        <code value="ORPHA:34520" />
        <display value="Congenital muscular dystrophy with integrin alpha-7 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:34526" />
        <display value="Familial primary hypomagnesemia" />
      </concept>
      <concept>
        <code value="ORPHA:34527" />
        <display value="Familial primary hypomagnesemia with normocalciuria and normocalcemia" />
      </concept>
      <concept>
        <code value="ORPHA:34528" />
        <display value="Autosomal dominant primary hypomagnesemia with hypocalciuria" />
      </concept>
      <concept>
        <code value="ORPHA:3453" />
        <display value="Autoimmune polyendocrinopathy type 1" />
      </concept>
      <concept>
        <code value="ORPHA:34533" />
        <display value="Corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:3454" />
        <display value="Intellectual disability-developmental delay-contractures syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3455" />
        <display value="Wiedemann-Rautenstrauch syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3456" />
        <display value="Wildervanck syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:34587" />
        <display value="Glycogen storage disease due to LAMP-2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:3459" />
        <display value="Wilson-Turner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:34592" />
        <display value="Immunodeficiency by defective expression of HLA class 1" />
      </concept>
      <concept>
        <code value="ORPHA:346" />
        <display value="Quinquauds folliculitis decalvans" />
      </concept>
      <concept>
        <code value="ORPHA:3460" />
        <display value="Torg-Winchester syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3463" />
        <display value="Wolfram syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3464" />
        <display value="Woodhouse-Sakati syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3465" />
        <display value="Worster-Drought syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3466" />
        <display value="WT limb-blood syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3467" />
        <display value="Hereditary xanthinuria" />
      </concept>
      <concept>
        <code value="ORPHA:3469" />
        <display value="XK aprosencephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:347" />
        <display value="Frasier syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3471" />
        <display value="Young syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3472" />
        <display value="Yunis-Varon syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3473" />
        <display value="Zimmermann-Laband syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:3474" />
        <display value="CHIME syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:348" />
        <display value="Fructose-1,6-bisphosphatase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:349" />
        <display value="Fucosidosis" />
      </concept>
      <concept>
        <code value="ORPHA:35" />
        <display value="Propionic acidemia" />
      </concept>
      <concept>
        <code value="ORPHA:35061" />
        <display value="Idiopathic recurrent and disabling cutaneous herpes" />
      </concept>
      <concept>
        <code value="ORPHA:35062" />
        <display value="Idiopathic disseminated cytomegalovirus infection" />
      </concept>
      <concept>
        <code value="ORPHA:35063" />
        <display value="Fulminant viral hepatitis" />
      </concept>
      <concept>
        <code value="ORPHA:35065" />
        <display value="Idiopathic severe pneumococcemia" />
      </concept>
      <concept>
        <code value="ORPHA:35069" />
        <display value="Infantile neuroaxonal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:35078" />
        <display value="T-B+ severe combined immunodeficiency due to JAK3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:35093" />
        <display value="Isolated scaphocephaly" />
      </concept>
      <concept>
        <code value="ORPHA:35098" />
        <display value="Isolated plagiocephaly" />
      </concept>
      <concept>
        <code value="ORPHA:35099" />
        <display value="Isolated brachycephaly" />
      </concept>
      <concept>
        <code value="ORPHA:351" />
        <display value="Galactosialidosis" />
      </concept>
      <concept>
        <code value="ORPHA:35107" />
        <display value="Desmosterolosis" />
      </concept>
      <concept>
        <code value="ORPHA:35120" />
        <display value="Hemolytic anemia due to pyrimidine 5 nucleotidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:35121" />
        <display value="Lysosomal acid phosphatase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:35122" />
        <display value="Congenital sucrase-isomaltase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:35125" />
        <display value="Epidermal nevus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:35173" />
        <display value="X-linked dominant chondrodysplasia punctata" />
      </concept>
      <concept>
        <code value="ORPHA:352" />
        <display value="Galactosemia" />
      </concept>
      <concept>
        <code value="ORPHA:352298" />
        <display value="Genetic muscular channelopathy" />
      </concept>
      <concept>
        <code value="ORPHA:352301" />
        <display value="Disorder of phospholipids, sphingolipids and fatty acids biosynthesis" />
      </concept>
      <concept>
        <code value="ORPHA:352306" />
        <display value="Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement" />
      </concept>
      <concept>
        <code value="ORPHA:352309" />
        <display value="Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with peripheral nerves predominant involvement" />
      </concept>
      <concept>
        <code value="ORPHA:352312" />
        <display value="Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement" />
      </concept>
      <concept>
        <code value="ORPHA:352328" />
        <display value="MEGDEL syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352333" />
        <display value="Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352403" />
        <display value="Spectrin-associated autosomal recessive cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:352447" />
        <display value="Progressive external ophthalmoplegia-myopathy-emaciation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352456" />
        <display value="Mitochondrial DNA maintenance syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352470" />
        <display value="Mitochondrial DNA deletion syndrome with progressive myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:352479" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2U" />
      </concept>
      <concept>
        <code value="ORPHA:352487" />
        <display value="Digital anomalies-intellectual disability-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352490" />
        <display value="Autism spectrum disorder due to AUTS2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:352530" />
        <display value="Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352540" />
        <display value="Oncogenic osteomalacia" />
      </concept>
      <concept>
        <code value="ORPHA:352563" />
        <display value="Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:352577" />
        <display value="Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352582" />
        <display value="Familial infantile myoclonic epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:352587" />
        <display value="Focal epilepsy-intellectual disability-cerebro-cerebellar malformation" />
      </concept>
      <concept>
        <code value="ORPHA:352596" />
        <display value="Progressive myoclonic epilepsy with dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:352629" />
        <display value="16q24.1 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352636" />
        <display value="Phalangeal microgeodic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352641" />
        <display value="Autosomal recessive cerebellar ataxia with late-onset spasticity" />
      </concept>
      <concept>
        <code value="ORPHA:352649" />
        <display value="Brain dopamine-serotonin vesicular transport disease" />
      </concept>
      <concept>
        <code value="ORPHA:352654" />
        <display value="Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352657" />
        <display value="Hereditary benign intraepithelial dyskeratosis" />
      </concept>
      <concept>
        <code value="ORPHA:352662" />
        <display value="Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352665" />
        <display value="Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:352670" />
        <display value="Autosomal dominant intermediate Charcot-Marie-Tooth disease type F" />
      </concept>
      <concept>
        <code value="ORPHA:352675" />
        <display value="X-linked Charcot-Marie-Tooth disease type 6" />
      </concept>
      <concept>
        <code value="ORPHA:352682" />
        <display value="Cobblestone lissencephaly without muscular or ocular involvement" />
      </concept>
      <concept>
        <code value="ORPHA:352687" />
        <display value="Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:352709" />
        <display value="CLN13 disease" />
      </concept>
      <concept>
        <code value="ORPHA:352712" />
        <display value="Facial dysmorphism-immunodeficiency-livedo-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352718" />
        <display value="Progressive retinal dystrophy due to retinol transport defect" />
      </concept>
      <concept>
        <code value="ORPHA:352723" />
        <display value="Attenuated Chediak-Higashi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:352728" />
        <display value="Disorder of melanin metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:352731" />
        <display value="Oculocutaneous albinism type 1" />
      </concept>
      <concept>
        <code value="ORPHA:352734" />
        <display value="Minimal pigment oculocutaneous albinism type 1" />
      </concept>
      <concept>
        <code value="ORPHA:352737" />
        <display value="Temperature-sensitive oculocutaneous albinism type 1" />
      </concept>
      <concept>
        <code value="ORPHA:352740" />
        <display value="Ocular albinism with congenital sensorineural deafness" />
      </concept>
      <concept>
        <code value="ORPHA:352745" />
        <display value="Oculocutaneous albinism type 7" />
      </concept>
      <concept>
        <code value="ORPHA:352763" />
        <display value="Scleredema" />
      </concept>
      <concept>
        <code value="ORPHA:353" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2C" />
      </concept>
      <concept>
        <code value="ORPHA:353217" />
        <display value="Epileptic encephalopathy with global cerebral demyelination" />
      </concept>
      <concept>
        <code value="ORPHA:353220" />
        <display value="Familial primary localized cutaneous amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:353253" />
        <display value="Burning mouth syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:353277" />
        <display value="Rubinstein-Taybi syndrome due to CREBBP mutations" />
      </concept>
      <concept>
        <code value="ORPHA:353281" />
        <display value="Rubinstein-Taybi syndrome due to 16p13.3 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:353284" />
        <display value="Rubinstein-Taybi syndrome due to EP300 haploinsufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:353298" />
        <display value="Roifman syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:353308" />
        <display value="Pyruvate carboxylase deficiency, infantile type" />
      </concept>
      <concept>
        <code value="ORPHA:353314" />
        <display value="Pyruvate carboxylase deficiency, severe neonatal type" />
      </concept>
      <concept>
        <code value="ORPHA:353320" />
        <display value="Pyruvate carboxylase deficiency, benign type" />
      </concept>
      <concept>
        <code value="ORPHA:353327" />
        <display value="Congenital myasthenic syndromes with glycosylation defect" />
      </concept>
      <concept>
        <code value="ORPHA:353334" />
        <display value="Congenital retinal arteriovenous communication" />
      </concept>
      <concept>
        <code value="ORPHA:353344" />
        <display value="Idiopathic macular telangiectasia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:353351" />
        <display value="Idiopathic macular telangiectasia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:353356" />
        <display value="Vasoproliferative tumor of the retina" />
      </concept>
      <concept>
        <code value="ORPHA:354" />
        <display value="GM1 gangliosidosis" />
      </concept>
      <concept>
        <code value="ORPHA:355" />
        <display value="Gaucher disease" />
      </concept>
      <concept>
        <code value="ORPHA:356" />
        <display value="Gerstmann-Straussler-Scheinker syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:35612" />
        <display value="Nanophthalmia" />
      </concept>
      <concept>
        <code value="ORPHA:35656" />
        <display value="Coenzyme Q10 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:35664" />
        <display value="ALDH18A1-related De Barsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:35686" />
        <display value="Serpiginous choroiditis" />
      </concept>
      <concept>
        <code value="ORPHA:35687" />
        <display value="Erdheim-Chester disease" />
      </concept>
      <concept>
        <code value="ORPHA:35688" />
        <display value="Madelung deformity" />
      </concept>
      <concept>
        <code value="ORPHA:35689" />
        <display value="Primary lateral sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:356947" />
        <display value="3q26q27 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:35696" />
        <display value="Mitochondrial disorder due to a defect in mitochondrial protein synthesis" />
      </concept>
      <concept>
        <code value="ORPHA:356961" />
        <display value="SLC35A2-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:356978" />
        <display value="D,L-2-hydroxyglutaric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:35698" />
        <display value="Mitochondrial DNA depletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:356996" />
        <display value="Intellectual disability-hypotonia-spasticity-sleep disorder syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:357001" />
        <display value="19p13.13 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:357008" />
        <display value="Atypical hemolytic-uremic syndrome with DGKE deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:35701" />
        <display value="3-hydroxy-3-methylglutaryl-CoA synthase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:357027" />
        <display value="Hereditary retinoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:357034" />
        <display value="Non-hereditary retinoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:35704" />
        <display value="L-Arginine:glycine amidinotransferase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:357043" />
        <display value="Amyotrophic lateral sclerosis type 4" />
      </concept>
      <concept>
        <code value="ORPHA:35705" />
        <display value="Neurometabolic disorder due to serine deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:357058" />
        <display value="Autosomal recessive cutis laxa type 2A" />
      </concept>
      <concept>
        <code value="ORPHA:35706" />
        <display value="Glutaric acidemia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:357064" />
        <display value="Autosomal recessive cutis laxa type 2B" />
      </concept>
      <concept>
        <code value="ORPHA:357074" />
        <display value="Autosomal recessive cutis laxa type 2, classic type" />
      </concept>
      <concept>
        <code value="ORPHA:35708" />
        <display value="Aromatic L-amino acid decarboxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:35710" />
        <display value="Glucose-galactose malabsorption" />
      </concept>
      <concept>
        <code value="ORPHA:357107" />
        <display value="Arterial thoracic outlet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:357131" />
        <display value="Venous thoracic outlet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:357154" />
        <display value="Oral submucous fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:357158" />
        <display value="Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:357175" />
        <display value="Short ulna-dysmorphism-hypotonia-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:357220" />
        <display value="Primary essential cutis verticis gyrata" />
      </concept>
      <concept>
        <code value="ORPHA:357225" />
        <display value="Primary non-essential cutis verticis gyrata" />
      </concept>
      <concept>
        <code value="ORPHA:357237" />
        <display value="Severe combined immunodeficiency due to CARD11 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:357329" />
        <display value="Combined immunodeficiency due to IL21R deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:357332" />
        <display value="Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:35737" />
        <display value="Morning glory syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:357502" />
        <display value="Idiopathic nephrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:357506" />
        <display value="Genetic non-syndromic renal or urinary tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:358" />
        <display value="Gitelman syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:35807" />
        <display value="Malignant germ cell tumor of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:35808" />
        <display value="Malignant sex cord stromal tumor of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:35858" />
        <display value="Grasbeck-Imerslund disease" />
      </concept>
      <concept>
        <code value="ORPHA:35878" />
        <display value="Hyperinsulinism-hyperammonemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:35889" />
        <display value="Acute opioid poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:359" />
        <display value="Hereditary glaucoma" />
      </concept>
      <concept>
        <code value="ORPHA:35909" />
        <display value="Combined deficiency of factor V and factor VIII" />
      </concept>
      <concept>
        <code value="ORPHA:35981" />
        <display value="Polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:36" />
        <display value="Acrocallosal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:360" />
        <display value="Glioblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:361" />
        <display value="Familial glucocorticoid deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:36204" />
        <display value="Intestinal lymphangiectasia" />
      </concept>
      <concept>
        <code value="ORPHA:36234" />
        <display value="Bacterial toxic-shock syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:36235" />
        <display value="Staphylococcal scarlet fever" />
      </concept>
      <concept>
        <code value="ORPHA:36236" />
        <display value="Staphylococcal scalded skin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:36237" />
        <display value="Bullous impetigo" />
      </concept>
      <concept>
        <code value="ORPHA:36238" />
        <display value="Staphylococcal necrotizing pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:36258" />
        <display value="Buerger disease" />
      </concept>
      <concept>
        <code value="ORPHA:36273" />
        <display value="Gastric linitis plastica" />
      </concept>
      <concept>
        <code value="ORPHA:363189" />
        <display value="Congenital anomaly of the great veins" />
      </concept>
      <concept>
        <code value="ORPHA:363203" />
        <display value="Ring chromosome" />
      </concept>
      <concept>
        <code value="ORPHA:363245" />
        <display value="Genetic progeroid syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363294" />
        <display value="Genetic syndromic Pierre Robin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363300" />
        <display value="Genetic intractable diarrhea of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:363306" />
        <display value="Genetic intestinal disease due to fat malabsorption" />
      </concept>
      <concept>
        <code value="ORPHA:363314" />
        <display value="Genetic intestinal polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:363396" />
        <display value="High myopia-sensorineural deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363400" />
        <display value="Severe neurodegenerative syndrome with lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:363409" />
        <display value="Fetal akinesia-cerebral and retinal hemorrhage syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363412" />
        <display value="Hypomyelination with brain stem and spinal cord involvement and leg spasticity" />
      </concept>
      <concept>
        <code value="ORPHA:363417" />
        <display value="Temtamy preaxial brachydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363424" />
        <display value="Multiple mitochondrial dysfunctions syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:363429" />
        <display value="Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363432" />
        <display value="Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:363444" />
        <display value="THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363447" />
        <display value="Autosomal dominant childhood-onset proximal spinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:363454" />
        <display value="Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures" />
      </concept>
      <concept>
        <code value="ORPHA:363472" />
        <display value="Tumor of testis and paratestis" />
      </concept>
      <concept>
        <code value="ORPHA:363478" />
        <display value="Paratesticular adenocarcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:363483" />
        <display value="Testicular teratoma" />
      </concept>
      <concept>
        <code value="ORPHA:363489" />
        <display value="Sex cord-stromal tumor of testis" />
      </concept>
      <concept>
        <code value="ORPHA:363494" />
        <display value="Non-seminomatous germ cell tumor of testis" />
      </concept>
      <concept>
        <code value="ORPHA:363504" />
        <display value="Germ cell tumor of testis" />
      </concept>
      <concept>
        <code value="ORPHA:363523" />
        <display value="Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363528" />
        <display value="Intellectual disability-strabismus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363534" />
        <display value="Mitochondrial DNA depletion syndrome, hepatocerebrorenal form" />
      </concept>
      <concept>
        <code value="ORPHA:363540" />
        <display value="Leukoencephalopathy with mild cerebellar ataxia and white matter edema" />
      </concept>
      <concept>
        <code value="ORPHA:363543" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2R" />
      </concept>
      <concept>
        <code value="ORPHA:363549" />
        <display value="Acute encephalopathy with biphasic seizures and late reduced diffusion" />
      </concept>
      <concept>
        <code value="ORPHA:36355" />
        <display value="P2Y12 defect" />
      </concept>
      <concept>
        <code value="ORPHA:363558" />
        <display value="New-onset refractory status epilepticus" />
      </concept>
      <concept>
        <code value="ORPHA:363567" />
        <display value="Acute encephalopathy with inflammation-mediated status epilepticus" />
      </concept>
      <concept>
        <code value="ORPHA:363579" />
        <display value="Extragonadal germ cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:363582" />
        <display value="Gonadal germ cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:363611" />
        <display value="Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363618" />
        <display value="LMNA-related cardiocutaneous progeria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363623" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2T" />
      </concept>
      <concept>
        <code value="ORPHA:363649" />
        <display value="Mandibular hypoplasia-deafness-progeroid syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363654" />
        <display value="X-linked parkinsonism-spasticity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363659" />
        <display value="20q11.2 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363665" />
        <display value="Acroosteolysis-keloid-like lesions-premature aging syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:36367" />
        <display value="Distal monosomy 1q" />
      </concept>
      <concept>
        <code value="ORPHA:363677" />
        <display value="Childhood-onset autosomal recessive myopathy with external ophthalmoplegia" />
      </concept>
      <concept>
        <code value="ORPHA:363680" />
        <display value="2p13.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363686" />
        <display value="Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363694" />
        <display value="Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363700" />
        <display value="Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion" />
      </concept>
      <concept>
        <code value="ORPHA:363705" />
        <display value="Craniofaciofrontodigital syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363710" />
        <display value="Spinocerebellar ataxia type 37" />
      </concept>
      <concept>
        <code value="ORPHA:363717" />
        <display value="Alexander disease type I" />
      </concept>
      <concept>
        <code value="ORPHA:363722" />
        <display value="Alexander disease type II" />
      </concept>
      <concept>
        <code value="ORPHA:363727" />
        <display value="X-linked dyserythropoietic anemia with abnormal platelets and neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:363741" />
        <display value="Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363746" />
        <display value="Balint syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:36382" />
        <display value="Familial cervical artery dissection" />
      </concept>
      <concept>
        <code value="ORPHA:36383" />
        <display value="COL4A1-related familial vascular leukoencephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:36386" />
        <display value="Hereditary sensory and autonomic neuropathy type 1" />
      </concept>
      <concept>
        <code value="ORPHA:36387" />
        <display value="Generalized epilepsy with febrile seizures-plus" />
      </concept>
      <concept>
        <code value="ORPHA:36388" />
        <display value="Paraneoplastic neurologic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363958" />
        <display value="17q21.31 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363965" />
        <display value="Koolen-De Vries syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:363969" />
        <display value="Autosomal recessive cerebral atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:36397" />
        <display value="Adiposis dolorosa" />
      </concept>
      <concept>
        <code value="ORPHA:363972" />
        <display value="Noonan syndrome-like disorder with juvenile myelomonocytic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:363976" />
        <display value="Giant cell tumor of bone" />
      </concept>
      <concept>
        <code value="ORPHA:363981" />
        <display value="Charcot-Marie-Tooth disease type 4B3" />
      </concept>
      <concept>
        <code value="ORPHA:363989" />
        <display value="Familial benign flecked retina" />
      </concept>
      <concept>
        <code value="ORPHA:363992" />
        <display value="Ichthyosis-short stature-brachydactyly-microspherophakia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:363999" />
        <display value="Non-immune hydrops fetalis" />
      </concept>
      <concept>
        <code value="ORPHA:364" />
        <display value="Glycogen storage disease due to glucose-6-phosphatase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:364013" />
        <display value="Immune hydrops fetalis" />
      </concept>
      <concept>
        <code value="ORPHA:364028" />
        <display value="X-linked intellectual disability due to GRIA3 mutations" />
      </concept>
      <concept>
        <code value="ORPHA:364033" />
        <display value="Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:364039" />
        <display value="Hydroa vacciniforme-like lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:364043" />
        <display value="ALK-positive large B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:364055" />
        <display value="Severe early-childhood-onset retinal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:364063" />
        <display value="Infantile epileptic-dyskinetic encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:36412" />
        <display value="Hypocomplementemic urticarial vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:364198" />
        <display value="Bipartite talus" />
      </concept>
      <concept>
        <code value="ORPHA:36426" />
        <display value="Stevens-Johnson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:364526" />
        <display value="Primary bone dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:364531" />
        <display value="Primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments" />
      </concept>
      <concept>
        <code value="ORPHA:364536" />
        <display value="Primary bone dysplasia with micromelia" />
      </concept>
      <concept>
        <code value="ORPHA:364541" />
        <display value="Otopalatodigital syndrome spectrum disorder" />
      </concept>
      <concept>
        <code value="ORPHA:364559" />
        <display value="Dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:364568" />
        <display value="Dysostosis with limb anomaly as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:364571" />
        <display value="Dysostosis with limb and face anomalies as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:364574" />
        <display value="Acrofacial dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:364577" />
        <display value="Intellectual disability-brachydactyly-Pierre Robin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:364803" />
        <display value="Rare bone disease related to a common gene or pathway defect" />
      </concept>
      <concept>
        <code value="ORPHA:364817" />
        <display value="Aggrecan-related bone disorder" />
      </concept>
      <concept>
        <code value="ORPHA:364820" />
        <display value="TRPV4-related bone disorder" />
      </concept>
      <concept>
        <code value="ORPHA:365" />
        <display value="Glycogen storage disease due to acid maltase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:365563" />
        <display value="Primary short bowel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:366" />
        <display value="Glycogen storage disease due to glycogen debranching enzyme deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:367" />
        <display value="Glycogen storage disease due to glycogen branching enzyme deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:368" />
        <display value="Glycogen storage disease due to muscle glycogen phosphorylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:36899" />
        <display value="Myoclonus-dystonia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369" />
        <display value="Glycogen storage disease due to liver glycogen phosphorylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:36913" />
        <display value="Autoimmune hypoparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:369837" />
        <display value="Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369840" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2S" />
      </concept>
      <concept>
        <code value="ORPHA:369847" />
        <display value="Intellectual disability-hyperkinetic movement-truncal ataxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369852" />
        <display value="Congenital neutropenia-myelofibrosis-nephromegaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369861" />
        <display value="Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369867" />
        <display value="Autosomal recessive intermediate Charcot-Marie-Tooth disease type C" />
      </concept>
      <concept>
        <code value="ORPHA:369873" />
        <display value="Obesity due to SIM1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:369881" />
        <display value="2p21 microdeletion syndrome without cystinuria" />
      </concept>
      <concept>
        <code value="ORPHA:369886" />
        <display value="Homozygous 2p21 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369891" />
        <display value="Cardiac anomalies-developmental delay-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369897" />
        <display value="Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:369913" />
        <display value="Combined oxidative phosphorylation defect type 17" />
      </concept>
      <concept>
        <code value="ORPHA:369920" />
        <display value="Pontocerebellar hypoplasia type 9" />
      </concept>
      <concept>
        <code value="ORPHA:369929" />
        <display value="Primary hyperaldosteronism-seizures-neurological abnormalities syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369939" />
        <display value="Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369942" />
        <display value="CADDS" />
      </concept>
      <concept>
        <code value="ORPHA:369950" />
        <display value="Intellectual disability-seizures-macrocephaly-obesity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369955" />
        <display value="Methylmalonic acidemia with homocystinuria, type cblJ" />
      </concept>
      <concept>
        <code value="ORPHA:369962" />
        <display value="Methylmalonic acidemia with homocystinuria, type cblX" />
      </concept>
      <concept>
        <code value="ORPHA:369970" />
        <display value="Microcornea-myopic chorioretinal atrophy-telecanthus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369979" />
        <display value="Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369992" />
        <display value="Severe dermatitis-multiple allergies-metabolic wasting syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:369999" />
        <display value="Diffuse palmoplantar keratoderma with painful fissures" />
      </concept>
      <concept>
        <code value="ORPHA:37" />
        <display value="Acrodermatitis enteropathica" />
      </concept>
      <concept>
        <code value="ORPHA:370" />
        <display value="Glycogen storage disease due to phosphorylase kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:370002" />
        <display value="Focal palmoplantar keratoderma with joint keratoses" />
      </concept>
      <concept>
        <code value="ORPHA:370010" />
        <display value="Intellectual disability-facial dysmorphism-hand anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370015" />
        <display value="Spondyloepimetaphyseal dysplasia, Isidor type" />
      </concept>
      <concept>
        <code value="ORPHA:370019" />
        <display value="Spondylometaphyseal dysplasia, Czarny-Ratajczak type" />
      </concept>
      <concept>
        <code value="ORPHA:370022" />
        <display value="Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370026" />
        <display value="Acute myeloid leukemia with t(8;16)(p11;p13) translocation" />
      </concept>
      <concept>
        <code value="ORPHA:370034" />
        <display value="Familial syringomyelia" />
      </concept>
      <concept>
        <code value="ORPHA:370039" />
        <display value="Angora hair nevus" />
      </concept>
      <concept>
        <code value="ORPHA:370046" />
        <display value="Didymosis aplasticosebacea" />
      </concept>
      <concept>
        <code value="ORPHA:370052" />
        <display value="SCALP syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370059" />
        <display value="NEVADA syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370068" />
        <display value="Fetal anticonvulsant syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370076" />
        <display value="Fetal carbamazepine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370079" />
        <display value="Proximal 16p11.2 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370088" />
        <display value="Acute infantile liver failure-multisystemic involvement syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370091" />
        <display value="Oculocutaneous albinism type 5" />
      </concept>
      <concept>
        <code value="ORPHA:370097" />
        <display value="Oculocutaneous albinism type 6" />
      </concept>
      <concept>
        <code value="ORPHA:370103" />
        <display value="Primary dystonia, DYT17 type" />
      </concept>
      <concept>
        <code value="ORPHA:370106" />
        <display value="Rare disorder with dystonia and other neurologic or systemic manifestation" />
      </concept>
      <concept>
        <code value="ORPHA:370109" />
        <display value="Ataxia-telangiectasia variant" />
      </concept>
      <concept>
        <code value="ORPHA:370114" />
        <display value="Combined cervical dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:370127" />
        <display value="Medich giant platelet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370131" />
        <display value="White platelet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370334" />
        <display value="Extraskeletal Ewing sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:370348" />
        <display value="Peripheral primitive neuroectodermal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:370396" />
        <display value="Small cell carcinoma of the ovary" />
      </concept>
      <concept>
        <code value="ORPHA:37042" />
        <display value="Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370921" />
        <display value="STT3A-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:370924" />
        <display value="STT3B-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:370927" />
        <display value="SSR4-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:370930" />
        <display value="XYLT1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:370933" />
        <display value="GM3 synthase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:370938" />
        <display value="Salt-and-pepper syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370943" />
        <display value="Autism spectrum disorder-epilepsy-arthrogryposis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:370953" />
        <display value="Congenital muscular dystrophy due to dystroglycanopathy" />
      </concept>
      <concept>
        <code value="ORPHA:370959" />
        <display value="Congenital muscular dystrophy with cerebellar involvement" />
      </concept>
      <concept>
        <code value="ORPHA:370968" />
        <display value="Congenital muscular dystrophy with intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:370980" />
        <display value="Congenital muscular dystrophy without intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:370997" />
        <display value="Muscle-eye-brain disease with bilateral multicystic leucodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:371" />
        <display value="Glycogen storage disease due to muscle phosphofructokinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:371007" />
        <display value="Congenital muscular dystrophy with hyperlaxity" />
      </concept>
      <concept>
        <code value="ORPHA:371024" />
        <display value="Qualitative or quantitative defects of alpha-dystroglycan" />
      </concept>
      <concept>
        <code value="ORPHA:371040" />
        <display value="Primary qualitative or quantitative defects of alpha-dystroglycan" />
      </concept>
      <concept>
        <code value="ORPHA:371047" />
        <display value="Congenital disorder of glycosylation with neurological involvement" />
      </concept>
      <concept>
        <code value="ORPHA:371054" />
        <display value="X-linked congenital disorder of glycosylation with intellectual disability as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:371064" />
        <display value="Non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:371071" />
        <display value="Congenital disorder of glycosylation with epilepsy as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:371157" />
        <display value="Congenital disorder of glycosylation with hepatic involvement" />
      </concept>
      <concept>
        <code value="ORPHA:371176" />
        <display value="Congenital disorder of glycosylation with dilated cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:371183" />
        <display value="Congenital disorder of glycosylation with cardiac malformation as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:371188" />
        <display value="Congenital disorder of glycosylation with intestinal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:371195" />
        <display value="Congenital disorder of glycosylation-related bone disorder" />
      </concept>
      <concept>
        <code value="ORPHA:371200" />
        <display value="Congenital disorder of glycosylation with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:371207" />
        <display value="Congenital disorder of glycosylation with nephropathy as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:371212" />
        <display value="Congenital disorder of glycosylation with deafness as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:371235" />
        <display value="Congenital disorder of glycosylation with developmental anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:371364" />
        <display value="Hypotonia-speech impairment-severe cognitive delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:371428" />
        <display value="Multicentric osteolysis-nodulosis-arthropathy spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:371433" />
        <display value="Genetic periodic paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:371436" />
        <display value="Genetic neurovascular malformation" />
      </concept>
      <concept>
        <code value="ORPHA:371442" />
        <display value="Sphingolipidosis with epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:371445" />
        <display value="Genetic syndromic esophageal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:371861" />
        <display value="Genetic hyperaldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:37202" />
        <display value="Interstitial cystitis" />
      </concept>
      <concept>
        <code value="ORPHA:373" />
        <display value="Simpson-Golabi-Behmel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:374" />
        <display value="Goldenhar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:375" />
        <display value="Anti-glomerular basement membrane disease" />
      </concept>
      <concept>
        <code value="ORPHA:37553" />
        <display value="Cardiodysrhythmic potassium-sensitive periodic paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:37559" />
        <display value="Acquired kinky hair syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:376" />
        <display value="Gordon syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:37612" />
        <display value="Episodic ataxia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:376724" />
        <display value="Generalized isolated dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:377" />
        <display value="Gorlin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:37748" />
        <display value="Schnitzler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:379" />
        <display value="Chronic granulomatous disease" />
      </concept>
      <concept>
        <code value="ORPHA:38" />
        <display value="Acrokeratoelastoidosis of Costa" />
      </concept>
      <concept>
        <code value="ORPHA:380" />
        <display value="Greig cephalopolysyndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:381" />
        <display value="Griscelli syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:382" />
        <display value="Guanidinoacetate methyltransferase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:383" />
        <display value="X-linked mixed deafness with perilymphatic gusher" />
      </concept>
      <concept>
        <code value="ORPHA:384" />
        <display value="Palmoplantar keratoderma-sclerodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:385" />
        <display value="Neurodegeneration with brain iron accumulation" />
      </concept>
      <concept>
        <code value="ORPHA:386" />
        <display value="Hepatic cystic hamartoma" />
      </concept>
      <concept>
        <code value="ORPHA:388" />
        <display value="Hirschsprung disease" />
      </concept>
      <concept>
        <code value="ORPHA:38874" />
        <display value="Dihydropyrimidinuria" />
      </concept>
      <concept>
        <code value="ORPHA:389" />
        <display value="Langerhans cell histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:39" />
        <display value="Acromelanosis" />
      </concept>
      <concept>
        <code value="ORPHA:390" />
        <display value="Histoplasmosis" />
      </concept>
      <concept>
        <code value="ORPHA:39041" />
        <display value="Omenn syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:39044" />
        <display value="Uveal melanoma" />
      </concept>
      <concept>
        <code value="ORPHA:391" />
        <display value="Classic Hodgkin lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:391307" />
        <display value="Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391311" />
        <display value="Susceptibility to viral and mycobacterial infections" />
      </concept>
      <concept>
        <code value="ORPHA:391316" />
        <display value="Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression" />
      </concept>
      <concept>
        <code value="ORPHA:391320" />
        <display value="East Texas bleeding disorder" />
      </concept>
      <concept>
        <code value="ORPHA:391327" />
        <display value="X-linked calvarial hyperostosis" />
      </concept>
      <concept>
        <code value="ORPHA:391330" />
        <display value="X-linked osteoporosis with fractures" />
      </concept>
      <concept>
        <code value="ORPHA:391343" />
        <display value="Fatal post-viral neurodegenerative disorder" />
      </concept>
      <concept>
        <code value="ORPHA:391348" />
        <display value="Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391351" />
        <display value="SURF1-related Charcot-Marie-Tooth disease type 4" />
      </concept>
      <concept>
        <code value="ORPHA:391366" />
        <display value="Growth retardation-mild developmental delay-chronic hepatitis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391372" />
        <display value="Intellectual disability-severe speech delay-mild dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391376" />
        <display value="Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391381" />
        <display value="Disorder of asparagine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:391384" />
        <display value="Familial episodic pain syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391389" />
        <display value="Familial episodic pain syndrome with predominantly upper body involvement" />
      </concept>
      <concept>
        <code value="ORPHA:391392" />
        <display value="Familial episodic pain syndrome with predominantly lower limb involvement" />
      </concept>
      <concept>
        <code value="ORPHA:391397" />
        <display value="Hereditary sensory and autonomic neuropathy type 7" />
      </concept>
      <concept>
        <code value="ORPHA:391408" />
        <display value="Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391411" />
        <display value="Atypical juvenile parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:391417" />
        <display value="HSD10 disease" />
      </concept>
      <concept>
        <code value="ORPHA:391428" />
        <display value="HSD10 disease, infantile type" />
      </concept>
      <concept>
        <code value="ORPHA:391457" />
        <display value="HSD10 disease, neonatal type" />
      </concept>
      <concept>
        <code value="ORPHA:391474" />
        <display value="Frontorhiny" />
      </concept>
      <concept>
        <code value="ORPHA:391487" />
        <display value="Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391490" />
        <display value="Adult-onset myasthenia gravis" />
      </concept>
      <concept>
        <code value="ORPHA:391497" />
        <display value="Juvenile myasthenia gravis" />
      </concept>
      <concept>
        <code value="ORPHA:391504" />
        <display value="Transient neonatal myasthenia gravis" />
      </concept>
      <concept>
        <code value="ORPHA:391641" />
        <display value="Feingold syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:391646" />
        <display value="Feingold syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:391651" />
        <display value="Glomus tumor" />
      </concept>
      <concept>
        <code value="ORPHA:391665" />
        <display value="Homozygous familial hypercholesterolemia" />
      </concept>
      <concept>
        <code value="ORPHA:391677" />
        <display value="Short stature-optic atrophy-Pelger-Huet anomaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:391711" />
        <display value="Persistent combined dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:391723" />
        <display value="Mucinous adenocarcinoma of the appendix" />
      </concept>
      <concept>
        <code value="ORPHA:391799" />
        <display value="Rare genetic dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:392" />
        <display value="Holt-Oram syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:393" />
        <display value="46,XX testicular disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:394" />
        <display value="Classic homocystinuria" />
      </concept>
      <concept>
        <code value="ORPHA:394529" />
        <display value="Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type" />
      </concept>
      <concept>
        <code value="ORPHA:394532" />
        <display value="Multiple acyl-CoA dehydrogenase deficiency, mild type" />
      </concept>
      <concept>
        <code value="ORPHA:395" />
        <display value="Homocystinuria due to methylene tetrahydrofolate reductase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:396" />
        <display value="Chronic hiccup" />
      </concept>
      <concept>
        <code value="ORPHA:397" />
        <display value="Giant cell arteritis" />
      </concept>
      <concept>
        <code value="ORPHA:397587" />
        <display value="Deep dermatophytosis" />
      </concept>
      <concept>
        <code value="ORPHA:397590" />
        <display value="Silver-Russell syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:397593" />
        <display value="Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:397596" />
        <display value="Activated PI3K-delta syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397606" />
        <display value="PrP systemic amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:397612" />
        <display value="Macrocephaly-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397615" />
        <display value="Obesity due to CEP19 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:397618" />
        <display value="Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397623" />
        <display value="Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397685" />
        <display value="Familial  hyperprolactinemia" />
      </concept>
      <concept>
        <code value="ORPHA:397692" />
        <display value="Hereditary isolated aplastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:397695" />
        <display value="3q27.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397709" />
        <display value="Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397715" />
        <display value="Joubert syndrome with Jeune asphyxiating thoracic dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:397725" />
        <display value="COASY protein-associated neurodegeneration" />
      </concept>
      <concept>
        <code value="ORPHA:397735" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2U" />
      </concept>
      <concept>
        <code value="ORPHA:397744" />
        <display value="Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397750" />
        <display value="Periodic paralysis with later-onset distal motor neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:397755" />
        <display value="Periodic paralysis with transient compartment-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397758" />
        <display value="Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:397787" />
        <display value="Severe combined immunodeficiency due to IKK2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:397802" />
        <display value="T+ B+ severe combined immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:397922" />
        <display value="Ferro-cerebro-cutaneous syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397927" />
        <display value="Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397933" />
        <display value="Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397937" />
        <display value="Polyglucosan body myopathy type 1" />
      </concept>
      <concept>
        <code value="ORPHA:397941" />
        <display value="MAN1B1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:397946" />
        <display value="Autosomal recessive spastic paraplegia type 58" />
      </concept>
      <concept>
        <code value="ORPHA:397951" />
        <display value="Microcephaly-thin corpus callosum-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:397959" />
        <display value="TCR-alpha-beta-positive T-cell deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:397964" />
        <display value="Combined immunodeficiency due to MALT1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:397968" />
        <display value="Charcot-Marie-Tooth disease type 2R" />
      </concept>
      <concept>
        <code value="ORPHA:397973" />
        <display value="Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:398043" />
        <display value="Malignant tumor of penis" />
      </concept>
      <concept>
        <code value="ORPHA:398053" />
        <display value="Adenocarcinoma of the penis" />
      </concept>
      <concept>
        <code value="ORPHA:398058" />
        <display value="Squamous cell carcinoma of the penis" />
      </concept>
      <concept>
        <code value="ORPHA:398063" />
        <display value="Refractory celiac disease" />
      </concept>
      <concept>
        <code value="ORPHA:398069" />
        <display value="Prader-Willi syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:398073" />
        <display value="Prader-Willi-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:398079" />
        <display value="Prader-Willi-like syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:398088" />
        <display value="Hereditary cryohydrocytosis with normal stomatin" />
      </concept>
      <concept>
        <code value="ORPHA:398091" />
        <display value="Secondary neonatal autoimmune disease" />
      </concept>
      <concept>
        <code value="ORPHA:398097" />
        <display value="Neonatal antiphospholipid syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:398109" />
        <display value="Neonatal autoimmune hemolytic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:398117" />
        <display value="Neonatal dermatomyositis" />
      </concept>
      <concept>
        <code value="ORPHA:39812" />
        <display value="Graft versus host disease" />
      </concept>
      <concept>
        <code value="ORPHA:398124" />
        <display value="Neonatal lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:398127" />
        <display value="Neonatal scleroderma" />
      </concept>
      <concept>
        <code value="ORPHA:398147" />
        <display value="Persistent idiopathic facial pain" />
      </concept>
      <concept>
        <code value="ORPHA:398156" />
        <display value="Oculoauriculofrontonasal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:398166" />
        <display value="Focal facial dermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:398173" />
        <display value="Focal facial dermal dysplasia type II" />
      </concept>
      <concept>
        <code value="ORPHA:398189" />
        <display value="Focal facial dermal dysplasia type IV" />
      </concept>
      <concept>
        <code value="ORPHA:398934" />
        <display value="Malignant epithelial tumor of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:398940" />
        <display value="Malignant non-epithelial tumor of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:398961" />
        <display value="Mucinous adenocarcinoma of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:398971" />
        <display value="Clear cell adenocarcinoma of the ovary" />
      </concept>
      <concept>
        <code value="ORPHA:398980" />
        <display value="Primary peritoneal serous/papillary carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:398987" />
        <display value="Malignant teratoma of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:399" />
        <display value="Huntington disease" />
      </concept>
      <concept>
        <code value="ORPHA:399058" />
        <display value="Alpha-B crystallin-related late-onset distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:399081" />
        <display value="KLHL9-related early-onset distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:399086" />
        <display value="Finnish upper limb-onset distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:399096" />
        <display value="Distal anoctaminopathy" />
      </concept>
      <concept>
        <code value="ORPHA:399103" />
        <display value="Distal nebulin myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:399158" />
        <display value="Osteonecrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399164" />
        <display value="Avascular necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399169" />
        <display value="Secondary avascular necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399175" />
        <display value="Traumatic avascular necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399180" />
        <display value="Secondary non-traumatic avascular necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399185" />
        <display value="Rare hereditary disease with avascular necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399293" />
        <display value="Osteonecrosis of the jaw" />
      </concept>
      <concept>
        <code value="ORPHA:399302" />
        <display value="Primary avascular necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399307" />
        <display value="Idiopathic avascular necrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399319" />
        <display value="Osteochondrosis" />
      </concept>
      <concept>
        <code value="ORPHA:399329" />
        <display value="Epiphysiolysis of the hip" />
      </concept>
      <concept>
        <code value="ORPHA:399380" />
        <display value="Osteonecrosis of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:399388" />
        <display value="Avascular necrosis of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:399391" />
        <display value="Osteochondrosis of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:399572" />
        <display value="Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399584" />
        <display value="Rare male infertility due to adrenal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399685" />
        <display value="Rare male infertility due to testicular endocrine disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399764" />
        <display value="Male infertility due to gonadal dysgenesis or sperm disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399771" />
        <display value="Male infertility due to sperm disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399775" />
        <display value="Male infertility with spermatogenesis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399786" />
        <display value="Male infertility with spermatogenesis disorder due to single gene mutation" />
      </concept>
      <concept>
        <code value="ORPHA:399805" />
        <display value="Male infertility with azoospermia or oligozoospermia due to single gene mutation" />
      </concept>
      <concept>
        <code value="ORPHA:399808" />
        <display value="Male infertility with teratozoospermia due to single gene mutation" />
      </concept>
      <concept>
        <code value="ORPHA:399813" />
        <display value="Male infertility due to sperm motility disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399824" />
        <display value="Rare disorder with obstructive azoospermia" />
      </concept>
      <concept>
        <code value="ORPHA:399831" />
        <display value="Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399839" />
        <display value="Rare female infertility due to a congenital hypogonadotropic hypogonadism" />
      </concept>
      <concept>
        <code value="ORPHA:399846" />
        <display value="Rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism" />
      </concept>
      <concept>
        <code value="ORPHA:399849" />
        <display value="Rare female infertility due to an adrenal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:399853" />
        <display value="Rare female infertility due to an anomaly of ovarian function" />
      </concept>
      <concept>
        <code value="ORPHA:399877" />
        <display value="Rare female infertility due to gonadal dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:399882" />
        <display value="Rare female infertility due to an implantation defect" />
      </concept>
      <concept>
        <code value="ORPHA:399980" />
        <display value="Rare genetic male infertility" />
      </concept>
      <concept>
        <code value="ORPHA:399983" />
        <display value="Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:399994" />
        <display value="Rare male infertility due to adrenal disorder of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:399998" />
        <display value="Male infertility due to obstructive azoospermia of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:40" />
        <display value="Acromesomelic dysplasia, Maroteaux type" />
      </concept>
      <concept>
        <code value="ORPHA:400" />
        <display value="Cystic echinococcosis" />
      </concept>
      <concept>
        <code value="ORPHA:400003" />
        <display value="Rare genetic disorder with obstructive azoospermia" />
      </concept>
      <concept>
        <code value="ORPHA:400008" />
        <display value="Rare genetic female infertility" />
      </concept>
      <concept>
        <code value="ORPHA:400011" />
        <display value="Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:400018" />
        <display value="Rare female infertility due to adrenal disorder of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:400022" />
        <display value="Rare female infertility due to an anomaly of ovarian function of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:400025" />
        <display value="Female infertility due to an implantation defect of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:401" />
        <display value="Hymenolepiasis" />
      </concept>
      <concept>
        <code value="ORPHA:401764" />
        <display value="Pancytopenia-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:401768" />
        <display value="Proximal myopathy with extrapyramidal signs" />
      </concept>
      <concept>
        <code value="ORPHA:401777" />
        <display value="Optic atrophy-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:401780" />
        <display value="Autosomal recessive spastic paraplegia type 61" />
      </concept>
      <concept>
        <code value="ORPHA:401785" />
        <display value="Autosomal recessive spastic paraplegia type 62" />
      </concept>
      <concept>
        <code value="ORPHA:401795" />
        <display value="Autosomal recessive spastic paraplegia type 59" />
      </concept>
      <concept>
        <code value="ORPHA:401800" />
        <display value="Autosomal recessive spastic paraplegia type 60" />
      </concept>
      <concept>
        <code value="ORPHA:401805" />
        <display value="Autosomal recessive spastic paraplegia type 63" />
      </concept>
      <concept>
        <code value="ORPHA:401810" />
        <display value="Autosomal recessive spastic paraplegia type 64" />
      </concept>
      <concept>
        <code value="ORPHA:401815" />
        <display value="Autosomal recessive spastic paraplegia type 66" />
      </concept>
      <concept>
        <code value="ORPHA:401820" />
        <display value="Autosomal recessive spastic paraplegia type 67" />
      </concept>
      <concept>
        <code value="ORPHA:401830" />
        <display value="Autosomal recessive spastic paraplegia type 69" />
      </concept>
      <concept>
        <code value="ORPHA:401835" />
        <display value="Autosomal recessive spastic paraplegia type 70" />
      </concept>
      <concept>
        <code value="ORPHA:401840" />
        <display value="Autosomal recessive spastic paraplegia type 71" />
      </concept>
      <concept>
        <code value="ORPHA:401849" />
        <display value="Autosomal spastic paraplegia type 72" />
      </concept>
      <concept>
        <code value="ORPHA:401854" />
        <display value="Lipoic acid biosynthesis defect" />
      </concept>
      <concept>
        <code value="ORPHA:401859" />
        <display value="Lipoic acid synthetase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:401862" />
        <display value="Lipoyl transferase 1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:401866" />
        <display value="Childhood-onset spasticity with hyperglycinemia" />
      </concept>
      <concept>
        <code value="ORPHA:401869" />
        <display value="Multiple mitochondrial dysfunctions syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:401874" />
        <display value="Multiple mitochondrial dysfunctions syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:401901" />
        <display value="Huntington disease-like syndrome due to C9ORF72 expansions" />
      </concept>
      <concept>
        <code value="ORPHA:401911" />
        <display value="AXIN2-related attenuated familial adenomatous polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:401920" />
        <display value="Fibrolamellar hepatocellular carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:401923" />
        <display value="9q31.1q31.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:401935" />
        <display value="14q24.1q24.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:401942" />
        <display value="Familial median cleft of the upper and lower lips" />
      </concept>
      <concept>
        <code value="ORPHA:401945" />
        <display value="Moyamoya disease with early-onset achalasia" />
      </concept>
      <concept>
        <code value="ORPHA:401948" />
        <display value="Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:401953" />
        <display value="Episodic ataxia with slurred speech" />
      </concept>
      <concept>
        <code value="ORPHA:401959" />
        <display value="Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:401964" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons" />
      </concept>
      <concept>
        <code value="ORPHA:401973" />
        <display value="MEND syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:401979" />
        <display value="Autosomal recessive spondylometaphyseal dysplasia, Megarbane type" />
      </concept>
      <concept>
        <code value="ORPHA:401986" />
        <display value="1p31p32 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:401993" />
        <display value="Cold-induced sweating syndrome-hyperthermia spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:401996" />
        <display value="Karyomegalic interstitial nephritis" />
      </concept>
      <concept>
        <code value="ORPHA:402003" />
        <display value="Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering" />
      </concept>
      <concept>
        <code value="ORPHA:402007" />
        <display value="Lichen myxedematosus" />
      </concept>
      <concept>
        <code value="ORPHA:402014" />
        <display value="Acute myeloid leukemia with t(6;9)(p23;q34)" />
      </concept>
      <concept>
        <code value="ORPHA:402017" />
        <display value="Acute myeloid leukemia with t(9;11)(p22;q23)" />
      </concept>
      <concept>
        <code value="ORPHA:402020" />
        <display value="Acute myeloid leukemia with inv3(q21;q26.2) or t(3;3)(q21;q26.2)" />
      </concept>
      <concept>
        <code value="ORPHA:402023" />
        <display value="Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)" />
      </concept>
      <concept>
        <code value="ORPHA:402026" />
        <display value="Acute myeloid leukemia with NPM1 somatic mutations" />
      </concept>
      <concept>
        <code value="ORPHA:402029" />
        <display value="Primary eosinophilic gastrointestinal disease" />
      </concept>
      <concept>
        <code value="ORPHA:402035" />
        <display value="Eosinophilic colitis" />
      </concept>
      <concept>
        <code value="ORPHA:402041" />
        <display value="Autosomal recessive distal renal tubular acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:402075" />
        <display value="Familial bicuspid aortic valve" />
      </concept>
      <concept>
        <code value="ORPHA:402082" />
        <display value="Progressive myoclonic epilepsy type 5" />
      </concept>
      <concept>
        <code value="ORPHA:402364" />
        <display value="Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly" />
      </concept>
      <concept>
        <code value="ORPHA:402823" />
        <display value="Hepatitis delta" />
      </concept>
      <concept>
        <code value="ORPHA:403" />
        <display value="Familial hyperaldosteronism type I" />
      </concept>
      <concept>
        <code value="ORPHA:40366" />
        <display value="Acitretin/etretinate embryopathy" />
      </concept>
      <concept>
        <code value="ORPHA:404" />
        <display value="Familial hyperaldosteronism type II" />
      </concept>
      <concept>
        <code value="ORPHA:404437" />
        <display value="Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404440" />
        <display value="Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:404443" />
        <display value="Tall stature-intellectual disability-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404448" />
        <display value="ADNP syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404451" />
        <display value="FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404454" />
        <display value="Alacrimia-choreoathetosis-liver dysfunction syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404463" />
        <display value="Multisystemic smooth muscle dysfunction syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404466" />
        <display value="Female infertility due to zona pellucida defect" />
      </concept>
      <concept>
        <code value="ORPHA:404469" />
        <display value="Rare female infertility due to oocyte maturation defect" />
      </concept>
      <concept>
        <code value="ORPHA:404473" />
        <display value="Severe intellectual disability-progressive spastic diplegia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404476" />
        <display value="Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404481" />
        <display value="Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404493" />
        <display value="Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:404499" />
        <display value="Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:404507" />
        <display value="Chondromyxoid fibroma" />
      </concept>
      <concept>
        <code value="ORPHA:404511" />
        <display value="Clear cell papillary renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:404514" />
        <display value="Acquired cystic disease-associated renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:404521" />
        <display value="Spinal muscular atrophy with respiratory distress type 2" />
      </concept>
      <concept>
        <code value="ORPHA:404538" />
        <display value="X-linked distal hereditary motor neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:404546" />
        <display value="DITRA" />
      </concept>
      <concept>
        <code value="ORPHA:404553" />
        <display value="Vasculitis due to ADA2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:404560" />
        <display value="Familial atypical multiple mole melanoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:404568" />
        <display value="Dysostosis of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:404571" />
        <display value="Dysostosis of genetic origin with limb anomaly as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:404574" />
        <display value="Genetic syndrome with limb reduction defects" />
      </concept>
      <concept>
        <code value="ORPHA:404577" />
        <display value="Genetic syndrome with limb malformations as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:404580" />
        <display value="Polyarticular juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:404584" />
        <display value="Rare genetic bone development disorder" />
      </concept>
      <concept>
        <code value="ORPHA:405" />
        <display value="Familial hypocalciuric hypercalcemia" />
      </concept>
      <concept>
        <code value="ORPHA:407" />
        <display value="Glycine encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:408" />
        <display value="Isolated glycerol kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:409" />
        <display value="Hyperkeratosis lenticularis perstans" />
      </concept>
      <concept>
        <code value="ORPHA:40923" />
        <display value="Eales disease" />
      </concept>
      <concept>
        <code value="ORPHA:41" />
        <display value="Dyschromatosis symmetrica hereditaria" />
      </concept>
      <concept>
        <code value="ORPHA:411493" />
        <display value="Pontocerebellar hypoplasia type 10" />
      </concept>
      <concept>
        <code value="ORPHA:411501" />
        <display value="Williams-Campbell syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:411511" />
        <display value="Angelman syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:411515" />
        <display value="Angelman syndrome due to imprinting defect in 15q11-q13" />
      </concept>
      <concept>
        <code value="ORPHA:411536" />
        <display value="Mild phosphoribosylpyrophosphate synthetase superactivity" />
      </concept>
      <concept>
        <code value="ORPHA:411543" />
        <display value="Severe phosphoribosylpyrophosphate synthetase superactivity" />
      </concept>
      <concept>
        <code value="ORPHA:411590" />
        <display value="Wolfram-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:411593" />
        <display value="Insulin autoimmune syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:411602" />
        <display value="Hereditary late-onset Parkinson disease" />
      </concept>
      <concept>
        <code value="ORPHA:411629" />
        <display value="Nephropathic infantile cystinosis" />
      </concept>
      <concept>
        <code value="ORPHA:411634" />
        <display value="Juvenile nephropathic cystinosis" />
      </concept>
      <concept>
        <code value="ORPHA:411641" />
        <display value="Ocular cystinosis" />
      </concept>
      <concept>
        <code value="ORPHA:411696" />
        <display value="Proton-pump inhibitor-responsive esophageal eosinophilia" />
      </concept>
      <concept>
        <code value="ORPHA:411703" />
        <display value="Pulmonary non-tuberculous mycobacterial infection" />
      </concept>
      <concept>
        <code value="ORPHA:411709" />
        <display value="Renal agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:411712" />
        <display value="Maternal riboflavin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:411777" />
        <display value="Generalized eruptive keratoacanthoma" />
      </concept>
      <concept>
        <code value="ORPHA:411788" />
        <display value="Familial isolated trichomegaly" />
      </concept>
      <concept>
        <code value="ORPHA:411986" />
        <display value="Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:412" />
        <display value="Hyperlipoproteinemia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:412022" />
        <display value="Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:412035" />
        <display value="13q12.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:412057" />
        <display value="Autosomal recessive cerebellar ataxia due to STUB1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:412066" />
        <display value="PRKAR1B-related neurodegenerative dementia with intermediate filaments" />
      </concept>
      <concept>
        <code value="ORPHA:412069" />
        <display value="AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:412181" />
        <display value="Epidermolysis bullosa simplex due to BP230 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:412189" />
        <display value="Epidermolysis bullosa simplex due to exophilin 5 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:412206" />
        <display value="Primary failure of tooth eruption" />
      </concept>
      <concept>
        <code value="ORPHA:412217" />
        <display value="Dystonia-aphonia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:414" />
        <display value="Gyrate atrophy of choroid and retina" />
      </concept>
      <concept>
        <code value="ORPHA:414726" />
        <display value="Genetic facial cleft" />
      </concept>
      <concept>
        <code value="ORPHA:415" />
        <display value="Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:415286" />
        <display value="Kernicterus spectrum disorder" />
      </concept>
      <concept>
        <code value="ORPHA:416" />
        <display value="Primary hyperoxaluria" />
      </concept>
      <concept>
        <code value="ORPHA:417" />
        <display value="Neonatal severe primary hyperparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:41751" />
        <display value="Bietti crystalline dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:418" />
        <display value="Congenital adrenal hyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:418945" />
        <display value="Carcinoma of esophagus, salivary gland type" />
      </concept>
      <concept>
        <code value="ORPHA:418951" />
        <display value="Undifferentiated carcinoma of esophagus" />
      </concept>
      <concept>
        <code value="ORPHA:418959" />
        <display value="Squamous cell carcinoma of the stomach" />
      </concept>
      <concept>
        <code value="ORPHA:419" />
        <display value="Hyperprolinemia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:42" />
        <display value="Medium chain acyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:420179" />
        <display value="Malan overgrowth syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:420259" />
        <display value="Secondary pulmonary alveolar proteinosis" />
      </concept>
      <concept>
        <code value="ORPHA:420402" />
        <display value="Semicircular canal dehiscence syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:420429" />
        <display value="Glycogen storage disease due to acid maltase deficiency, late-onset" />
      </concept>
      <concept>
        <code value="ORPHA:420485" />
        <display value="Cranio-cervical dystonia with laryngeal and upper-limb involvement" />
      </concept>
      <concept>
        <code value="ORPHA:420492" />
        <display value="Adult-onset cervical dystonia, DYT23 type" />
      </concept>
      <concept>
        <code value="ORPHA:420556" />
        <display value="Visual snow syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:420561" />
        <display value="Temple-Baraitser syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:420566" />
        <display value="Bleeding disorder due to CalDAG-GEFI deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:420573" />
        <display value="Severe combined immunodeficiency due to CTPS1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:420584" />
        <display value="Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:420611" />
        <display value="Transient myeloproliferative syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:42062" />
        <display value="Iminoglycinuria" />
      </concept>
      <concept>
        <code value="ORPHA:420686" />
        <display value="Woolly hair-palmoplantar keratoderma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:420699" />
        <display value="Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:420702" />
        <display value="Autosomal recessive severe congenital neutropenia due to CSF3R deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:420728" />
        <display value="Combined oxidative phosphorylation defect type 20" />
      </concept>
      <concept>
        <code value="ORPHA:420733" />
        <display value="Combined oxidative phosphorylation defect type 21" />
      </concept>
      <concept>
        <code value="ORPHA:420741" />
        <display value="RIDDLE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:420755" />
        <display value="Rare genetic odontal or periodontal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:420789" />
        <display value="Autoimmune encephalopathy with parasomnia and obstructive sleep apnea" />
      </concept>
      <concept>
        <code value="ORPHA:420794" />
        <display value="Cono-spondylar dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:422" />
        <display value="Idiopathic and/or familial pulmonary arterial hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:422519" />
        <display value="3-Phosphoglycerate dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:422526" />
        <display value="Hereditary clear cell renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:423" />
        <display value="Malignant hyperthermia of anesthesia" />
      </concept>
      <concept>
        <code value="ORPHA:423275" />
        <display value="Spinocerebellar ataxia type 40" />
      </concept>
      <concept>
        <code value="ORPHA:423296" />
        <display value="Spinocerebellar ataxia type 38" />
      </concept>
      <concept>
        <code value="ORPHA:423306" />
        <display value="Microcephaly-short stature-intellectual disability-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:423384" />
        <display value="Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:423454" />
        <display value="Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:423461" />
        <display value="Mucolipidosis type III alpha/beta" />
      </concept>
      <concept>
        <code value="ORPHA:423470" />
        <display value="Mucolipidosis type III gamma" />
      </concept>
      <concept>
        <code value="ORPHA:423479" />
        <display value="X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:423655" />
        <display value="ARX-related encephalopathy-brain malformation spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:423662" />
        <display value="Rare autonomic nervous system disorder" />
      </concept>
      <concept>
        <code value="ORPHA:423693" />
        <display value="Double outlet right ventricle with subaortic or doubly committed ventricular septal defect" />
      </concept>
      <concept>
        <code value="ORPHA:423712" />
        <display value="Double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy" />
      </concept>
      <concept>
        <code value="ORPHA:423717" />
        <display value="Cutaneous larva migrans" />
      </concept>
      <concept>
        <code value="ORPHA:423771" />
        <display value="Rare carcinoma of stomach" />
      </concept>
      <concept>
        <code value="ORPHA:423776" />
        <display value="Hereditary gastric cancer" />
      </concept>
      <concept>
        <code value="ORPHA:423781" />
        <display value="Carcinoma of stomach, salivary gland type" />
      </concept>
      <concept>
        <code value="ORPHA:423786" />
        <display value="Undifferentiated carcinoma of stomach" />
      </concept>
      <concept>
        <code value="ORPHA:423793" />
        <display value="Rare tumor of small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:423798" />
        <display value="Mesenchymal tumor of small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:423894" />
        <display value="Microcephaly-complex motor and sensory axonal neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:423957" />
        <display value="Rare carcinoma of small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:423968" />
        <display value="Squamous cell carcinoma of the small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:423975" />
        <display value="Neuroendocrine tumor of the small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:423982" />
        <display value="Epithelial tumor of the appendix" />
      </concept>
      <concept>
        <code value="ORPHA:423991" />
        <display value="Rare epithelial tumor of colon" />
      </concept>
      <concept>
        <code value="ORPHA:423994" />
        <display value="Squamous cell carcinoma of the colon" />
      </concept>
      <concept>
        <code value="ORPHA:423998" />
        <display value="Rare epithelial tumor of rectum" />
      </concept>
      <concept>
        <code value="ORPHA:424" />
        <display value="Familial hyperthyroidism due to mutations in TSH receptor" />
      </concept>
      <concept>
        <code value="ORPHA:424002" />
        <display value="Squamous cell carcinoma of the rectum" />
      </concept>
      <concept>
        <code value="ORPHA:424010" />
        <display value="Epithelial tumor of anal canal" />
      </concept>
      <concept>
        <code value="ORPHA:424013" />
        <display value="Carcinoma of the anal canal" />
      </concept>
      <concept>
        <code value="ORPHA:424016" />
        <display value="Adenocarcinoma of the anal canal" />
      </concept>
      <concept>
        <code value="ORPHA:424019" />
        <display value="Squamous cell carcinoma of the anal canal" />
      </concept>
      <concept>
        <code value="ORPHA:424027" />
        <display value="Progressive myoclonic epilepsy type 8" />
      </concept>
      <concept>
        <code value="ORPHA:424033" />
        <display value="Rare epithelial tumor of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:424039" />
        <display value="Squamous cell carcinoma of the pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:424046" />
        <display value="Acinar cell carcinoma of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:424053" />
        <display value="Mucinous cystadenocarcinoma of the pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:424058" />
        <display value="Intraductal papillary mucinous carcinoma of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:424065" />
        <display value="Solid pseudopapillary carcinoma of the pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:424073" />
        <display value="Serous cystadenocarcinoma of the pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:424080" />
        <display value="Osteoclastic giant cell tumor of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:424099" />
        <display value="Colobomatous microphthalmia-rhizomelic dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:424107" />
        <display value="Congenital myopathy with myasthenic-like onset" />
      </concept>
      <concept>
        <code value="ORPHA:424261" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2Y" />
      </concept>
      <concept>
        <code value="ORPHA:424925" />
        <display value="Qualitative or quantitative defects of Torsin-1A-interacting protein 1" />
      </concept>
      <concept>
        <code value="ORPHA:424933" />
        <display value="Rare epithelial tumor of liver and intrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:424936" />
        <display value="Carcinoma of liver and intrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:424943" />
        <display value="Adenocarcinoma of the liver and intrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:424970" />
        <display value="Undifferentiated carcinoma of liver and intrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:424975" />
        <display value="Squamous cell carcinoma of liver and intrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:424982" />
        <display value="Biliary cystadenocarcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:424991" />
        <display value="Adenocarcinoma of the gallbladder and extrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:424996" />
        <display value="Squamous cell carcinoma of gallbladder and extrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:425" />
        <display value="Apolipoprotein A-I deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:425003" />
        <display value="Inherited digestive cancer-predisposing syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:425120" />
        <display value="STING-associated vasculopathy with onset in infancy" />
      </concept>
      <concept>
        <code value="ORPHA:425368" />
        <display value="Rare epithelial tumor of small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:42642" />
        <display value="PFAPA syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:42665" />
        <display value="Tietz syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:427" />
        <display value="Familial hypoaldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:42738" />
        <display value="Severe congenital neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:42775" />
        <display value="PHACE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:428" />
        <display value="Autosomal dominant hypocalcemia" />
      </concept>
      <concept>
        <code value="ORPHA:429" />
        <display value="Hypochondroplasia" />
      </concept>
      <concept>
        <code value="ORPHA:43" />
        <display value="X-linked adrenoleukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:431140" />
        <display value="X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:431149" />
        <display value="Combined immunodeficiency due to OX40 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:43115" />
        <display value="Hereditary myopathy with lactic acidosis due to ISCU deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:431156" />
        <display value="Primary immunodeficiency with predisposition to severe viral infection" />
      </concept>
      <concept>
        <code value="ORPHA:43116" />
        <display value="Serotonin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:431166" />
        <display value="Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection" />
      </concept>
      <concept>
        <code value="ORPHA:43117" />
        <display value="Acute tricyclic antidepressant poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:43119" />
        <display value="Acute poisoning by drugs with membrane-stabilizing effect" />
      </concept>
      <concept>
        <code value="ORPHA:431255" />
        <display value="Scapuloperoneal spinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:431263" />
        <display value="Late-onset scapuloperoneal muscular dystrophy with hyaline bodies" />
      </concept>
      <concept>
        <code value="ORPHA:431272" />
        <display value="X-linked scapuloperoneal muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:431320" />
        <display value="Spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder" />
      </concept>
      <concept>
        <code value="ORPHA:431329" />
        <display value="Autosomal recessive spastic paraplegia type 57" />
      </concept>
      <concept>
        <code value="ORPHA:431341" />
        <display value="Patent urachus" />
      </concept>
      <concept>
        <code value="ORPHA:431344" />
        <display value="Urachal sinus" />
      </concept>
      <concept>
        <code value="ORPHA:431347" />
        <display value="Urachal diverticulum" />
      </concept>
      <concept>
        <code value="ORPHA:431353" />
        <display value="Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:431361" />
        <display value="Progressive encephalopathy with leukodystrophy due to DECR deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:432" />
        <display value="Normosmic congenital hypogonadotropic hypogonadism" />
      </concept>
      <concept>
        <code value="ORPHA:43393" />
        <display value="Lambert-Eaton myasthenic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:434179" />
        <display value="Orofaciodigital syndrome type 14" />
      </concept>
      <concept>
        <code value="ORPHA:434786" />
        <display value="Rare genetic autonomic nervous system disorder" />
      </concept>
      <concept>
        <code value="ORPHA:434809" />
        <display value="Syndrome with woolly hair" />
      </concept>
      <concept>
        <code value="ORPHA:435" />
        <display value="Ito hypomelanosis" />
      </concept>
      <concept>
        <code value="ORPHA:435329" />
        <display value="Familial ossifying fibroma" />
      </concept>
      <concept>
        <code value="ORPHA:435365" />
        <display value="Fetal lower urinary tract obstruction" />
      </concept>
      <concept>
        <code value="ORPHA:435372" />
        <display value="Anterior urethral valve" />
      </concept>
      <concept>
        <code value="ORPHA:435387" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2Y" />
      </concept>
      <concept>
        <code value="ORPHA:435438" />
        <display value="Progressive myoclonic epilepsy type 7" />
      </concept>
      <concept>
        <code value="ORPHA:435554" />
        <display value="Genetic precocious puberty" />
      </concept>
      <concept>
        <code value="ORPHA:435561" />
        <display value="Precocious puberty in female" />
      </concept>
      <concept>
        <code value="ORPHA:435564" />
        <display value="Genetic precocious puberty in female" />
      </concept>
      <concept>
        <code value="ORPHA:435603" />
        <display value="Genetic otorhinolaryngological malformation" />
      </concept>
      <concept>
        <code value="ORPHA:435606" />
        <display value="Genetic nose and cavum anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:435609" />
        <display value="Genetic larynx anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:435612" />
        <display value="Genetic tracheal anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:435628" />
        <display value="Keppen-Lubinsky syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:435638" />
        <display value="3p25.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:435651" />
        <display value="CIDEC-related familial partial lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:435660" />
        <display value="LIPE-related familial partial lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:435743" />
        <display value="Congenital urachal anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:435804" />
        <display value="Short stature-advanced bone age-early-onset osteoarthritis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:435819" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation" />
      </concept>
      <concept>
        <code value="ORPHA:435845" />
        <display value="Lethal neonatal spasticity-epileptic encephalopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:435930" />
        <display value="Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:435934" />
        <display value="COG2-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:435938" />
        <display value="X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:435953" />
        <display value="Progeroid features-hepatocellular carcinoma predisposition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:435988" />
        <display value="Chronic atrial and intestinal dysrhythmia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:435998" />
        <display value="Autosomal recessive intermediate Charcot-Marie-Tooth disease type D" />
      </concept>
      <concept>
        <code value="ORPHA:436" />
        <display value="Hypophosphatasia" />
      </concept>
      <concept>
        <code value="ORPHA:436003" />
        <display value="Contractures-developmental delay-Pierre Robin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:436141" />
        <display value="Severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:436144" />
        <display value="Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:436151" />
        <display value="Intellectual disability-expressive aphasia-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:436159" />
        <display value="Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency" />
      </concept>
      <concept>
        <code value="ORPHA:436166" />
        <display value="Periodic fever-infantile enterocolitis-autoinflammatory syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:436169" />
        <display value="Thrombomodulin-related bleeding disorder" />
      </concept>
      <concept>
        <code value="ORPHA:436174" />
        <display value="Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:436182" />
        <display value="Microcephalic primordial dwarfism-insulin resistance syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:436242" />
        <display value="Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease" />
      </concept>
      <concept>
        <code value="ORPHA:436245" />
        <display value="Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:436252" />
        <display value="Combined immunodeficiency-enteropathy spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:436271" />
        <display value="Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:436274" />
        <display value="Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa" />
      </concept>
      <concept>
        <code value="ORPHA:437" />
        <display value="Hypophosphatemic rickets" />
      </concept>
      <concept>
        <code value="ORPHA:437552" />
        <display value="Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity" />
      </concept>
      <concept>
        <code value="ORPHA:437572" />
        <display value="MYH7-related late-onset scapuloperoneal muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:438072" />
        <display value="Disorder of keton body transport" />
      </concept>
      <concept>
        <code value="ORPHA:438075" />
        <display value="Ketoacidosis due to monocarboxylate transporter-1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:438114" />
        <display value="RARS-related autosomal recessive hypomyelinating leukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:438117" />
        <display value="Steel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:438134" />
        <display value="PCNA-related progressive neurodegenerative photosensitivity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:438159" />
        <display value="STAT3-related early-onset multisystem autoimmune disease" />
      </concept>
      <concept>
        <code value="ORPHA:438178" />
        <display value="Severe intellectual disability-epilepsy-cataract syndrome due to fatty acyl-CoA reductase 1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:438207" />
        <display value="Severe autosomal recessive macrothrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:438213" />
        <display value="PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:438216" />
        <display value="PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:438266" />
        <display value="Progressive encephalomyelitis with rigidity and myoclonus" />
      </concept>
      <concept>
        <code value="ORPHA:438274" />
        <display value="GCGR-related hyperglucagonemia" />
      </concept>
      <concept>
        <code value="ORPHA:438279" />
        <display value="Human infection by orthopoxvirus" />
      </concept>
      <concept>
        <code value="ORPHA:439" />
        <display value="Isolated right ventricular hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:439167" />
        <display value="Placental insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:439175" />
        <display value="Pediatric arterial ischemic stroke" />
      </concept>
      <concept>
        <code value="ORPHA:439196" />
        <display value="Zinc-responsive necrolytic acral erythema" />
      </concept>
      <concept>
        <code value="ORPHA:439202" />
        <display value="Non-recovering obstetric brachial plexus lesion" />
      </concept>
      <concept>
        <code value="ORPHA:439212" />
        <display value="Early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:439218" />
        <display value="KCNQ2-related epileptic encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:439224" />
        <display value="ALECT2 amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:439232" />
        <display value="AApoAIV amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:439246" />
        <display value="ABeta2M amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:439254" />
        <display value="ITM2B amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:439729" />
        <display value="Cutaneous polyarteritis nodosa" />
      </concept>
      <concept>
        <code value="ORPHA:439737" />
        <display value="Primary polyarteritis nodosa" />
      </concept>
      <concept>
        <code value="ORPHA:439746" />
        <display value="Secondary polyarteritis nodosa" />
      </concept>
      <concept>
        <code value="ORPHA:439755" />
        <display value="Single-organ polyarteritis nodosa" />
      </concept>
      <concept>
        <code value="ORPHA:439762" />
        <display value="Systemic polyarteritis nodosa" />
      </concept>
      <concept>
        <code value="ORPHA:439822" />
        <display value="PDE4D haploinsufficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:439849" />
        <display value="Autosomal recessive severe congenital neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:439854" />
        <display value="Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease" />
      </concept>
      <concept>
        <code value="ORPHA:439881" />
        <display value="Plastic bronchitis" />
      </concept>
      <concept>
        <code value="ORPHA:439897" />
        <display value="Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:44" />
        <display value="Neonatal adrenoleukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:440" />
        <display value="Familial hypospadias" />
      </concept>
      <concept>
        <code value="ORPHA:440221" />
        <display value="Congenital oculomotor nerve palsy" />
      </concept>
      <concept>
        <code value="ORPHA:440233" />
        <display value="Congenital abducens nerve palsy" />
      </concept>
      <concept>
        <code value="ORPHA:440354" />
        <display value="Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:440368" />
        <display value="Necrotizing soft tissue infection" />
      </concept>
      <concept>
        <code value="ORPHA:440392" />
        <display value="Interstitial lung disease due to SP-C deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:440402" />
        <display value="Interstitial lung disease due to ABCA3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:440427" />
        <display value="Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:440437" />
        <display value="Familial colorectal cancer Type X" />
      </concept>
      <concept>
        <code value="ORPHA:440701" />
        <display value="Disorders of pentose/polyol metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:440706" />
        <display value="Ribose-5-P isomerase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:440713" />
        <display value="Isolated sedoheptulokinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:440724" />
        <display value="Extensive peripapillary myelinated nerve fibers" />
      </concept>
      <concept>
        <code value="ORPHA:440727" />
        <display value="Combined hamartoma of the retina and retinal pigment epithelium" />
      </concept>
      <concept>
        <code value="ORPHA:440731" />
        <display value="L-ferritin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:440987" />
        <display value="Isolated agenesis of gallbladder" />
      </concept>
      <concept>
        <code value="ORPHA:441" />
        <display value="Pure autonomic failure" />
      </concept>
      <concept>
        <code value="ORPHA:441434" />
        <display value="Syndromic hereditary optic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:441447" />
        <display value="Early-onset posterior subcapsular cataract" />
      </concept>
      <concept>
        <code value="ORPHA:441452" />
        <display value="Early-onset lamellar cataract" />
      </concept>
      <concept>
        <code value="ORPHA:442" />
        <display value="Congenital hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:442582" />
        <display value="AH amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:442835" />
        <display value="Undetermined early-onset epileptic encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:443057" />
        <display value="Sporadic porphyria cutanea tarda" />
      </concept>
      <concept>
        <code value="ORPHA:443062" />
        <display value="Familial porphyria cutanea tarda" />
      </concept>
      <concept>
        <code value="ORPHA:443070" />
        <display value="Hemicrania continua" />
      </concept>
      <concept>
        <code value="ORPHA:443073" />
        <display value="Charcot-Marie-Tooth disease type 2S" />
      </concept>
      <concept>
        <code value="ORPHA:443079" />
        <display value="Central serous chorioretinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:443084" />
        <display value="Baroreflex failure" />
      </concept>
      <concept>
        <code value="ORPHA:443087" />
        <display value="46,XY disorder of sex development due to testicular 17,20-desmolase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:443090" />
        <display value="46,XY disorder of sexual development due to dihydrotestosterone backdoor pathway biosynthesis defect" />
      </concept>
      <concept>
        <code value="ORPHA:443095" />
        <display value="Hyperinsulinemic hypoglycaemia" />
      </concept>
      <concept>
        <code value="ORPHA:443098" />
        <display value="Hyperostosis cranialis interna" />
      </concept>
      <concept>
        <code value="ORPHA:443101" />
        <display value="Hypothalamic adipsic hypernatraemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:443159" />
        <display value="Lymphoplasmacytic lymphoma without IgM production" />
      </concept>
      <concept>
        <code value="ORPHA:443162" />
        <display value="NDE1-related microhydranencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:443167" />
        <display value="NUT midline carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:443173" />
        <display value="Postpartum psychosis" />
      </concept>
      <concept>
        <code value="ORPHA:443180" />
        <display value="Spontaneous intracranial hypotension" />
      </concept>
      <concept>
        <code value="ORPHA:443192" />
        <display value="Classic stiff person syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:443197" />
        <display value="X-linked erythropoietic protoporphyria" />
      </concept>
      <concept>
        <code value="ORPHA:443227" />
        <display value="Paratyphoid fever" />
      </concept>
      <concept>
        <code value="ORPHA:443236" />
        <display value="Postural orthostatic tachycardia syndrome due to NET deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:443287" />
        <display value="ACTH-independent Cushing syndrome due to rare cortisol-producing adrenal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:443291" />
        <display value="HIV-associated cancer" />
      </concept>
      <concept>
        <code value="ORPHA:443804" />
        <display value="Focal stiff limb syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:443811" />
        <display value="PGM3-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:443909" />
        <display value="Hereditary nonpolyposis colon cancer" />
      </concept>
      <concept>
        <code value="ORPHA:443950" />
        <display value="DNAJB2-related Charcot-Marie-Tooth disease type 2" />
      </concept>
      <concept>
        <code value="ORPHA:443988" />
        <display value="Ventriculomegaly-cystic kidney disease" />
      </concept>
      <concept>
        <code value="ORPHA:443995" />
        <display value="Mandibulofacial dysostosis with alopecia" />
      </concept>
      <concept>
        <code value="ORPHA:444" />
        <display value="Marie Unna hereditary hypotrichosis" />
      </concept>
      <concept>
        <code value="ORPHA:444002" />
        <display value="11q22.2q22.3 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444013" />
        <display value="Combined oxidative phosphorylation defect type 23" />
      </concept>
      <concept>
        <code value="ORPHA:444048" />
        <display value="46,XX ovarian dysgenesis-short stature syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444051" />
        <display value="20q11.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444069" />
        <display value="Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444072" />
        <display value="Cerebellar-facial-dental syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444077" />
        <display value="Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444092" />
        <display value="Autoimmune interstitial lung disease-arthritis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444099" />
        <display value="Autosomal dominant spastic paraplegia type 73" />
      </concept>
      <concept>
        <code value="ORPHA:444116" />
        <display value="Hereditary amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:444138" />
        <display value="Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444316" />
        <display value="Idiopathic phalangeal acro-osteolysis" />
      </concept>
      <concept>
        <code value="ORPHA:444458" />
        <display value="Combined oxidative phosphorylation defect type 24" />
      </concept>
      <concept>
        <code value="ORPHA:444463" />
        <display value="Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444490" />
        <display value="Familial chylomicronemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:444916" />
        <display value="Pseudohypoaldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:444941" />
        <display value="Caudal regression-sirenomelia spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:445018" />
        <display value="Combined immunodeficiency due to LRBA deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:445038" />
        <display value="3-methylglutaconic aciduria type 7" />
      </concept>
      <concept>
        <code value="ORPHA:445062" />
        <display value="Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:445110" />
        <display value="Limb-girdle muscular dystrophy due to POMK deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:445197" />
        <display value="Secondary vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:446" />
        <display value="Neonatal hemochromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:447" />
        <display value="Paroxysmal nocturnal hemoglobinuria" />
      </concept>
      <concept>
        <code value="ORPHA:447731" />
        <display value="NIK deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:447737" />
        <display value="DOCK2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:447740" />
        <display value="Susceptibility to localized juvenile periodontitis" />
      </concept>
      <concept>
        <code value="ORPHA:447753" />
        <display value="Autosomal dominant spastic paraplegia type 9A" />
      </concept>
      <concept>
        <code value="ORPHA:447757" />
        <display value="Autosomal dominant spastic paraplegia type 9B" />
      </concept>
      <concept>
        <code value="ORPHA:447760" />
        <display value="Autosomal recessive spastic paraplegia type 9B" />
      </concept>
      <concept>
        <code value="ORPHA:447764" />
        <display value="IgG4-related sclerosing cholangitis" />
      </concept>
      <concept>
        <code value="ORPHA:447771" />
        <display value="Sclerosing cholangitis" />
      </concept>
      <concept>
        <code value="ORPHA:447774" />
        <display value="Secondary sclerosing cholangitis" />
      </concept>
      <concept>
        <code value="ORPHA:447777" />
        <display value="Keratocystic odontogenic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:447784" />
        <display value="Mitochondrial pyruvate carrier deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:447788" />
        <display value="Cerebral visual impairment" />
      </concept>
      <concept>
        <code value="ORPHA:447792" />
        <display value="Hemochromatosis type 5" />
      </concept>
      <concept>
        <code value="ORPHA:447795" />
        <display value="Lipoyl transferase 2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:447874" />
        <display value="Biological anomaly without phenotypic characterization" />
      </concept>
      <concept>
        <code value="ORPHA:447877" />
        <display value="Polymerase proofreading-related adenomatous polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:447881" />
        <display value="Idiopathic dropped head syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:447893" />
        <display value="Hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:447896" />
        <display value="Tremor-ataxia-central hypomyelination syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:447954" />
        <display value="Combined oxidative phosphorylation defect type 25" />
      </concept>
      <concept>
        <code value="ORPHA:447961" />
        <display value="Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:447964" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2V" />
      </concept>
      <concept>
        <code value="ORPHA:447974" />
        <display value="Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:447977" />
        <display value="Progressive scapulohumeroperoneal distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:447980" />
        <display value="19p13.3 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:447985" />
        <display value="Partial duplication of the short arm of chromosome 19" />
      </concept>
      <concept>
        <code value="ORPHA:447997" />
        <display value="Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:448" />
        <display value="Hemophilia" />
      </concept>
      <concept>
        <code value="ORPHA:448010" />
        <display value="CAD-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:448237" />
        <display value="Zika virus disease" />
      </concept>
      <concept>
        <code value="ORPHA:448242" />
        <display value="Autosomal recessive brachyolmia" />
      </concept>
      <concept>
        <code value="ORPHA:448251" />
        <display value="Progressive autosomal recessive ataxia-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:448264" />
        <display value="Isolated focal non-epidermolytic palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:448267" />
        <display value="Regressive spondylometaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:448270" />
        <display value="Ectopia cordis" />
      </concept>
      <concept>
        <code value="ORPHA:448348" />
        <display value="X-linked acrogigantism due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:448372" />
        <display value="X-linked acrogigantism due to Xq26 microduplication" />
      </concept>
      <concept>
        <code value="ORPHA:448426" />
        <display value="Genetic primary orthostatic hypotension" />
      </concept>
      <concept>
        <code value="ORPHA:44890" />
        <display value="Gastrointestinal stromal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:449" />
        <display value="Hepatoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:449266" />
        <display value="Pleural empyema" />
      </concept>
      <concept>
        <code value="ORPHA:449280" />
        <display value="Scedosporiosis" />
      </concept>
      <concept>
        <code value="ORPHA:449285" />
        <display value="Snakebite envenomation" />
      </concept>
      <concept>
        <code value="ORPHA:449291" />
        <display value="Symptomatic form of fragile X syndrome in female carrier" />
      </concept>
      <concept>
        <code value="ORPHA:449395" />
        <display value="IgG4-related kidney disease" />
      </concept>
      <concept>
        <code value="ORPHA:449400" />
        <display value="IgG4-related aortitis" />
      </concept>
      <concept>
        <code value="ORPHA:449427" />
        <display value="IgG4-related pachymeningitis" />
      </concept>
      <concept>
        <code value="ORPHA:449432" />
        <display value="IgG4-related submandibular gland disease" />
      </concept>
      <concept>
        <code value="ORPHA:449563" />
        <display value="IgG4-related ophthalmic disease" />
      </concept>
      <concept>
        <code value="ORPHA:449566" />
        <display value="Eosinophilic angiocentric fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:45" />
        <display value="Adenosine monophosphate deaminase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:450" />
        <display value="Heterotaxia" />
      </concept>
      <concept>
        <code value="ORPHA:450322" />
        <display value="Polyclonal hyperviscosity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:451602" />
        <display value="Primary cutaneous plasmacytosis" />
      </concept>
      <concept>
        <code value="ORPHA:451607" />
        <display value="Cutaneous pseudolymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:451612" />
        <display value="Familial congenital nasolacrimal duct obstruction" />
      </concept>
      <concept>
        <code value="ORPHA:452" />
        <display value="X-linked lissencephaly with abnormal genitalia" />
      </concept>
      <concept>
        <code value="ORPHA:453499" />
        <display value="Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:453504" />
        <display value="Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:453510" />
        <display value="Congenital insensitivity to pain with severe intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:453521" />
        <display value="Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:453533" />
        <display value="Polyendocrine-polyneuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:45358" />
        <display value="Congenital fibrosis of extraocular muscles" />
      </concept>
      <concept>
        <code value="ORPHA:454" />
        <display value="Acquired ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:45448" />
        <display value="Miyoshi myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:45452" />
        <display value="Idiopathic neonatal atrial flutter" />
      </concept>
      <concept>
        <code value="ORPHA:45453" />
        <display value="Incessant infant ventricular tachycardia" />
      </concept>
      <concept>
        <code value="ORPHA:454700" />
        <display value="Acquired Creutzfeldt-Jakob disease" />
      </concept>
      <concept>
        <code value="ORPHA:454706" />
        <display value="Progressive muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:454710" />
        <display value="Anti-p200 pemphigoid" />
      </concept>
      <concept>
        <code value="ORPHA:454714" />
        <display value="Plasma cell leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:454718" />
        <display value="Holmes-Adie syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:454723" />
        <display value="Endometrioid carcinoma of ovary" />
      </concept>
      <concept>
        <code value="ORPHA:454742" />
        <display value="Variably protease-sensitive prionopathy" />
      </concept>
      <concept>
        <code value="ORPHA:454745" />
        <display value="Kuru" />
      </concept>
      <concept>
        <code value="ORPHA:454750" />
        <display value="Isolated tracheoesophageal fistula" />
      </concept>
      <concept>
        <code value="ORPHA:454821" />
        <display value="Pleomorphic salivary gland adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:454836" />
        <display value="Avian influenza" />
      </concept>
      <concept>
        <code value="ORPHA:454840" />
        <display value="NTHL1-related attenuated familial adenomatous polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:454887" />
        <display value="Corticobasal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:455" />
        <display value="Superficial epidermolytic ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:456298" />
        <display value="1p35.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:456312" />
        <display value="Infantile multisystem neurologic-endocrine-pancreatic disease" />
      </concept>
      <concept>
        <code value="ORPHA:456318" />
        <display value="Hereditary sensory neuropathy-deafness-dementia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:456328" />
        <display value="X-linked myotubular myopathy-abnormal genitalia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:456333" />
        <display value="Hereditary neuroendocrine tumor of small intestine" />
      </concept>
      <concept>
        <code value="ORPHA:456369" />
        <display value="Polyglucosan body myopathy type 2" />
      </concept>
      <concept>
        <code value="ORPHA:457" />
        <display value="Harlequin ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:457050" />
        <display value="Autosomal dominant mitochondrial myopathy with exercise intolerance" />
      </concept>
      <concept>
        <code value="ORPHA:457059" />
        <display value="Pseudohypoparathyroidism with Albright hereditary osteodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:457062" />
        <display value="Pseudohypoparathyroidism without Albright hereditary osteodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:457074" />
        <display value="Congenital nemaline myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:457077" />
        <display value="TAFRO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457083" />
        <display value="Isolated splenogonadal fusion" />
      </concept>
      <concept>
        <code value="ORPHA:457088" />
        <display value="Predisposition to invasive fungal disease due to CARD9 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:457095" />
        <display value="Actinomycosis" />
      </concept>
      <concept>
        <code value="ORPHA:457185" />
        <display value="Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457193" />
        <display value="Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457205" />
        <display value="Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457212" />
        <display value="Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457223" />
        <display value="Syndromic sensorineural deafness due to combined oxidative phosphorylation defect" />
      </concept>
      <concept>
        <code value="ORPHA:457240" />
        <display value="X-linked intellectual disability-short stature-overweight syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457246" />
        <display value="Clear cell sarcoma of kidney" />
      </concept>
      <concept>
        <code value="ORPHA:457260" />
        <display value="X-linked intellectual disability-hypotonia-movement disorder syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457265" />
        <display value="Progressive myoclonic epilepsy type 9" />
      </concept>
      <concept>
        <code value="ORPHA:457279" />
        <display value="Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457284" />
        <display value="Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457351" />
        <display value="Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457359" />
        <display value="Megalencephaly-severe kyphoscoliosis-overgrowth syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457365" />
        <display value="Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457375" />
        <display value="ITPA-related encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:457378" />
        <display value="Complex lethal osteochondrodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:457395" />
        <display value="Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:457406" />
        <display value="Multiple mitochondrial dysfunctions syndrome type 4" />
      </concept>
      <concept>
        <code value="ORPHA:457485" />
        <display value="Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:458718" />
        <display value="Idiopathic spontaneous coronary artery dissection" />
      </concept>
      <concept>
        <code value="ORPHA:458758" />
        <display value="Composite hemangioendothelioma" />
      </concept>
      <concept>
        <code value="ORPHA:458763" />
        <display value="Retiform hemangioendothelioma" />
      </concept>
      <concept>
        <code value="ORPHA:458768" />
        <display value="Primary intralymphatic angioendothelioma" />
      </concept>
      <concept>
        <code value="ORPHA:458775" />
        <display value="Congenital hemangioma" />
      </concept>
      <concept>
        <code value="ORPHA:458785" />
        <display value="Partially involuting congenital hemangioma" />
      </concept>
      <concept>
        <code value="ORPHA:458792" />
        <display value="Mixed cystic lymphatic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:458798" />
        <display value="Spinocerebellar ataxia type 41" />
      </concept>
      <concept>
        <code value="ORPHA:458803" />
        <display value="Spinocerebellar ataxia type 42" />
      </concept>
      <concept>
        <code value="ORPHA:458827" />
        <display value="Vascular tumor with associated anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:458830" />
        <display value="Rare capillary malformation with associated anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:458833" />
        <display value="Common cystic lymphatic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:458837" />
        <display value="Rare combined vascular malformation" />
      </concept>
      <concept>
        <code value="ORPHA:458841" />
        <display value="Primary lymphedema with associated anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:458844" />
        <display value="Rare vascular malformation of major vessels" />
      </concept>
      <concept>
        <code value="ORPHA:459033" />
        <display value="Ataxia-oculomotor apraxia type 4" />
      </concept>
      <concept>
        <code value="ORPHA:459051" />
        <display value="Spondyloepiphyseal dysplasia, Stanescu type" />
      </concept>
      <concept>
        <code value="ORPHA:459056" />
        <display value="Autosomal recessive spastic paraplegia type 75" />
      </concept>
      <concept>
        <code value="ORPHA:459061" />
        <display value="Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:459070" />
        <display value="X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:459074" />
        <display value="Corpus callosum agenesis-macrocephaly-hypertelorism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:459345" />
        <display value="Immunodeficiency due to a complement cascade component deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:459348" />
        <display value="Immunodeficiency due to a complement regulatory deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:459353" />
        <display value="C1 inhibitor deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:459526" />
        <display value="Rare genetic capillary malformation" />
      </concept>
      <concept>
        <code value="ORPHA:459530" />
        <display value="Genetic primary lymphedema" />
      </concept>
      <concept>
        <code value="ORPHA:459537" />
        <display value="Genetic complex vascular malformation with associated anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:459543" />
        <display value="Rare genetic vascular tumor" />
      </concept>
      <concept>
        <code value="ORPHA:459548" />
        <display value="Rare genetic venous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:459787" />
        <display value="Lethal multiple congenital anomalies/dysmorphic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:46" />
        <display value="Adenylosuccinate lyase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:46059" />
        <display value="Lathosterolosis" />
      </concept>
      <concept>
        <code value="ORPHA:461" />
        <display value="Recessive X-linked ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:46135" />
        <display value="Primary central nervous system lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:46348" />
        <display value="Paroxysmal extreme pain disorder" />
      </concept>
      <concept>
        <code value="ORPHA:464" />
        <display value="Incontinentia pigmenti" />
      </concept>
      <concept>
        <code value="ORPHA:464282" />
        <display value="Spastic paraplegia-severe developmental delay-epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:464288" />
        <display value="Short stature-brachydactyly-obesity-global developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:464306" />
        <display value="DYRK1A-related intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:464311" />
        <display value="Intellectual disability syndrome due to a DYRK1A point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:464318" />
        <display value="Verrucous hemangioma" />
      </concept>
      <concept>
        <code value="ORPHA:464321" />
        <display value="Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:464329" />
        <display value="Kaposiform lymphangiomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:464336" />
        <display value="BENTA disease" />
      </concept>
      <concept>
        <code value="ORPHA:464343" />
        <display value="Catastrophic antiphospholipid syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:464359" />
        <display value="Benign metanephric tumour" />
      </concept>
      <concept>
        <code value="ORPHA:464366" />
        <display value="NEK9-related lethal skeletal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:464370" />
        <display value="Neonatal alloimmune neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:464440" />
        <display value="Primary dystonia, DYT27 type" />
      </concept>
      <concept>
        <code value="ORPHA:464443" />
        <display value="COG6-CGD" />
      </concept>
      <concept>
        <code value="ORPHA:464453" />
        <display value="Acquired methemoglobinemia" />
      </concept>
      <concept>
        <code value="ORPHA:464458" />
        <display value="Paracetamol poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:464724" />
        <display value="Fever-associated acute infantile liver failure syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:464738" />
        <display value="Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:464756" />
        <display value="Familial gastric type 1 neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:464760" />
        <display value="Familial cavitary optic disc anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:464764" />
        <display value="Immune-mediated acquired neuromuscular junction disease" />
      </concept>
      <concept>
        <code value="ORPHA:46484" />
        <display value="Oligodendroglial tumor" />
      </concept>
      <concept>
        <code value="ORPHA:46485" />
        <display value="Superficial pemphigus" />
      </concept>
      <concept>
        <code value="ORPHA:46486" />
        <display value="Mucous membrane pemphigoid" />
      </concept>
      <concept>
        <code value="ORPHA:46487" />
        <display value="Acquired epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:46488" />
        <display value="Linear IgA dermatosis" />
      </concept>
      <concept>
        <code value="ORPHA:465" />
        <display value="Congenital plasminogen activator inhibitor type 1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:46532" />
        <display value="Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:465508" />
        <display value="Symptomatic form of hemochromatosis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:465824" />
        <display value="Fetal encasement syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:466" />
        <display value="Fatal familial insomnia" />
      </concept>
      <concept>
        <code value="ORPHA:466026" />
        <display value="Class I glucose-6-phosphate dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:466066" />
        <display value="Genetic hemoglobinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:466084" />
        <display value="Genetic otorhinolaryngologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:46627" />
        <display value="Char syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:466650" />
        <display value="Exercise-induced malignant hyperthermia" />
      </concept>
      <concept>
        <code value="ORPHA:466658" />
        <display value="Rare disease with malignant hyperthermia" />
      </concept>
      <concept>
        <code value="ORPHA:466670" />
        <display value="Cyanide poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:466677" />
        <display value="Scorpion envenomation" />
      </concept>
      <concept>
        <code value="ORPHA:466682" />
        <display value="Euthyroid Graves orbitopathy" />
      </concept>
      <concept>
        <code value="ORPHA:466688" />
        <display value="Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:466695" />
        <display value="Supratip dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:466703" />
        <display value="TMEM199-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:466718" />
        <display value="Martinique crinkled retinal pigment epitheliopathy" />
      </concept>
      <concept>
        <code value="ORPHA:466722" />
        <display value="Autosomal recessive spastic paraplegia type 77" />
      </concept>
      <concept>
        <code value="ORPHA:466729" />
        <display value="Familial patent arterial duct" />
      </concept>
      <concept>
        <code value="ORPHA:466768" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2Z" />
      </concept>
      <concept>
        <code value="ORPHA:466775" />
        <display value="Autosomal recessive Charcot-Marie-Tooth disease type 2X" />
      </concept>
      <concept>
        <code value="ORPHA:466784" />
        <display value="Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect" />
      </concept>
      <concept>
        <code value="ORPHA:466791" />
        <display value="Macrocephaly-intellectual disability-left ventricular non compaction syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:466794" />
        <display value="Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:466801" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2W" />
      </concept>
      <concept>
        <code value="ORPHA:466806" />
        <display value="Autosomal dominant thrombocytopenia with platelet secretion defect" />
      </concept>
      <concept>
        <code value="ORPHA:466921" />
        <display value="Childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:466926" />
        <display value="Seizures-scoliosis-macrocephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:466934" />
        <display value="VPS11-related autosomal recessive hypomyelinating leukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:466943" />
        <display value="WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:466950" />
        <display value="Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:466962" />
        <display value="SMARCA4-deficient sarcoma of thorax" />
      </concept>
      <concept>
        <code value="ORPHA:467" />
        <display value="Non-acquired combined pituitary hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:467166" />
        <display value="Tubulinopathy-associated dysgyria" />
      </concept>
      <concept>
        <code value="ORPHA:467176" />
        <display value="Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:46724" />
        <display value="Cerebral arteriovenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:468620" />
        <display value="Intellectual disability-epilepsy-extrapyramidal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:468631" />
        <display value="Microcephalic primordial dwarfism due to RTTN deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:468635" />
        <display value="Cryptogenic multifocal ulcerous stenosing enteritis" />
      </concept>
      <concept>
        <code value="ORPHA:468641" />
        <display value="Chronic enteropathy associated with SLCO2A1 gene" />
      </concept>
      <concept>
        <code value="ORPHA:468661" />
        <display value="Autosomal recessive spastic paraplegia type 74" />
      </concept>
      <concept>
        <code value="ORPHA:468666" />
        <display value="Isolated generalized anhidrosis with normal sweat glands" />
      </concept>
      <concept>
        <code value="ORPHA:468672" />
        <display value="Colobomatous macrophthalmia-microcornea syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:468678" />
        <display value="Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:468684" />
        <display value="CCDC115-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:468699" />
        <display value="SLC39A8-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:468717" />
        <display value="Rhizomelic chondrodysplasia punctata type 5" />
      </concept>
      <concept>
        <code value="ORPHA:468726" />
        <display value="Severe primary trimethylaminuria" />
      </concept>
      <concept>
        <code value="ORPHA:469" />
        <display value="Hereditary fructose intolerance" />
      </concept>
      <concept>
        <code value="ORPHA:47" />
        <display value="X-linked agammaglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:470" />
        <display value="Lysinuric protein intolerance" />
      </concept>
      <concept>
        <code value="ORPHA:47044" />
        <display value="Hereditary papillary renal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:47045" />
        <display value="Familial cold urticaria" />
      </concept>
      <concept>
        <code value="ORPHA:471383" />
        <display value="Genetic lethal multiple congenital anomalies/dysmorphic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:47159" />
        <display value="Proximal renal tubular acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:472" />
        <display value="Isosporiasis" />
      </concept>
      <concept>
        <code value="ORPHA:474" />
        <display value="Jeune syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:474347" />
        <display value="Rare congenital anomaly of ventricular septum" />
      </concept>
      <concept>
        <code value="ORPHA:475" />
        <display value="Joubert syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:476084" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2X" />
      </concept>
      <concept>
        <code value="ORPHA:476093" />
        <display value="Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:476096" />
        <display value="Erythrokeratodermia-cardiomyopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:476102" />
        <display value="Hereditary pediatric Behcet-like disease" />
      </concept>
      <concept>
        <code value="ORPHA:476109" />
        <display value="Axonal hereditary motor and sensory neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:476113" />
        <display value="Combined immunodeficiency due to TFRC deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:476116" />
        <display value="Demyelinating hereditary motor and sensory neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:476119" />
        <display value="Autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:47612" />
        <display value="Felty syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:476123" />
        <display value="Intermediate Charcot-Marie-Tooth disease" />
      </concept>
      <concept>
        <code value="ORPHA:476126" />
        <display value="Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:476403" />
        <display value="Hypercontractile muscle stiffness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:476406" />
        <display value="Congenital generalized hypercontractile muscle stiffness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:477" />
        <display value="KID syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:477647" />
        <display value="Type 1 interferonopathy" />
      </concept>
      <concept>
        <code value="ORPHA:477650" />
        <display value="Fibroblastic rheumatism" />
      </concept>
      <concept>
        <code value="ORPHA:477661" />
        <display value="IL21-related infantile inflammatory bowel disease" />
      </concept>
      <concept>
        <code value="ORPHA:477673" />
        <display value="Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:477684" />
        <display value="Combined oxidative phosphorylation defect type 26" />
      </concept>
      <concept>
        <code value="ORPHA:477738" />
        <display value="Pediatric multiple sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:477742" />
        <display value="Nodular fasciitis" />
      </concept>
      <concept>
        <code value="ORPHA:477749" />
        <display value="Pontine autosomal dominant microangiopathy with leukoencephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:477754" />
        <display value="Genetic cerebral small vessel disease" />
      </concept>
      <concept>
        <code value="ORPHA:477759" />
        <display value="COL4A1 or COL4A2-related cerebral small vessel disease" />
      </concept>
      <concept>
        <code value="ORPHA:477762" />
        <display value="COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy" />
      </concept>
      <concept>
        <code value="ORPHA:477765" />
        <display value="COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy" />
      </concept>
      <concept>
        <code value="ORPHA:477768" />
        <display value="Moyomoya angiopathy" />
      </concept>
      <concept>
        <code value="ORPHA:477771" />
        <display value="Rare disorder with a moyamoya angiopathy" />
      </concept>
      <concept>
        <code value="ORPHA:477774" />
        <display value="Combined oxidative phosphorylation defect type 27" />
      </concept>
      <concept>
        <code value="ORPHA:477781" />
        <display value="Primary condylar hyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:477787" />
        <display value="Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder" />
      </concept>
      <concept>
        <code value="ORPHA:477794" />
        <display value="Syndromic constitutional thrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:477797" />
        <display value="Isolated constitutional thrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:477805" />
        <display value="Genetic cardiac malformation" />
      </concept>
      <concept>
        <code value="ORPHA:477808" />
        <display value="Other genetic dermis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:477811" />
        <display value="Rare hypercholesterolemia" />
      </concept>
      <concept>
        <code value="ORPHA:477814" />
        <display value="Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:477817" />
        <display value="PMP22-RAI1 contiguous gene duplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:477831" />
        <display value="Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:477857" />
        <display value="Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:477993" />
        <display value="Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:478" />
        <display value="Kallmann syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:478029" />
        <display value="Combined oxidative phosphorylation defect type 29" />
      </concept>
      <concept>
        <code value="ORPHA:478042" />
        <display value="Combined oxidative phosphorylation defect type 30" />
      </concept>
      <concept>
        <code value="ORPHA:478049" />
        <display value="Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:478664" />
        <display value="Hereditary sensory and autonomic neuropathy type 8" />
      </concept>
      <concept>
        <code value="ORPHA:48" />
        <display value="Congenital bilateral absence of vas deferens" />
      </concept>
      <concept>
        <code value="ORPHA:480" />
        <display value="Kearns-Sayre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:480476" />
        <display value="Progressive familial intrahepatic cholestasis type 5" />
      </concept>
      <concept>
        <code value="ORPHA:480483" />
        <display value="Progressive familial intrahepatic cholestasis type 4" />
      </concept>
      <concept>
        <code value="ORPHA:480491" />
        <display value="MYO5B-related progressive familial intrahepatic cholestasis" />
      </concept>
      <concept>
        <code value="ORPHA:480501" />
        <display value="Choledochal cyst" />
      </concept>
      <concept>
        <code value="ORPHA:480506" />
        <display value="Primary intrahepatic lithiasis" />
      </concept>
      <concept>
        <code value="ORPHA:480512" />
        <display value="Idiopathic ductopenia" />
      </concept>
      <concept>
        <code value="ORPHA:480520" />
        <display value="Caroli syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:480524" />
        <display value="Idiopathic peliosis hepatis" />
      </concept>
      <concept>
        <code value="ORPHA:480528" />
        <display value="Lethal hydranencephaly-diaphragmatic hernia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:480531" />
        <display value="Congenital portosystemic shunt" />
      </concept>
      <concept>
        <code value="ORPHA:480536" />
        <display value="MSH3-related attenuated familial adenomatous polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:480541" />
        <display value="High grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement" />
      </concept>
      <concept>
        <code value="ORPHA:480549" />
        <display value="Non-severe combined immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:480553" />
        <display value="Aneurysmal bone cyst" />
      </concept>
      <concept>
        <code value="ORPHA:480556" />
        <display value="Isolated neonatal sclerosing cholangitis" />
      </concept>
      <concept>
        <code value="ORPHA:480682" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2Z" />
      </concept>
      <concept>
        <code value="ORPHA:480701" />
        <display value="Facial diplegia with paresthesias" />
      </concept>
      <concept>
        <code value="ORPHA:480851" />
        <display value="Hereditary thrombocytopenia with early-onset myelofibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:480864" />
        <display value="Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:480880" />
        <display value="X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:480898" />
        <display value="Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:480907" />
        <display value="X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:481" />
        <display value="Kennedy disease" />
      </concept>
      <concept>
        <code value="ORPHA:48104" />
        <display value="Pyoderma gangrenosum" />
      </concept>
      <concept>
        <code value="ORPHA:481152" />
        <display value="PYCR2-related microcephaly-progressive leukoencephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:481508" />
        <display value="Gastroenteric neuroendocrine neoplasm" />
      </concept>
      <concept>
        <code value="ORPHA:48162" />
        <display value="Lewis-Sumner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:481662" />
        <display value="Familial Chilblain lupus" />
      </concept>
      <concept>
        <code value="ORPHA:481665" />
        <display value="USP18 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:481671" />
        <display value="Type 1 interferonopathy of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:481771" />
        <display value="Genetic alopecia" />
      </concept>
      <concept>
        <code value="ORPHA:481986" />
        <display value="Familial schizencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:482" />
        <display value="Kimura disease" />
      </concept>
      <concept>
        <code value="ORPHA:482072" />
        <display value="HTRA1-related cerebral small vessel disease" />
      </concept>
      <concept>
        <code value="ORPHA:482077" />
        <display value="HTRA1-related autosomal dominant cerebral small vessel disease" />
      </concept>
      <concept>
        <code value="ORPHA:482092" />
        <display value="Rare idiopathic macular telangiectasia" />
      </concept>
      <concept>
        <code value="ORPHA:482601" />
        <display value="Adenylosuccinate synthetase-like 1-related distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:482606" />
        <display value="X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:483" />
        <display value="Congenital high-molecular-weight kininogen deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:48372" />
        <display value="Nodular regenerative hyperplasia of the liver" />
      </concept>
      <concept>
        <code value="ORPHA:48377" />
        <display value="Subcorneal pustular dermatosis" />
      </concept>
      <concept>
        <code value="ORPHA:48431" />
        <display value="Congenital cataracts-facial dysmorphism-neuropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:48435" />
        <display value="Postinfectious vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:48471" />
        <display value="Lissencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:485" />
        <display value="Kniest dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:485275" />
        <display value="Acquired schizencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:485350" />
        <display value="CLCN4-related X-linked intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:485358" />
        <display value="Propylthiouracil embryofetopathy" />
      </concept>
      <concept>
        <code value="ORPHA:485382" />
        <display value="Genetic non-acquired premature ovarian failure" />
      </concept>
      <concept>
        <code value="ORPHA:485405" />
        <display value="16p12.1p12.3 triplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:485418" />
        <display value="EMILIN-1-related connective tissue disease" />
      </concept>
      <concept>
        <code value="ORPHA:485421" />
        <display value="MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect" />
      </concept>
      <concept>
        <code value="ORPHA:485426" />
        <display value="Isolated congenital hepatic fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:485631" />
        <display value="Congenital bile acid synthesis defect" />
      </concept>
      <concept>
        <code value="ORPHA:486" />
        <display value="Autosomal dominant severe congenital neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:48652" />
        <display value="Monosomy 22q13" />
      </concept>
      <concept>
        <code value="ORPHA:486811" />
        <display value="Prenatal-onset spinal muscular atrophy with congenital bone fractures" />
      </concept>
      <concept>
        <code value="ORPHA:486815" />
        <display value="Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:48686" />
        <display value="Primary effusion lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:486955" />
        <display value="Rare pediatric rheumatologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:487" />
        <display value="Krabbe disease" />
      </concept>
      <concept>
        <code value="ORPHA:48736" />
        <display value="Embryonal carcinoma of the central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:487796" />
        <display value="Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:487809" />
        <display value="Pediatric collagenous gastritis" />
      </concept>
      <concept>
        <code value="ORPHA:487814" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:487825" />
        <display value="Pierpont syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488" />
        <display value="Urachal cyst" />
      </concept>
      <concept>
        <code value="ORPHA:488168" />
        <display value="Microcephaly-congenital cataract-psoriasiform dermatitis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:48818" />
        <display value="Aceruloplasminemia" />
      </concept>
      <concept>
        <code value="ORPHA:488191" />
        <display value="Female infertility due to oocyte meiotic arrest" />
      </concept>
      <concept>
        <code value="ORPHA:488197" />
        <display value="Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488232" />
        <display value="Split-foot malformation-mesoaxial polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488239" />
        <display value="Acute macular neuroretinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:488265" />
        <display value="Osteofibrous dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:488280" />
        <display value="14q32 duplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488333" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2W" />
      </concept>
      <concept>
        <code value="ORPHA:488434" />
        <display value="Camptodactyly syndrome, Guadalajara type 3" />
      </concept>
      <concept>
        <code value="ORPHA:488437" />
        <display value="SIX2-related frontonasal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:488586" />
        <display value="Congenital amyoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:488594" />
        <display value="Autosomal recessive spastic paraplegia type 76" />
      </concept>
      <concept>
        <code value="ORPHA:488613" />
        <display value="Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488618" />
        <display value="Transketolase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:488627" />
        <display value="Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488632" />
        <display value="TBCK-related intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488635" />
        <display value="Early-onset epilepsy-intellectual disability-brain anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488642" />
        <display value="TELO2-related intellectual disability-neurodevelopmental disorder" />
      </concept>
      <concept>
        <code value="ORPHA:488647" />
        <display value="DDX41-related hematologic malignancy predisposition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:488650" />
        <display value="Distal myopathy, Tateyama type" />
      </concept>
      <concept>
        <code value="ORPHA:48918" />
        <display value="Focal myositis" />
      </concept>
      <concept>
        <code value="ORPHA:49" />
        <display value="Penile agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:490" />
        <display value="Omphalomesenteric cyst" />
      </concept>
      <concept>
        <code value="ORPHA:49041" />
        <display value="IgG4-related retroperitoneal fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:49042" />
        <display value="Dentinogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:492" />
        <display value="Proliferating trichilemmal cyst" />
      </concept>
      <concept>
        <code value="ORPHA:493" />
        <display value="Familial keratoacanthoma" />
      </concept>
      <concept>
        <code value="ORPHA:493342" />
        <display value="Vibratory urticaria" />
      </concept>
      <concept>
        <code value="ORPHA:493348" />
        <display value="Vibratory angioedema" />
      </concept>
      <concept>
        <code value="ORPHA:49382" />
        <display value="Achromatopsia" />
      </concept>
      <concept>
        <code value="ORPHA:494" />
        <display value="Keratoderma hereditarium mutilans" />
      </concept>
      <concept>
        <code value="ORPHA:494344" />
        <display value="RERE-related neurodevelopmental syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:494348" />
        <display value="Early-onset familial noncirrhotic portal hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:494418" />
        <display value="Vulvar carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:494421" />
        <display value="Sacrococcygeal teratoma" />
      </concept>
      <concept>
        <code value="ORPHA:494424" />
        <display value="Extracranial carotid artery aneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:494428" />
        <display value="Idiopathic pleuroparenchymal fibroelastosis" />
      </concept>
      <concept>
        <code value="ORPHA:494433" />
        <display value="MIRAGE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:494439" />
        <display value="Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:494444" />
        <display value="DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:494448" />
        <display value="Vulvar squamous cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:494451" />
        <display value="Vulvar basal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:494454" />
        <display value="Vulvar adenocarcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:494457" />
        <display value="Rare hyperkinetic movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:494526" />
        <display value="Infantile-onset generalized dyskinesia with orofacial involvement" />
      </concept>
      <concept>
        <code value="ORPHA:494541" />
        <display value="Childhood-onset benign chorea with striatal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:494547" />
        <display value="Squamous cell carcinoma of the hypopharynx" />
      </concept>
      <concept>
        <code value="ORPHA:494550" />
        <display value="Squamous cell carcinoma of the larynx" />
      </concept>
      <concept>
        <code value="ORPHA:495" />
        <display value="Transgrediens et progrediens palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:495274" />
        <display value="Charcot-Marie-Tooth disease type 2T" />
      </concept>
      <concept>
        <code value="ORPHA:49566" />
        <display value="Acquired purpura fulminans" />
      </concept>
      <concept>
        <code value="ORPHA:495818" />
        <display value="9q33.3q34.11 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:495844" />
        <display value="C11ORF73-related autosomal recessive hypomyelinating leukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:495875" />
        <display value="Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:495879" />
        <display value="Congenital agenesis of the scrotum" />
      </concept>
      <concept>
        <code value="ORPHA:495930" />
        <display value="Familial monosomy 7 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:496641" />
        <display value="Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:496686" />
        <display value="Kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:496689" />
        <display value="Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:496693" />
        <display value="Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:496751" />
        <display value="EVEN-plus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:496756" />
        <display value="Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:496790" />
        <display value="Optic atrophy-peripheral neuropathy-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:496916" />
        <display value="Rare genetic hyperkinetic movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:496924" />
        <display value="Non-inflammatory vasculopathy" />
      </concept>
      <concept>
        <code value="ORPHA:497188" />
        <display value="Diffuse intrinsic pontine glioma" />
      </concept>
      <concept>
        <code value="ORPHA:497623" />
        <display value="C12ORF65-related combined oxidative phosphorylation defect" />
      </concept>
      <concept>
        <code value="ORPHA:497737" />
        <display value="Epidermolytic nevus" />
      </concept>
      <concept>
        <code value="ORPHA:497757" />
        <display value="MME-related autosomal dominant Charcot Marie Tooth disease type 2" />
      </concept>
      <concept>
        <code value="ORPHA:497764" />
        <display value="Spinocerebellar ataxia type 43" />
      </concept>
      <concept>
        <code value="ORPHA:497906" />
        <display value="Childhood-onset basal ganglia degeneration syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:498" />
        <display value="Keratosis pilaris atrophicans" />
      </concept>
      <concept>
        <code value="ORPHA:49804" />
        <display value="Lichen amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:498228" />
        <display value="Phyllodes tumor of the prostate" />
      </concept>
      <concept>
        <code value="ORPHA:498251" />
        <display value="Menstrual cycle-dependent periodic fever" />
      </concept>
      <concept>
        <code value="ORPHA:49827" />
        <display value="Thiamine-responsive megaloblastic anemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:498345" />
        <display value="Biliary atresia and associated disorders" />
      </concept>
      <concept>
        <code value="ORPHA:498350" />
        <display value="Syndromic biliary atresia" />
      </concept>
      <concept>
        <code value="ORPHA:498359" />
        <display value="Aquagenic palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:498445" />
        <display value="Genetic inflammatory or rheumatoid-like osteoarthropathy" />
      </concept>
      <concept>
        <code value="ORPHA:498448" />
        <display value="Overgrowth or tall stature syndrome with skeletal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:498451" />
        <display value="Dysostosis with brachydactyly without extraskeletal manifestations" />
      </concept>
      <concept>
        <code value="ORPHA:498454" />
        <display value="Dysostosis with brachydactyly with extraskeletal manifestations" />
      </concept>
      <concept>
        <code value="ORPHA:498457" />
        <display value="Longitudinal limb defect" />
      </concept>
      <concept>
        <code value="ORPHA:498461" />
        <display value="Terminal transverse limb defect" />
      </concept>
      <concept>
        <code value="ORPHA:498464" />
        <display value="Non-syndromic preaxial polydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:498467" />
        <display value="Non-syndromic postaxial polydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:498470" />
        <display value="Non-syndromic complex polydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:498474" />
        <display value="Hyaline fibromatosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:498477" />
        <display value="Ectrodactyly with and without other manifestations" />
      </concept>
      <concept>
        <code value="ORPHA:498481" />
        <display value="LRP5-related primary osteoporosis" />
      </concept>
      <concept>
        <code value="ORPHA:498485" />
        <display value="Overgrowth-metaphyseal undermodeling-spondylar dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:498488" />
        <display value="Overgrowth syndrome with 2q37 translocation" />
      </concept>
      <concept>
        <code value="ORPHA:498491" />
        <display value="Complete hemimelia" />
      </concept>
      <concept>
        <code value="ORPHA:498494" />
        <display value="Mirror-image polydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:498497" />
        <display value="Short rib-polydactyly syndrome type 5" />
      </concept>
      <concept>
        <code value="ORPHA:498602" />
        <display value="Sugarman brachydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:498693" />
        <display value="MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:498700" />
        <display value="Limbic encephalitis with neurexin-3 antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:499" />
        <display value="Kerion celsi" />
      </concept>
      <concept>
        <code value="ORPHA:499004" />
        <display value="Tuberculous meningitis" />
      </concept>
      <concept>
        <code value="ORPHA:499009" />
        <display value="Congenital syphilis" />
      </concept>
      <concept>
        <code value="ORPHA:499047" />
        <display value="Autoimmune/inflammatory optic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:499085" />
        <display value="Chronic relapsing inflammatory optic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:499096" />
        <display value="Isolated optic neuritis" />
      </concept>
      <concept>
        <code value="ORPHA:499103" />
        <display value="Recurrent idiopathic neuroretinitis" />
      </concept>
      <concept>
        <code value="ORPHA:499107" />
        <display value="Optic perineuritis" />
      </concept>
      <concept>
        <code value="ORPHA:499182" />
        <display value="Pilomatrix carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:5" />
        <display value="Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:50" />
        <display value="Aicardi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500" />
        <display value="Noonan syndrome with multiple lentigines" />
      </concept>
      <concept>
        <code value="ORPHA:500055" />
        <display value="16p13.2 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500062" />
        <display value="Infantile-onset periodic fever-panniculitis-dermatosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500095" />
        <display value="Tall stature-intellectual disability-renal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500135" />
        <display value="Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500144" />
        <display value="Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500150" />
        <display value="Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500159" />
        <display value="Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom" />
      </concept>
      <concept>
        <code value="ORPHA:500163" />
        <display value="SIN3A-related intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500166" />
        <display value="SIN3A-related intellectual disability syndrome due to a point mutation" />
      </concept>
      <concept>
        <code value="ORPHA:500180" />
        <display value="Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:500188" />
        <display value="X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500464" />
        <display value="Squamous cell carcinoma of the nasal cavity and paranasal sinuses" />
      </concept>
      <concept>
        <code value="ORPHA:500478" />
        <display value="Squamous cell carcinoma of the oropharynx" />
      </concept>
      <concept>
        <code value="ORPHA:500481" />
        <display value="Squamous cell carcinoma of salivary glands" />
      </concept>
      <concept>
        <code value="ORPHA:500533" />
        <display value="Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:500545" />
        <display value="Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract" />
      </concept>
      <concept>
        <code value="ORPHA:500548" />
        <display value="Osteosclerotic metaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:501" />
        <display value="Lafora disease" />
      </concept>
      <concept>
        <code value="ORPHA:502" />
        <display value="Trichorhinophalangeal syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:502305" />
        <display value="Cochleovestibular dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:502318" />
        <display value="Cochlear nerve deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:502363" />
        <display value="Squamous cell carcinoma of the oral cavity" />
      </concept>
      <concept>
        <code value="ORPHA:502366" />
        <display value="Squamous cell carcinoma of the lip" />
      </concept>
      <concept>
        <code value="ORPHA:502369" />
        <display value="Squamous cell carcinoma of oral cavity and lip" />
      </concept>
      <concept>
        <code value="ORPHA:502423" />
        <display value="Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:502430" />
        <display value="Metopic ridging-ptosis-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:502434" />
        <display value="STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:502437" />
        <display value="4q25 proximal deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:502444" />
        <display value="Alkaline ceramidase 3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:502499" />
        <display value="Erythema multiforme major" />
      </concept>
      <concept>
        <code value="ORPHA:50251" />
        <display value="Pleural mesothelioma" />
      </concept>
      <concept>
        <code value="ORPHA:503" />
        <display value="Autosomal dominant Larsen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:504" />
        <display value="Creeping myiasis" />
      </concept>
      <concept>
        <code value="ORPHA:504476" />
        <display value="Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:504523" />
        <display value="Severe combined immunodeficiency due to LAT deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:504530" />
        <display value="Combined immunodeficiency due to Moesin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:505" />
        <display value="Graham Little-Piccardi-Lassueur syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:505208" />
        <display value="3-methylglutaconic aciduria type 8" />
      </concept>
      <concept>
        <code value="ORPHA:505216" />
        <display value="3-methylglutaconic aciduria type 9" />
      </concept>
      <concept>
        <code value="ORPHA:505227" />
        <display value="Combined immunodeficiency due to GINS1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:505237" />
        <display value="Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:505242" />
        <display value="Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:505248" />
        <display value="Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders" />
      </concept>
      <concept>
        <code value="ORPHA:505395" />
        <display value="Ventilator-induced diaphragmatic dysfunction" />
      </concept>
      <concept>
        <code value="ORPHA:505652" />
        <display value="CDKL5-related epileptic encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:506" />
        <display value="Leigh syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:506052" />
        <display value="Neuroendocrine neoplasm of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:506060" />
        <display value="Functioning neuroendocrine tumor of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:506075" />
        <display value="Non-functioning neuroendocrine tumor of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:506090" />
        <display value="Serotonin-producing neuroendocrine tumor of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:506098" />
        <display value="Neuroendocrine carcinoma of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:506112" />
        <display value="Mixed neuroendocrine-nonneuroendocrine neoplasm of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:506136" />
        <display value="Neuroendocrine neoplasm of esophagus" />
      </concept>
      <concept>
        <code value="ORPHA:506307" />
        <display value="Stromme syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:506334" />
        <display value="Familial steroid-resistant nephrotic syndrome with adrenal insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:506353" />
        <display value="Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction" />
      </concept>
      <concept>
        <code value="ORPHA:506358" />
        <display value="Gabriele-de Vries syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:506784" />
        <display value="Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:507" />
        <display value="Leishmaniasis" />
      </concept>
      <concept>
        <code value="ORPHA:508" />
        <display value="Leprechaunism" />
      </concept>
      <concept>
        <code value="ORPHA:50809" />
        <display value="Talo-patello-scaphoid osteolysis" />
      </concept>
      <concept>
        <code value="ORPHA:508093" />
        <display value="MEPAN syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:50810" />
        <display value="Microlissencephaly-micromelia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:50811" />
        <display value="Lipodystrophy-intellectual disability-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:50812" />
        <display value="Zellweger-like syndrome without peroxisomal anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:50814" />
        <display value="Craniolenticulosutural dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:50815" />
        <display value="Branchiogenic deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:50817" />
        <display value="Duane anomaly-myopathy-scoliosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:50839" />
        <display value="Cat-scratch disease" />
      </concept>
      <concept>
        <code value="ORPHA:508410" />
        <display value="Familial intestinal malrotation" />
      </concept>
      <concept>
        <code value="ORPHA:508476" />
        <display value="Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:508488" />
        <display value="8q24.3 deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:508498" />
        <display value="Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:508501" />
        <display value="Oral-facial-digital syndrome with short stature and brachymesophalangy" />
      </concept>
      <concept>
        <code value="ORPHA:508512" />
        <display value="Congenital multiple cafe-au-lait macules-increased sister chromatid exchange syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:508523" />
        <display value="Hyperphenylalaninemia due to DNAJC12 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:508529" />
        <display value="Generalized basal epidermolysis bullosa simplex with skin atrophy, scarring and hair loss" />
      </concept>
      <concept>
        <code value="ORPHA:508533" />
        <display value="Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:508542" />
        <display value="Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:509" />
        <display value="Leptospirosis" />
      </concept>
      <concept>
        <code value="ORPHA:50918" />
        <display value="Kikuchi-Fujimoto disease" />
      </concept>
      <concept>
        <code value="ORPHA:50920" />
        <display value="Multiple fibroadenoma of the breast" />
      </concept>
      <concept>
        <code value="ORPHA:50942" />
        <display value="Striate palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:50943" />
        <display value="Keratolytic winter erythema" />
      </concept>
      <concept>
        <code value="ORPHA:50944" />
        <display value="Schopf-Schulz-Passarge syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:50945" />
        <display value="Blomstrand lethal chondrodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:51" />
        <display value="Aicardi-Goutiares syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:510" />
        <display value="Lesch-Nyhan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:51083" />
        <display value="Familial short QT syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:51084" />
        <display value="Torsade-de-pointes syndrome with short coupling interval" />
      </concept>
      <concept>
        <code value="ORPHA:511" />
        <display value="Maple syrup urine disease" />
      </concept>
      <concept>
        <code value="ORPHA:51188" />
        <display value="Ethylmalonic encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:512" />
        <display value="Metachromatic leukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:512017" />
        <display value="Chronic lymphoproliferative disorder of natural killer cells" />
      </concept>
      <concept>
        <code value="ORPHA:512034" />
        <display value="Large granular lymphocyte leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:51208" />
        <display value="Formiminoglutamic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:512103" />
        <display value="Autosomal recessive epidermolytic ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:512260" />
        <display value="Congenital cerebellar ataxia due to RNU12 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:513" />
        <display value="Acute lymphoblastic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:513436" />
        <display value="Autosomal recessive spastic paraplegia type 78" />
      </concept>
      <concept>
        <code value="ORPHA:513456" />
        <display value="Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:514" />
        <display value="Acute monoblastic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:514352" />
        <display value="Congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:514980" />
        <display value="ATP13A2-related parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:51577" />
        <display value="Cobblestone lissencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:51608" />
        <display value="Generalized arterial calcification of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:51636" />
        <display value="WHIM syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:517" />
        <display value="Acute myelomonocytic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:518" />
        <display value="Acute megakaryoblastic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:51890" />
        <display value="Anterior cutaneous nerve entrapment syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:519" />
        <display value="Acute myeloid leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:519264" />
        <display value="Inflammatory/autoimmune disorder involving the lacrimal system" />
      </concept>
      <concept>
        <code value="ORPHA:519266" />
        <display value="Rare disorder of the ocular adnexa" />
      </concept>
      <concept>
        <code value="ORPHA:519268" />
        <display value="Rare disorder with ectropion" />
      </concept>
      <concept>
        <code value="ORPHA:519270" />
        <display value="Rare disorder with entropion" />
      </concept>
      <concept>
        <code value="ORPHA:519272" />
        <display value="Structural developmental eye defect" />
      </concept>
      <concept>
        <code value="ORPHA:519274" />
        <display value="Syndromic lacrimal system disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519276" />
        <display value="Anterior segment developmental abnormality with extraocular manifestations" />
      </concept>
      <concept>
        <code value="ORPHA:519278" />
        <display value="Infective keratitis" />
      </concept>
      <concept>
        <code value="ORPHA:519280" />
        <display value="Rare conjunctivitis" />
      </concept>
      <concept>
        <code value="ORPHA:519282" />
        <display value="Rare corneal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519284" />
        <display value="Rare disorder of the anterior segment of the eye" />
      </concept>
      <concept>
        <code value="ORPHA:519286" />
        <display value="Rare disorder of the pupil" />
      </concept>
      <concept>
        <code value="ORPHA:519288" />
        <display value="Rare disorder with corneal involvement as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:519290" />
        <display value="Rare inflammatory/autoimmune corneal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519292" />
        <display value="Syndromic ectopia lentis" />
      </concept>
      <concept>
        <code value="ORPHA:519294" />
        <display value="Syndromic microspherophakia" />
      </concept>
      <concept>
        <code value="ORPHA:519296" />
        <display value="Rare disorder with pigmented sclera" />
      </concept>
      <concept>
        <code value="ORPHA:519298" />
        <display value="Rare scleral disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519300" />
        <display value="Isolated chorioretinal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:519302" />
        <display value="Isolated macular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:519304" />
        <display value="Isolated vitreoretinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:519306" />
        <display value="Isolated progressive inherited retinal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519309" />
        <display value="Rare choroidal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519311" />
        <display value="Rare disorder of the posterior segment of the eye" />
      </concept>
      <concept>
        <code value="ORPHA:519313" />
        <display value="Rare macular disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519315" />
        <display value="Rare retinal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519317" />
        <display value="Rare retinal vasculopathy" />
      </concept>
      <concept>
        <code value="ORPHA:519319" />
        <display value="Isolated stationary inherited retinal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519321" />
        <display value="Syndromic chorioretinal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:519323" />
        <display value="Syndromic macular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:519325" />
        <display value="Syndromic inherited retinal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519327" />
        <display value="Syndromic vitreoretinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:519329" />
        <display value="Rare disorder involving multiple structures of the eye" />
      </concept>
      <concept>
        <code value="ORPHA:519331" />
        <display value="Secondary early-onset glaucoma" />
      </concept>
      <concept>
        <code value="ORPHA:519333" />
        <display value="Congenital optic disc excavation" />
      </concept>
      <concept>
        <code value="ORPHA:519337" />
        <display value="Disorder with optic nerve compression" />
      </concept>
      <concept>
        <code value="ORPHA:519339" />
        <display value="Pseudopapilledema" />
      </concept>
      <concept>
        <code value="ORPHA:519341" />
        <display value="Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:519343" />
        <display value="Rare ophthalmic disorder with cortical involvement" />
      </concept>
      <concept>
        <code value="ORPHA:519345" />
        <display value="Rare disorder with optic disc malformation" />
      </concept>
      <concept>
        <code value="ORPHA:519347" />
        <display value="Rare neuromuscular disorder with ocular motility/alignment anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:519349" />
        <display value="Rare ophthalmic disorder with cranial nerve involvement" />
      </concept>
      <concept>
        <code value="ORPHA:519351" />
        <display value="Rare optic nerve disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519353" />
        <display value="Rare trochlear nerve disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519355" />
        <display value="Rare ocular motility/alignment disorder" />
      </concept>
      <concept>
        <code value="ORPHA:519386" />
        <display value="Isolated congenital entropion" />
      </concept>
      <concept>
        <code value="ORPHA:519388" />
        <display value="Autosomal recessive anterior segment dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:519390" />
        <display value="Isolated blepharochalasis" />
      </concept>
      <concept>
        <code value="ORPHA:519392" />
        <display value="Isolated iridoschisis" />
      </concept>
      <concept>
        <code value="ORPHA:519396" />
        <display value="Isolated microspherophakia" />
      </concept>
      <concept>
        <code value="ORPHA:519398" />
        <display value="Isolated foveal hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:519400" />
        <display value="Peripapillary staphyloma" />
      </concept>
      <concept>
        <code value="ORPHA:519402" />
        <display value="Isolated megalopapilla" />
      </concept>
      <concept>
        <code value="ORPHA:519404" />
        <display value="Optic disc pit" />
      </concept>
      <concept>
        <code value="ORPHA:519406" />
        <display value="Thygeson superficial punctate keratopathy" />
      </concept>
      <concept>
        <code value="ORPHA:519408" />
        <display value="Mooren ulcer" />
      </concept>
      <concept>
        <code value="ORPHA:519410" />
        <display value="Terrien marginal degeneration" />
      </concept>
      <concept>
        <code value="ORPHA:519930" />
        <display value="Fungal keratitis" />
      </concept>
      <concept>
        <code value="ORPHA:52" />
        <display value="Alagille syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:520" />
        <display value="Acute promyelocytic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:52022" />
        <display value="Potocki-Shaffer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:52047" />
        <display value="Braddock syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:52054" />
        <display value="Craniosynostosis-intracranial calcifications syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:52055" />
        <display value="Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:52056" />
        <display value="Ulnar/fibula ray defect-brachydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:520814" />
        <display value="Rare disorder of the visual organs" />
      </concept>
      <concept>
        <code value="ORPHA:520817" />
        <display value="Isolated inherited retinal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:520820" />
        <display value="Progressive external ophthalmoplegia" />
      </concept>
      <concept>
        <code value="ORPHA:521" />
        <display value="Chronic myeloid leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:521123" />
        <display value="Radiation-induced plexopathy" />
      </concept>
      <concept>
        <code value="ORPHA:521127" />
        <display value="Osteoradionecrosis of the mandible" />
      </concept>
      <concept>
        <code value="ORPHA:521132" />
        <display value="Radiation-induced disorder" />
      </concept>
      <concept>
        <code value="ORPHA:521219" />
        <display value="Mirizzi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:521232" />
        <display value="Genetic primary orthostatic disorder" />
      </concept>
      <concept>
        <code value="ORPHA:521236" />
        <display value="Primary orthostatic disorder" />
      </concept>
      <concept>
        <code value="ORPHA:521258" />
        <display value="Xq25 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:521305" />
        <display value="Proximal myopathy with focal depletion of mitochondria" />
      </concept>
      <concept>
        <code value="ORPHA:521308" />
        <display value="Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:521390" />
        <display value="Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:521406" />
        <display value="Dystonia-parkinsonism-hypermanganesemia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:521411" />
        <display value="Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism deffect" />
      </concept>
      <concept>
        <code value="ORPHA:521414" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2DD" />
      </concept>
      <concept>
        <code value="ORPHA:521426" />
        <display value="PLAA-associated neurodevelopmental disorder" />
      </concept>
      <concept>
        <code value="ORPHA:521432" />
        <display value="Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:521438" />
        <display value="Congenital vertebral-cardiac-renal anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:521445" />
        <display value="Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:521450" />
        <display value="LAMA5-related multisystemic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:522037" />
        <display value="Primary autoimmune enteropathy" />
      </concept>
      <concept>
        <code value="ORPHA:522043" />
        <display value="Syndromic autoimmune enteropathy" />
      </concept>
      <concept>
        <code value="ORPHA:522077" />
        <display value="Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:522504" />
        <display value="Rare genetic disorder of the visual organs" />
      </concept>
      <concept>
        <code value="ORPHA:522506" />
        <display value="Rare genetic brainstem or cerebellar disorder with ophthalmic involvement as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:522508" />
        <display value="Rare genetic ophthalmic disorder with cortical involvement" />
      </concept>
      <concept>
        <code value="ORPHA:522510" />
        <display value="Rare genetic ophthalmic disorder with cranial nerve involvement" />
      </concept>
      <concept>
        <code value="ORPHA:522512" />
        <display value="Rare genetic optic nerve disorder" />
      </concept>
      <concept>
        <code value="ORPHA:522514" />
        <display value="Congenital optic disc excavation of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:522516" />
        <display value="Rare genetic ocular motility/alignment disorder" />
      </concept>
      <concept>
        <code value="ORPHA:522518" />
        <display value="Rare genetic disorder with strabismus" />
      </concept>
      <concept>
        <code value="ORPHA:522520" />
        <display value="Syndromic genetic disorder with strabismus" />
      </concept>
      <concept>
        <code value="ORPHA:522522" />
        <display value="Rare genetic neuromuscular disorder with ocular motility/alignment anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:522524" />
        <display value="Rare genetic disorder of the ocular adnexa" />
      </concept>
      <concept>
        <code value="ORPHA:522526" />
        <display value="Rare genetic palpebral disorder" />
      </concept>
      <concept>
        <code value="ORPHA:522528" />
        <display value="Rare genetic eyelid malposition disorder" />
      </concept>
      <concept>
        <code value="ORPHA:522530" />
        <display value="Rare genetic disorder with entropion" />
      </concept>
      <concept>
        <code value="ORPHA:522532" />
        <display value="Rare genetic disorder of the lacrimal apparatus" />
      </concept>
      <concept>
        <code value="ORPHA:522534" />
        <display value="Lacrimal drainage system anomaly of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:522536" />
        <display value="Structural developmental eye defect of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:522538" />
        <display value="Rare genetic disorder of the anterior segment of the eye" />
      </concept>
      <concept>
        <code value="ORPHA:522540" />
        <display value="Anterior segment developmental anomaly of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:522542" />
        <display value="Rare genetic disorder with conjunctival involvement as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:522544" />
        <display value="Rare genetic conjunctivitis" />
      </concept>
      <concept>
        <code value="ORPHA:522546" />
        <display value="Rare genetic disorder with lens opacification" />
      </concept>
      <concept>
        <code value="ORPHA:522548" />
        <display value="Syndromic genetic cataract" />
      </concept>
      <concept>
        <code value="ORPHA:522550" />
        <display value="Lens size anomaly of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:522552" />
        <display value="Lens position anomaly of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:522554" />
        <display value="Syndromic genetic ectopia lentis" />
      </concept>
      <concept>
        <code value="ORPHA:522556" />
        <display value="Rare genetic corneal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:522558" />
        <display value="Rare genetic disorder with corneal involvement as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:522560" />
        <display value="Genetic corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:522562" />
        <display value="Genetic superficial corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:522564" />
        <display value="Syndromic genetic keratoconus" />
      </concept>
      <concept>
        <code value="ORPHA:522566" />
        <display value="Rare genetic inflammatory/autoimmune corneal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:522568" />
        <display value="Rare genetic disorder of the pupil" />
      </concept>
      <concept>
        <code value="ORPHA:522570" />
        <display value="Rare genetic disorder of the posterior segment of the eye" />
      </concept>
      <concept>
        <code value="ORPHA:522572" />
        <display value="Rare genetic retinal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:522574" />
        <display value="Rare genetic macular disorder" />
      </concept>
      <concept>
        <code value="ORPHA:522576" />
        <display value="Rare genetic retinal vasculopathy" />
      </concept>
      <concept>
        <code value="ORPHA:522578" />
        <display value="Rare genetic disorder involving multiple structures of the eye" />
      </concept>
      <concept>
        <code value="ORPHA:522580" />
        <display value="Secondary early-onset glaucoma of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:522584" />
        <display value="Rare genetic choroidal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:523" />
        <display value="Hereditary leiomyomatosis and renal cell cancer" />
      </concept>
      <concept>
        <code value="ORPHA:523000" />
        <display value="Pediatric-onset glaucoma" />
      </concept>
      <concept>
        <code value="ORPHA:52368" />
        <display value="Mohr-Tranebjaerg syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:524" />
        <display value="Li-Fraumeni syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:52416" />
        <display value="Mantle cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:52417" />
        <display value="MALT lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:52427" />
        <display value="Retinitis punctata albescens" />
      </concept>
      <concept>
        <code value="ORPHA:52429" />
        <display value="Branchiootic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:52430" />
        <display value="Inclusion body myopathy with Paget disease of bone and frontotemporal dementia" />
      </concept>
      <concept>
        <code value="ORPHA:525" />
        <display value="Lichen planopilaris" />
      </concept>
      <concept>
        <code value="ORPHA:52503" />
        <display value="X-linked creatine transporter deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:52530" />
        <display value="Pseudo-von Willebrand disease" />
      </concept>
      <concept>
        <code value="ORPHA:525677" />
        <display value="Genetic congenital malformation of the eye with glaucoma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:525731" />
        <display value="Pediatric-onset Graves disease" />
      </concept>
      <concept>
        <code value="ORPHA:525738" />
        <display value="Prepubertal anorexia nervosa" />
      </concept>
      <concept>
        <code value="ORPHA:526" />
        <display value="Liddle syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:52662" />
        <display value="Rare teratologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:52688" />
        <display value="Myelodysplastic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:527276" />
        <display value="Encephalopathy due to mitochondrial and peroxisomal fission defect" />
      </concept>
      <concept>
        <code value="ORPHA:52759" />
        <display value="Vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:528" />
        <display value="Berardinelli-Seip congenital lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:529" />
        <display value="Roch-Leri mesosomatous lipomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:52901" />
        <display value="Isolated follicle stimulating hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:52994" />
        <display value="Orbital leiomyoma" />
      </concept>
      <concept>
        <code value="ORPHA:53" />
        <display value="Albers-Schonberg osteopetrosis" />
      </concept>
      <concept>
        <code value="ORPHA:530" />
        <display value="Lipoid proteinosis" />
      </concept>
      <concept>
        <code value="ORPHA:53035" />
        <display value="Caroli disease" />
      </concept>
      <concept>
        <code value="ORPHA:531" />
        <display value="Miller-Dieker syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:53271" />
        <display value="Muenke syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:53296" />
        <display value="Familial cutaneous collagenoma" />
      </concept>
      <concept>
        <code value="ORPHA:533" />
        <display value="Listeriosis" />
      </concept>
      <concept>
        <code value="ORPHA:53347" />
        <display value="Brody myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:53351" />
        <display value="X-linked dystonia-parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:53372" />
        <display value="Hereditary geniospasm" />
      </concept>
      <concept>
        <code value="ORPHA:534" />
        <display value="Oculocerebrorenal syndrome of Lowe" />
      </concept>
      <concept>
        <code value="ORPHA:535" />
        <display value="Rare cutaneous lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:53540" />
        <display value="Goldmann-Favre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:53583" />
        <display value="Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity" />
      </concept>
      <concept>
        <code value="ORPHA:536" />
        <display value="Systemic lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:53689" />
        <display value="Congenital chloride diarrhea" />
      </concept>
      <concept>
        <code value="ORPHA:53690" />
        <display value="Congenital lactase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:53691" />
        <display value="Congenital cornea plana" />
      </concept>
      <concept>
        <code value="ORPHA:53693" />
        <display value="GRACILE syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:53696" />
        <display value="Lethal arthrogryposis-anterior horn cell disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:53697" />
        <display value="Gnathodiaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:53698" />
        <display value="Hyaline body myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:537" />
        <display value="Toxic epidermal necrolysis" />
      </concept>
      <concept>
        <code value="ORPHA:53715" />
        <display value="Familial tumoral calcinosis" />
      </concept>
      <concept>
        <code value="ORPHA:53719" />
        <display value="Wyburn-Mason syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:53721" />
        <display value="Cobb syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:53739" />
        <display value="Distal hereditary motor neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:538" />
        <display value="Lymphangioleiomyomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:54" />
        <display value="X-linked recessive ocular albinism" />
      </concept>
      <concept>
        <code value="ORPHA:540" />
        <display value="Familial hemophagocytic lymphohistiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:54028" />
        <display value="Plummer-Vinson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:54057" />
        <display value="Thrombotic thrombocytopenic purpura" />
      </concept>
      <concept>
        <code value="ORPHA:541" />
        <display value="Primary cutaneous CD30+ T-cell lymphoproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:542" />
        <display value="Primary cutaneous lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:54247" />
        <display value="Posterior cortical atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:54251" />
        <display value="Corticosteroid-sensitive aseptic abscess syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:54260" />
        <display value="Left ventricular noncompaction" />
      </concept>
      <concept>
        <code value="ORPHA:54272" />
        <display value="Hepatocellular adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:543" />
        <display value="Burkitt lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:54368" />
        <display value="Sarcocystosis" />
      </concept>
      <concept>
        <code value="ORPHA:54370" />
        <display value="Primary membranoproliferative glomerulonephritis" />
      </concept>
      <concept>
        <code value="ORPHA:544" />
        <display value="Diffuse large B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:545" />
        <display value="Follicular lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:54595" />
        <display value="Craniopharyngioma" />
      </concept>
      <concept>
        <code value="ORPHA:547" />
        <display value="Non-Hodgkin lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:548" />
        <display value="Leprosy" />
      </concept>
      <concept>
        <code value="ORPHA:549" />
        <display value="Legionellosis" />
      </concept>
      <concept>
        <code value="ORPHA:55" />
        <display value="Oculocutaneous albinism" />
      </concept>
      <concept>
        <code value="ORPHA:550" />
        <display value="MELAS" />
      </concept>
      <concept>
        <code value="ORPHA:551" />
        <display value="MERRF" />
      </concept>
      <concept>
        <code value="ORPHA:552" />
        <display value="MODY" />
      </concept>
      <concept>
        <code value="ORPHA:553" />
        <display value="Cushing syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:55595" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy type 1F" />
      </concept>
      <concept>
        <code value="ORPHA:55596" />
        <display value="Autosomal dominant limb-girdle muscular dystrophy type 1G" />
      </concept>
      <concept>
        <code value="ORPHA:556" />
        <display value="Malakoplakia" />
      </concept>
      <concept>
        <code value="ORPHA:55654" />
        <display value="Hypotrichosis simplex" />
      </concept>
      <concept>
        <code value="ORPHA:55655" />
        <display value="Pneumococcal meningitis" />
      </concept>
      <concept>
        <code value="ORPHA:557" />
        <display value="Isolated anorectal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:558" />
        <display value="Marfan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:55880" />
        <display value="Chondrosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:55881" />
        <display value="Adamantinoma" />
      </concept>
      <concept>
        <code value="ORPHA:559" />
        <display value="Marinesco-Sjogren syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:56" />
        <display value="Alkaptonuria" />
      </concept>
      <concept>
        <code value="ORPHA:560" />
        <display value="Marshall syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:56044" />
        <display value="Carcinoma of gallbladder and extrahepatic biliary tract" />
      </concept>
      <concept>
        <code value="ORPHA:561" />
        <display value="Marshall-Smith syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:562" />
        <display value="McCune-Albright syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:563" />
        <display value="Peripartum cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:56304" />
        <display value="Atelosteogenesis type II" />
      </concept>
      <concept>
        <code value="ORPHA:56305" />
        <display value="Atelosteogenesis type III" />
      </concept>
      <concept>
        <code value="ORPHA:564" />
        <display value="Meckel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:56425" />
        <display value="Cold agglutinin disease" />
      </concept>
      <concept>
        <code value="ORPHA:565" />
        <display value="Menkes disease" />
      </concept>
      <concept>
        <code value="ORPHA:566" />
        <display value="Congenital microcoria" />
      </concept>
      <concept>
        <code value="ORPHA:567" />
        <display value="22q11.2 deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:568" />
        <display value="Microphthalmia, Lenz type" />
      </concept>
      <concept>
        <code value="ORPHA:569" />
        <display value="Familial or sporadic hemiplegic migraine" />
      </concept>
      <concept>
        <code value="ORPHA:56970" />
        <display value="Human prion disease" />
      </concept>
      <concept>
        <code value="ORPHA:57" />
        <display value="Glycogen storage disease due to aldolase A deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:570" />
        <display value="Moebius syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:57145" />
        <display value="SUNCT syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:57146" />
        <display value="Rare hepatic disease" />
      </concept>
      <concept>
        <code value="ORPHA:57196" />
        <display value="Medial condensing osteitis of the clavicle" />
      </concept>
      <concept>
        <code value="ORPHA:572" />
        <display value="Immunodeficiency by defective expression of HLA class 2" />
      </concept>
      <concept>
        <code value="ORPHA:573" />
        <display value="Monilethrix" />
      </concept>
      <concept>
        <code value="ORPHA:574" />
        <display value="Monosomy 21" />
      </concept>
      <concept>
        <code value="ORPHA:575" />
        <display value="Muckle-Wells syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:576" />
        <display value="Mucolipidosis type II" />
      </concept>
      <concept>
        <code value="ORPHA:577" />
        <display value="Mucolipidosis type III" />
      </concept>
      <concept>
        <code value="ORPHA:57777" />
        <display value="Cirrhotic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:57782" />
        <display value="Mazabraud syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:578" />
        <display value="Mucolipidosis type IV" />
      </concept>
      <concept>
        <code value="ORPHA:579" />
        <display value="Mucopolysaccharidosis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:58" />
        <display value="Alexander disease" />
      </concept>
      <concept>
        <code value="ORPHA:580" />
        <display value="Mucopolysaccharidosis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:58017" />
        <display value="Classic hairy cell leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:58040" />
        <display value="Osteoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:581" />
        <display value="Mucopolysaccharidosis type 3" />
      </concept>
      <concept>
        <code value="ORPHA:582" />
        <display value="Mucopolysaccharidosis type 4" />
      </concept>
      <concept>
        <code value="ORPHA:583" />
        <display value="Mucopolysaccharidosis type 6" />
      </concept>
      <concept>
        <code value="ORPHA:584" />
        <display value="Mucopolysaccharidosis type 7" />
      </concept>
      <concept>
        <code value="ORPHA:585" />
        <display value="Multiple sulfatase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:586" />
        <display value="Cystic fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:587" />
        <display value="Muir-Torre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:588" />
        <display value="Muscle-eye-brain disease" />
      </concept>
      <concept>
        <code value="ORPHA:589" />
        <display value="Myasthenia gravis" />
      </concept>
      <concept>
        <code value="ORPHA:59" />
        <display value="Allan-Herndon-Dudley syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:590" />
        <display value="Congenital myasthenic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:591" />
        <display value="Furuncular myiasis" />
      </concept>
      <concept>
        <code value="ORPHA:59135" />
        <display value="Laing early-onset distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:59181" />
        <display value="Sorsby pseudoinflammatory fundus dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:592" />
        <display value="Macrophagic myofasciitis" />
      </concept>
      <concept>
        <code value="ORPHA:59298" />
        <display value="Schilder disease" />
      </concept>
      <concept>
        <code value="ORPHA:593" />
        <display value="Myofibrillar myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:59303" />
        <display value="Neonatal ichthyosis-sclerosing cholangitis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:59305" />
        <display value="Gestational trophoblastic neoplasm" />
      </concept>
      <concept>
        <code value="ORPHA:59306" />
        <display value="McLeod neuroacanthocytosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:59315" />
        <display value="Rhombencephalosynapsis" />
      </concept>
      <concept>
        <code value="ORPHA:595" />
        <display value="Centronuclear myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:596" />
        <display value="X-linked centronuclear myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:597" />
        <display value="Central core disease" />
      </concept>
      <concept>
        <code value="ORPHA:598" />
        <display value="Multiminicore myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:599" />
        <display value="Distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:6" />
        <display value="3-methylcrotonyl-CoA carboxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:60" />
        <display value="Alpha-1-antitrypsin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:600" />
        <display value="Vocal cord and pharyngeal distal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:60014" />
        <display value="Argyria" />
      </concept>
      <concept>
        <code value="ORPHA:60015" />
        <display value="Enlarged parietal foramina" />
      </concept>
      <concept>
        <code value="ORPHA:60025" />
        <display value="Pulmonary alveolar microlithiasis" />
      </concept>
      <concept>
        <code value="ORPHA:60026" />
        <display value="Pulmonary nodular lymphoid hyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:60030" />
        <display value="Loeys-Dietz syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:60032" />
        <display value="Recurrent respiratory papillomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:60033" />
        <display value="Idiopathic bronchiectasis" />
      </concept>
      <concept>
        <code value="ORPHA:60039" />
        <display value="Pudendal neuralgia" />
      </concept>
      <concept>
        <code value="ORPHA:60040" />
        <display value="Megalencephaly-capillary malformation-polymicrogyria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:60041" />
        <display value="Congenital heart block" />
      </concept>
      <concept>
        <code value="ORPHA:602" />
        <display value="GNE myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:603" />
        <display value="Distal myopathy, Welander type" />
      </concept>
      <concept>
        <code value="ORPHA:606" />
        <display value="Proximal myotonic myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:607" />
        <display value="Nemaline myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:609" />
        <display value="Tibial muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:61" />
        <display value="Alpha-mannosidosis" />
      </concept>
      <concept>
        <code value="ORPHA:610" />
        <display value="Bethlem myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:611" />
        <display value="Inclusion body myositis" />
      </concept>
      <concept>
        <code value="ORPHA:612" />
        <display value="Potassium-aggravated myotonia" />
      </concept>
      <concept>
        <code value="ORPHA:614" />
        <display value="Thomsen and Becker disease" />
      </concept>
      <concept>
        <code value="ORPHA:615" />
        <display value="Familial atrial myxoma" />
      </concept>
      <concept>
        <code value="ORPHA:616" />
        <display value="Medulloblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:617" />
        <display value="Congenital primary megaureter" />
      </concept>
      <concept>
        <code value="ORPHA:618" />
        <display value="Familial melanoma" />
      </concept>
      <concept>
        <code value="ORPHA:62" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2D" />
      </concept>
      <concept>
        <code value="ORPHA:620" />
        <display value="Common mesentery" />
      </concept>
      <concept>
        <code value="ORPHA:621" />
        <display value="Hereditary methemoglobinemia" />
      </concept>
      <concept>
        <code value="ORPHA:622" />
        <display value="Homocystinuria without methylmalonic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:624" />
        <display value="Familial multiple nevi flammei" />
      </concept>
      <concept>
        <code value="ORPHA:626" />
        <display value="Large congenital melanocytic nevus" />
      </concept>
      <concept>
        <code value="ORPHA:627" />
        <display value="Nance-Horan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:628" />
        <display value="Diastrophic dwarfism" />
      </concept>
      <concept>
        <code value="ORPHA:629" />
        <display value="Short stature due to growth hormone qualitative anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:63" />
        <display value="Alport syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:631" />
        <display value="Non-acquired isolated growth hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:632" />
        <display value="Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:63259" />
        <display value="Iniencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:63260" />
        <display value="Craniorachischisis" />
      </concept>
      <concept>
        <code value="ORPHA:63273" />
        <display value="Distal myopathy with posterior leg and anterior hand involvement" />
      </concept>
      <concept>
        <code value="ORPHA:63275" />
        <display value="Pemphigoid gestationis" />
      </concept>
      <concept>
        <code value="ORPHA:633" />
        <display value="Laron syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:634" />
        <display value="Netherton syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:63440" />
        <display value="Isolated oxycephaly" />
      </concept>
      <concept>
        <code value="ORPHA:63442" />
        <display value="Angel-shaped phalango-epiphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:63443" />
        <display value="Rare epithelial tumor of stomach" />
      </concept>
      <concept>
        <code value="ORPHA:63446" />
        <display value="Acrocapitofemoral dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:63454" />
        <display value="Pattern dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:63455" />
        <display value="Paraneoplastic pemphigus" />
      </concept>
      <concept>
        <code value="ORPHA:635" />
        <display value="Neuroblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:636" />
        <display value="Neurofibromatosis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:637" />
        <display value="Neurofibromatosis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:638" />
        <display value="Neurofibromatosis-Noonan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:63862" />
        <display value="Schisis association" />
      </concept>
      <concept>
        <code value="ORPHA:639" />
        <display value="Polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG" />
      </concept>
      <concept>
        <code value="ORPHA:63999" />
        <display value="IgG4-related mediastinitis" />
      </concept>
      <concept>
        <code value="ORPHA:64" />
        <display value="Alstrom syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:640" />
        <display value="Hereditary neuropathy with liability to pressure palsies" />
      </concept>
      <concept>
        <code value="ORPHA:641" />
        <display value="Multifocal motor neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:642" />
        <display value="Hereditary sensory and autonomic neuropathy type 4" />
      </concept>
      <concept>
        <code value="ORPHA:64280" />
        <display value="Childhood absence epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:643" />
        <display value="Giant axonal neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:644" />
        <display value="NARP syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:64542" />
        <display value="Acrofacial dysostosis, Kennedy-Teebi type" />
      </concept>
      <concept>
        <code value="ORPHA:64545" />
        <display value="Benign idiopathic neonatal seizures" />
      </concept>
      <concept>
        <code value="ORPHA:646" />
        <display value="Niemann-Pick disease type C" />
      </concept>
      <concept>
        <code value="ORPHA:64686" />
        <display value="Tolosa-Hunt syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:64692" />
        <display value="Oroya fever" />
      </concept>
      <concept>
        <code value="ORPHA:64694" />
        <display value="Trench fever" />
      </concept>
      <concept>
        <code value="ORPHA:647" />
        <display value="Nijmegen breakage syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:64720" />
        <display value="Leiomyosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:64722" />
        <display value="Granulomatous mastitis" />
      </concept>
      <concept>
        <code value="ORPHA:64734" />
        <display value="Iridocorneal endothelial syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:64739" />
        <display value="Ovarian hyperstimulation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:64740" />
        <display value="Recurrent acute pancreatitis" />
      </concept>
      <concept>
        <code value="ORPHA:64741" />
        <display value="Pulmonary blastoma" />
      </concept>
      <concept>
        <code value="ORPHA:64742" />
        <display value="Pleuropulmonary blastoma" />
      </concept>
      <concept>
        <code value="ORPHA:64743" />
        <display value="Hepatoportal sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:64744" />
        <display value="IgG4-related thyroid disease" />
      </concept>
      <concept>
        <code value="ORPHA:64745" />
        <display value="Pruritic urticarial papules and plaques of pregnancy" />
      </concept>
      <concept>
        <code value="ORPHA:64746" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2" />
      </concept>
      <concept>
        <code value="ORPHA:64747" />
        <display value="X-linked Charcot-Marie-Tooth disease" />
      </concept>
      <concept>
        <code value="ORPHA:64748" />
        <display value="Dejerine-Sottas syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:64749" />
        <display value="Charcot-Marie-Tooth disease type 4" />
      </concept>
      <concept>
        <code value="ORPHA:64751" />
        <display value="Hereditary motor and sensory neuropathy type 5" />
      </concept>
      <concept>
        <code value="ORPHA:64752" />
        <display value="Hereditary sensory and autonomic neuropathy type 5" />
      </concept>
      <concept>
        <code value="ORPHA:64753" />
        <display value="Spinocerebellar ataxia with axonal neuropathy type 2" />
      </concept>
      <concept>
        <code value="ORPHA:64754" />
        <display value="Nevus comedonicus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:64755" />
        <display value="Becker nevus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:648" />
        <display value="Noonan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:649" />
        <display value="Norrie disease" />
      </concept>
      <concept>
        <code value="ORPHA:65" />
        <display value="Leber congenital amaurosis" />
      </concept>
      <concept>
        <code value="ORPHA:650" />
        <display value="LCAT deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:652" />
        <display value="Multiple endocrine neoplasia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:65250" />
        <display value="Perineural cyst" />
      </concept>
      <concept>
        <code value="ORPHA:65282" />
        <display value="Carvajal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:65283" />
        <display value="Timothy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:65284" />
        <display value="Biotin-thiamine-responsive basal ganglia disease" />
      </concept>
      <concept>
        <code value="ORPHA:65285" />
        <display value="Lhermitte-Duclos disease" />
      </concept>
      <concept>
        <code value="ORPHA:65286" />
        <display value="3q29 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:65287" />
        <display value="Beta-ureidopropionase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:65288" />
        <display value="Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:653" />
        <display value="Multiple endocrine neoplasia type 2" />
      </concept>
      <concept>
        <code value="ORPHA:654" />
        <display value="Nephroblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:655" />
        <display value="Nephronophthisis" />
      </concept>
      <concept>
        <code value="ORPHA:656" />
        <display value="Familial idiopathic steroid-resistant nephrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:65681" />
        <display value="Vaginal atresia" />
      </concept>
      <concept>
        <code value="ORPHA:65682" />
        <display value="Benign recurrent intrahepatic cholestasis" />
      </concept>
      <concept>
        <code value="ORPHA:65683" />
        <display value="Isolated focal cortical dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:65684" />
        <display value="Monomelic amyotrophy" />
      </concept>
      <concept>
        <code value="ORPHA:657" />
        <display value="Congenital isolated hyperinsulinism" />
      </concept>
      <concept>
        <code value="ORPHA:65720" />
        <display value="Arthrogryposis-severe scoliosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:65743" />
        <display value="Autosomal dominant multiple pterygium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:65748" />
        <display value="Multiple self-healing squamous epithelioma" />
      </concept>
      <concept>
        <code value="ORPHA:65753" />
        <display value="Charcot-Marie-Tooth disease type 1" />
      </concept>
      <concept>
        <code value="ORPHA:65759" />
        <display value="Carpenter syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:65798" />
        <display value="Goodman syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:658" />
        <display value="Non-histaminic angioedema" />
      </concept>
      <concept>
        <code value="ORPHA:659" />
        <display value="Mutilating palmoplantar keratoderma with periorificial keratotic plaques" />
      </concept>
      <concept>
        <code value="ORPHA:660" />
        <display value="Omphalocele" />
      </concept>
      <concept>
        <code value="ORPHA:661" />
        <display value="Ondine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:662" />
        <display value="Yellow nail syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:663" />
        <display value="Mitochondrial DNA-related progressive external ophthalmoplegia" />
      </concept>
      <concept>
        <code value="ORPHA:664" />
        <display value="Ornithine transcarbamylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:66518" />
        <display value="Short fifth metacarpals-insulin resistance syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:66529" />
        <display value="Tako-Tsubo cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:666" />
        <display value="Osteogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:66624" />
        <display value="PANDAS" />
      </concept>
      <concept>
        <code value="ORPHA:66625" />
        <display value="Cerebrooculonasal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:66627" />
        <display value="Pigmented villonodular synovitis" />
      </concept>
      <concept>
        <code value="ORPHA:66628" />
        <display value="Obesity due to congenital leptin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:66629" />
        <display value="Goldberg-Shprintzen megacolon syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:66630" />
        <display value="Congenital pseudoarthrosis of the clavicle" />
      </concept>
      <concept>
        <code value="ORPHA:66631" />
        <display value="CEDNIK syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:66633" />
        <display value="Sensorineural hearing loss-early graying-essential tremor syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:66634" />
        <display value="Dilated cardiomyopathy with ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:66637" />
        <display value="Diaphanospondylodysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:66646" />
        <display value="Cutaneous mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:66661" />
        <display value="Mast cell sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:66662" />
        <display value="Extracutaneous mastocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:667" />
        <display value="Autosomal recessive malignant osteopetrosis" />
      </concept>
      <concept>
        <code value="ORPHA:668" />
        <display value="Osteosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:67" />
        <display value="Amoebiasis due to Entamoeba histolytica" />
      </concept>
      <concept>
        <code value="ORPHA:67036" />
        <display value="Autosomal dominant optic atrophy and cataract" />
      </concept>
      <concept>
        <code value="ORPHA:67038" />
        <display value="B-cell chronic lymphocytic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:67039" />
        <display value="Segmental odontomaxillary dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:67041" />
        <display value="Hyaluronidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:67042" />
        <display value="Late-onset retinal degeneration" />
      </concept>
      <concept>
        <code value="ORPHA:67043" />
        <display value="Acanthamoeba keratitis" />
      </concept>
      <concept>
        <code value="ORPHA:67044" />
        <display value="Thrombocytopenia with congenital dyserythropoietic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:67045" />
        <display value="X-linked intellectual disability with isolated growth hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:67046" />
        <display value="3-methylglutaconic aciduria type 1" />
      </concept>
      <concept>
        <code value="ORPHA:67047" />
        <display value="3-methylglutaconic aciduria type 3" />
      </concept>
      <concept>
        <code value="ORPHA:67048" />
        <display value="3-methylglutaconic aciduria type 4" />
      </concept>
      <concept>
        <code value="ORPHA:671" />
        <display value="Primary cutis verticis gyrata" />
      </concept>
      <concept>
        <code value="ORPHA:672" />
        <display value="Pallister-Hall syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:673" />
        <display value="Malaria" />
      </concept>
      <concept>
        <code value="ORPHA:674" />
        <display value="Accessory pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:675" />
        <display value="Annular pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:676" />
        <display value="Hereditary chronic pancreatitis" />
      </concept>
      <concept>
        <code value="ORPHA:677" />
        <display value="Pancreatoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:678" />
        <display value="Papillon-Lefavre syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:679" />
        <display value="Malignant atrophic papulosis" />
      </concept>
      <concept>
        <code value="ORPHA:68" />
        <display value="Amoebiasis due to free-living amoebae" />
      </concept>
      <concept>
        <code value="ORPHA:681" />
        <display value="Hypokalemic periodic paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:682" />
        <display value="Hyperkalemic periodic paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:683" />
        <display value="Progressive supranuclear palsy" />
      </concept>
      <concept>
        <code value="ORPHA:68329" />
        <display value="Rare maxillo-facial surgical disease" />
      </concept>
      <concept>
        <code value="ORPHA:68334" />
        <display value="Rare hemorrhagic disorder due to a constitutional coagulation factors defect" />
      </concept>
      <concept>
        <code value="ORPHA:68335" />
        <display value="Chromosomal anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:68336" />
        <display value="Rare genetic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:68341" />
        <display value="Multiple congenital anomalies/dysmorphic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:68346" />
        <display value="Rare genetic skin disease" />
      </concept>
      <concept>
        <code value="ORPHA:68347" />
        <display value="Tumor of hematopoietic and lymphoid tissues" />
      </concept>
      <concept>
        <code value="ORPHA:68354" />
        <display value="Sleep disorder" />
      </concept>
      <concept>
        <code value="ORPHA:68356" />
        <display value="Leukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:68361" />
        <display value="Rare deafness" />
      </concept>
      <concept>
        <code value="ORPHA:68362" />
        <display value="Rare vascular disease" />
      </concept>
      <concept>
        <code value="ORPHA:68363" />
        <display value="Rare dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:68364" />
        <display value="Hemoglobinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:68366" />
        <display value="Lysosomal disease" />
      </concept>
      <concept>
        <code value="ORPHA:68367" />
        <display value="Rare inborn errors of metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:68373" />
        <display value="Peroxisomal disease" />
      </concept>
      <concept>
        <code value="ORPHA:68378" />
        <display value="Congenital limb malformation" />
      </concept>
      <concept>
        <code value="ORPHA:68380" />
        <display value="Mitochondrial disease" />
      </concept>
      <concept>
        <code value="ORPHA:68381" />
        <display value="Neuromuscular disease" />
      </concept>
      <concept>
        <code value="ORPHA:68383" />
        <display value="Rare constitutional aplastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:68385" />
        <display value="Neurometabolic disease" />
      </concept>
      <concept>
        <code value="ORPHA:684" />
        <display value="Paramyotonia congenita of Von Eulenburg" />
      </concept>
      <concept>
        <code value="ORPHA:68402" />
        <display value="Rare parkinsonian disorder" />
      </concept>
      <concept>
        <code value="ORPHA:68411" />
        <display value="Rare bone tumor" />
      </concept>
      <concept>
        <code value="ORPHA:68415" />
        <display value="Rare parathyroid disease and phosphocalcic metabolism anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:68416" />
        <display value="Rare infectious disease" />
      </concept>
      <concept>
        <code value="ORPHA:68419" />
        <display value="Vascular anomaly or angioma" />
      </concept>
      <concept>
        <code value="ORPHA:685" />
        <display value="Hereditary spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:69" />
        <display value="Amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:69028" />
        <display value="Dysostosis with brachydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:69061" />
        <display value="Idiopathic steroid-sensitive nephrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69063" />
        <display value="Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization" />
      </concept>
      <concept>
        <code value="ORPHA:69076" />
        <display value="Familial renal glucosuria" />
      </concept>
      <concept>
        <code value="ORPHA:69077" />
        <display value="Rhabdoid tumor" />
      </concept>
      <concept>
        <code value="ORPHA:69078" />
        <display value="Liposarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:69082" />
        <display value="Odonto-tricho-ungual-digito-palmar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69083" />
        <display value="Ectodermal dysplasia with natal teeth, Turnpenny type" />
      </concept>
      <concept>
        <code value="ORPHA:69084" />
        <display value="Pure hair and nail ectodermal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:69085" />
        <display value="Limb-mammary syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69087" />
        <display value="Naegeli-Franceschetti-Jadassohn syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69088" />
        <display value="Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69125" />
        <display value="Anonychia with flexural pigmentation" />
      </concept>
      <concept>
        <code value="ORPHA:69126" />
        <display value="Pyogenic arthritis-pyoderma gangrenosum-acne syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69663" />
        <display value="Low phospholipid associated cholelithiasis" />
      </concept>
      <concept>
        <code value="ORPHA:69665" />
        <display value="Intrahepatic cholestasis of pregnancy" />
      </concept>
      <concept>
        <code value="ORPHA:69723" />
        <display value="Tyrosinemia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:69735" />
        <display value="Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69736" />
        <display value="Bilateral acute depigmentation of the iris" />
      </concept>
      <concept>
        <code value="ORPHA:69737" />
        <display value="Bosley-Salih-Alorainy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69739" />
        <display value="Athabaskan brainstem dysgenesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:69744" />
        <display value="Circumscribed palmoplantar hypokeratosis" />
      </concept>
      <concept>
        <code value="ORPHA:69745" />
        <display value="Warty dyskeratoma" />
      </concept>
      <concept>
        <code value="ORPHA:699" />
        <display value="Pearson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:7" />
        <display value="3C syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:70" />
        <display value="Proximal spinal muscular atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:700" />
        <display value="Alopecia totalis" />
      </concept>
      <concept>
        <code value="ORPHA:701" />
        <display value="Alopecia universalis" />
      </concept>
      <concept>
        <code value="ORPHA:702" />
        <display value="Pelizaeus-Merzbacher disease" />
      </concept>
      <concept>
        <code value="ORPHA:703" />
        <display value="Bullous pemphigoid" />
      </concept>
      <concept>
        <code value="ORPHA:704" />
        <display value="Pemphigus vulgaris" />
      </concept>
      <concept>
        <code value="ORPHA:70470" />
        <display value="Hyperlipoproteinemia type 5" />
      </concept>
      <concept>
        <code value="ORPHA:70472" />
        <display value="Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type" />
      </concept>
      <concept>
        <code value="ORPHA:70474" />
        <display value="Leigh syndrome with cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:70475" />
        <display value="Radiation proctitis" />
      </concept>
      <concept>
        <code value="ORPHA:70476" />
        <display value="Vernal keratoconjunctivitis" />
      </concept>
      <concept>
        <code value="ORPHA:70482" />
        <display value="Carcinoma of esophagus" />
      </concept>
      <concept>
        <code value="ORPHA:705" />
        <display value="Pendred syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:70567" />
        <display value="Cholangiocarcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:70568" />
        <display value="Post-transplant lymphoproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:70573" />
        <display value="Small cell lung cancer" />
      </concept>
      <concept>
        <code value="ORPHA:70578" />
        <display value="Adult acute respiratory distress syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:70587" />
        <display value="Infant acute respiratory distress syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:70588" />
        <display value="Meconium aspiration syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:70589" />
        <display value="Bronchopulmonary dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:70590" />
        <display value="Infantile apnea" />
      </concept>
      <concept>
        <code value="ORPHA:70591" />
        <display value="Chronic thromboembolic pulmonary hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:70592" />
        <display value="Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:70593" />
        <display value="Immunodeficiency due to selective anti-polysaccharide antibody deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:70594" />
        <display value="Dopa-responsive dystonia due to sepiapterin reductase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:70595" />
        <display value="Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:70596" />
        <display value="Congenital Epstein-Barr virus infection" />
      </concept>
      <concept>
        <code value="ORPHA:707" />
        <display value="Plague" />
      </concept>
      <concept>
        <code value="ORPHA:708" />
        <display value="Peters anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:709" />
        <display value="Peters plus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71" />
        <display value="Chylomicron retention disease" />
      </concept>
      <concept>
        <code value="ORPHA:710" />
        <display value="Pfeiffer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71198" />
        <display value="Rare pulmonary hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:712" />
        <display value="Hemolytic anemia due to glucophosphate isomerase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:71202" />
        <display value="Rare hemorrhagic disorder due to a constitutional platelet anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:71203" />
        <display value="Autoimmune thrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:71209" />
        <display value="Rare soft tissue tumor" />
      </concept>
      <concept>
        <code value="ORPHA:71211" />
        <display value="Neuromyelitis optica" />
      </concept>
      <concept>
        <code value="ORPHA:71212" />
        <display value="Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:71213" />
        <display value="Retinal capillary malformation" />
      </concept>
      <concept>
        <code value="ORPHA:71267" />
        <display value="Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71271" />
        <display value="Split hand-split foot-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71272" />
        <display value="Sandifer syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71273" />
        <display value="Renal nutcracker syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71274" />
        <display value="Disseminated peritoneal leiomyomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:71275" />
        <display value="Rh deficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71276" />
        <display value="Silent sinus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71277" />
        <display value="Encephalopathy due to GLUT1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:71278" />
        <display value="Congenital brain dysgenesis due to glutamine synthetase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:71279" />
        <display value="CANOMAD syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71281" />
        <display value="Rare central nervous system and retinal vascular disease" />
      </concept>
      <concept>
        <code value="ORPHA:71289" />
        <display value="Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71290" />
        <display value="Hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:713" />
        <display value="Glycogen storage disease due to phosphoglycerate kinase 1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:714" />
        <display value="Hemolytic anemia due to diphosphoglycerate mutase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:71493" />
        <display value="Familial thrombocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:715" />
        <display value="Glycogen storage disease due to muscle phosphorylase kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:71505" />
        <display value="Cancer-associated retinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:71517" />
        <display value="Rapid-onset dystonia-parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:71518" />
        <display value="Benign paroxysmal torticollis of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:71519" />
        <display value="Psychogenic movement disorders" />
      </concept>
      <concept>
        <code value="ORPHA:71526" />
        <display value="Obesity due to pro-opiomelanocortin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:71528" />
        <display value="Obesity due to prohormone convertase I deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:71529" />
        <display value="Obesity due to melanocortin 4 receptor deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:716" />
        <display value="Phenylketonuria" />
      </concept>
      <concept>
        <code value="ORPHA:717" />
        <display value="Catecholamine-producing tumor" />
      </concept>
      <concept>
        <code value="ORPHA:718" />
        <display value="Isolated Pierre Robin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:71859" />
        <display value="Rare genetic neurological disorder" />
      </concept>
      <concept>
        <code value="ORPHA:71862" />
        <display value="Inherited retinal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:71864" />
        <display value="Muscular channelopathy" />
      </concept>
      <concept>
        <code value="ORPHA:72" />
        <display value="Angelman syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:720" />
        <display value="Pili bifurcati" />
      </concept>
      <concept>
        <code value="ORPHA:721" />
        <display value="Gray platelet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:722" />
        <display value="Hypoplasminogenemia" />
      </concept>
      <concept>
        <code value="ORPHA:723" />
        <display value="Pneumocystosis" />
      </concept>
      <concept>
        <code value="ORPHA:724" />
        <display value="Idiopathic acute eosinophilic pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:725" />
        <display value="Continuous spikes and waves during sleep" />
      </concept>
      <concept>
        <code value="ORPHA:726" />
        <display value="Alpers-Huttenlocher syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:727" />
        <display value="Microscopic polyangiitis" />
      </concept>
      <concept>
        <code value="ORPHA:728" />
        <display value="Relapsing polychondritis" />
      </concept>
      <concept>
        <code value="ORPHA:729" />
        <display value="Polycythemia vera" />
      </concept>
      <concept>
        <code value="ORPHA:73" />
        <display value="Gorham-Stout disease" />
      </concept>
      <concept>
        <code value="ORPHA:730" />
        <display value="Autosomal dominant polycystic kidney disease" />
      </concept>
      <concept>
        <code value="ORPHA:73014" />
        <display value="Intractable diarrhea of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:731" />
        <display value="Autosomal recessive polycystic kidney disease" />
      </concept>
      <concept>
        <code value="ORPHA:732" />
        <display value="Polymyositis" />
      </concept>
      <concept>
        <code value="ORPHA:73217" />
        <display value="Mullerian aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:73220" />
        <display value="X-linked intellectual disability-hypotonic face syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:73223" />
        <display value="Global developmental delay-osteopenia-ectodermal defect syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:73224" />
        <display value="Tubular renal disease-cardiomyopathy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:73229" />
        <display value="HANAC syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:73230" />
        <display value="Ossification anomalies-psychomotor developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:73245" />
        <display value="Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:73246" />
        <display value="Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:73247" />
        <display value="Eosinophilic esophagitis" />
      </concept>
      <concept>
        <code value="ORPHA:73256" />
        <display value="Central neurocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:73260" />
        <display value="Paracoccidioidomycosis" />
      </concept>
      <concept>
        <code value="ORPHA:73263" />
        <display value="Zygomycosis" />
      </concept>
      <concept>
        <code value="ORPHA:73267" />
        <display value="Non-24-hour sleep-wake syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:73271" />
        <display value="Bleeding diathesis due to a collagen receptor defect" />
      </concept>
      <concept>
        <code value="ORPHA:73272" />
        <display value="Growth delay due to insulin-like growth factor type 1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:73273" />
        <display value="Growth delay due to insulin-like growth factor I resistance" />
      </concept>
      <concept>
        <code value="ORPHA:73274" />
        <display value="Acquired hemophilia" />
      </concept>
      <concept>
        <code value="ORPHA:733" />
        <display value="Familial adenomatous polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:734" />
        <display value="Alpha delta granule deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:73423" />
        <display value="Acute ackee fruit intoxication" />
      </concept>
      <concept>
        <code value="ORPHA:735" />
        <display value="Porokeratosis of Mibelli" />
      </concept>
      <concept>
        <code value="ORPHA:737" />
        <display value="Porokeratosis plantaris palmaris et disseminata" />
      </concept>
      <concept>
        <code value="ORPHA:738" />
        <display value="Porphyria" />
      </concept>
      <concept>
        <code value="ORPHA:739" />
        <display value="Prader-Willi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:74" />
        <display value="Angiostrongyliasis" />
      </concept>
      <concept>
        <code value="ORPHA:740" />
        <display value="Hutchinson-Gilford progeria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:741" />
        <display value="Familial mitral valve prolapse" />
      </concept>
      <concept>
        <code value="ORPHA:742" />
        <display value="Prolidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:743" />
        <display value="Severe hereditary thrombophilia due to congenital protein S deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:744" />
        <display value="Proteus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:745" />
        <display value="Severe hereditary thrombophilia due to congenital protein C deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:746" />
        <display value="Mitochondrial trifunctional protein deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:747" />
        <display value="Autoimmune pulmonary alveolar proteinosis" />
      </concept>
      <concept>
        <code value="ORPHA:748" />
        <display value="Mendelian susceptibility to mycobacterial diseases" />
      </concept>
      <concept>
        <code value="ORPHA:749" />
        <display value="Congenital prekallikrein deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:750" />
        <display value="Pseudoachondroplasia" />
      </concept>
      <concept>
        <code value="ORPHA:75110" />
        <display value="Myiasis" />
      </concept>
      <concept>
        <code value="ORPHA:752" />
        <display value="46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:75233" />
        <display value="Wolman disease" />
      </concept>
      <concept>
        <code value="ORPHA:75234" />
        <display value="Cholesteryl ester storage disease" />
      </concept>
      <concept>
        <code value="ORPHA:75249" />
        <display value="Familial isolated restrictive cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:753" />
        <display value="46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:75325" />
        <display value="Osteosclerosis-ichthyosis-premature ovarian failure syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:75326" />
        <display value="Retinal arterial tortuosity" />
      </concept>
      <concept>
        <code value="ORPHA:75327" />
        <display value="North Carolina macular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:75373" />
        <display value="Progressive bifocal chorioretinal atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:75374" />
        <display value="Bradyopsia" />
      </concept>
      <concept>
        <code value="ORPHA:75376" />
        <display value="Familial drusen" />
      </concept>
      <concept>
        <code value="ORPHA:75377" />
        <display value="Central areolar choroidal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:75378" />
        <display value="Oligocone trichromacy" />
      </concept>
      <concept>
        <code value="ORPHA:75381" />
        <display value="Cystoid macular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:75382" />
        <display value="Oguchi disease" />
      </concept>
      <concept>
        <code value="ORPHA:75389" />
        <display value="Brain malformation-congenital heart disease-postaxial polydactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:75391" />
        <display value="Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:75392" />
        <display value="Ehlers-Danlos syndrome, periodontitis type" />
      </concept>
      <concept>
        <code value="ORPHA:754" />
        <display value="Androgen insensitivity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:75496" />
        <display value="Ehlers-Danlos syndrome, progeroid type" />
      </concept>
      <concept>
        <code value="ORPHA:75497" />
        <display value="X-linked Ehlers-Danlos syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:755" />
        <display value="Leydig cell hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:75501" />
        <display value="Ehlers-Danlos syndrome, fibronectinemic type" />
      </concept>
      <concept>
        <code value="ORPHA:75508" />
        <display value="Angioosteohypotrophic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:75563" />
        <display value="X-linked sideroblastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:75564" />
        <display value="Acquired idiopathic sideroblastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:75565" />
        <display value="Tropical endomyocardial fibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:75566" />
        <display value="Loeffler endocarditis" />
      </concept>
      <concept>
        <code value="ORPHA:75567" />
        <display value="Primary progressive freezing gait" />
      </concept>
      <concept>
        <code value="ORPHA:756" />
        <display value="Pseudohypoaldosteronism type 1" />
      </concept>
      <concept>
        <code value="ORPHA:757" />
        <display value="Pseudohypoaldosteronism type 2" />
      </concept>
      <concept>
        <code value="ORPHA:758" />
        <display value="Pseudoxanthoma elasticum" />
      </concept>
      <concept>
        <code value="ORPHA:75840" />
        <display value="Congenital muscular dystrophy, Ullrich type" />
      </concept>
      <concept>
        <code value="ORPHA:75857" />
        <display value="6q terminal deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:75858" />
        <display value="MORM syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:759" />
        <display value="Central precocious puberty" />
      </concept>
      <concept>
        <code value="ORPHA:76" />
        <display value="Strongyloidiasis" />
      </concept>
      <concept>
        <code value="ORPHA:760" />
        <display value="Purine nucleoside phosphorylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:761" />
        <display value="Immunoglobulin A vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:763" />
        <display value="Pycnodysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:764" />
        <display value="Pyomyositis" />
      </concept>
      <concept>
        <code value="ORPHA:765" />
        <display value="Pyruvate dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:766" />
        <display value="Hemolytic anemia due to red cell pyruvate kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:767" />
        <display value="Polyarteritis nodosa" />
      </concept>
      <concept>
        <code value="ORPHA:768" />
        <display value="Familial long QT syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:769" />
        <display value="Rabson-Mendenhall syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:770" />
        <display value="Rabies" />
      </concept>
      <concept>
        <code value="ORPHA:772" />
        <display value="Infantile Refsum disease" />
      </concept>
      <concept>
        <code value="ORPHA:77240" />
        <display value="Primary lymphedema" />
      </concept>
      <concept>
        <code value="ORPHA:77243" />
        <display value="Lipedema" />
      </concept>
      <concept>
        <code value="ORPHA:77258" />
        <display value="Trichorhinophalangeal syndrome type 1 and 3" />
      </concept>
      <concept>
        <code value="ORPHA:77259" />
        <display value="Gaucher disease type 1" />
      </concept>
      <concept>
        <code value="ORPHA:77260" />
        <display value="Gaucher disease type 2" />
      </concept>
      <concept>
        <code value="ORPHA:77261" />
        <display value="Gaucher disease type 3" />
      </concept>
      <concept>
        <code value="ORPHA:77292" />
        <display value="Niemann-Pick disease type A" />
      </concept>
      <concept>
        <code value="ORPHA:77293" />
        <display value="Niemann-Pick disease type B" />
      </concept>
      <concept>
        <code value="ORPHA:77295" />
        <display value="Odontoleukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:77296" />
        <display value="Morgagni-Stewart-Morel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:77297" />
        <display value="Majeed syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:77298" />
        <display value="Anophthalmia/microphthalmia-esophageal atresia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:77299" />
        <display value="Microphthalmia-brain atrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:773" />
        <display value="Refsum disease" />
      </concept>
      <concept>
        <code value="ORPHA:77300" />
        <display value="Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:77301" />
        <display value="Monosomy 9q22.3" />
      </concept>
      <concept>
        <code value="ORPHA:774" />
        <display value="Hereditary hemorrhagic telangiectasia" />
      </concept>
      <concept>
        <code value="ORPHA:776" />
        <display value="X-linked intellectual disability with marfanoid habitus" />
      </concept>
      <concept>
        <code value="ORPHA:777" />
        <display value="X-linked non-syndromic intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:778" />
        <display value="Rett syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:77828" />
        <display value="Genetic obesity" />
      </concept>
      <concept>
        <code value="ORPHA:77830" />
        <display value="Rare genetic odontologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:779" />
        <display value="Reynolds syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:78" />
        <display value="Ankylostomiasis" />
      </concept>
      <concept>
        <code value="ORPHA:780" />
        <display value="Rhabdomyosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:781" />
        <display value="Q fever" />
      </concept>
      <concept>
        <code value="ORPHA:782" />
        <display value="Axenfeld-Rieger syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:783" />
        <display value="Rubinstein-Taybi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:785" />
        <display value="Estrogen resistance syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:786" />
        <display value="Glucocorticoid resistance" />
      </concept>
      <concept>
        <code value="ORPHA:79" />
        <display value="Congenital alpha2-antiplasmin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:790" />
        <display value="Retinoblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:79062" />
        <display value="Disorder of amino acid and other organic acid metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79076" />
        <display value="Juvenile polyposis of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:79078" />
        <display value="IgG4-related dacryoadenitis and sialadenitis" />
      </concept>
      <concept>
        <code value="ORPHA:79083" />
        <display value="PPARG-related familial partial lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:79084" />
        <display value="Familial partial lipodystrophy, Kobberling type" />
      </concept>
      <concept>
        <code value="ORPHA:79085" />
        <display value="AKT2-related familial partial lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:79086" />
        <display value="Acquired generalized lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:79087" />
        <display value="Acquired partial lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:79088" />
        <display value="Localized lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:79091" />
        <display value="Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79093" />
        <display value="Foix-Alajouanine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79094" />
        <display value="Grange syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79095" />
        <display value="Congenital bile acid synthesis defect type 4" />
      </concept>
      <concept>
        <code value="ORPHA:79096" />
        <display value="Pyridoxal phosphate-responsive seizures" />
      </concept>
      <concept>
        <code value="ORPHA:79097" />
        <display value="Folinic acid-responsive seizures" />
      </concept>
      <concept>
        <code value="ORPHA:79098" />
        <display value="Sympathetic ophthalmia" />
      </concept>
      <concept>
        <code value="ORPHA:79099" />
        <display value="Interstitial granulomatous dermatitis with arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:791" />
        <display value="Retinitis pigmentosa" />
      </concept>
      <concept>
        <code value="ORPHA:79100" />
        <display value="Atrophoderma vermiculata" />
      </concept>
      <concept>
        <code value="ORPHA:79101" />
        <display value="Hyperprolinemia type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79102" />
        <display value="Thyrotoxic periodic paralysis" />
      </concept>
      <concept>
        <code value="ORPHA:79105" />
        <display value="Myxofibrosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:79106" />
        <display value="Eiken syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79107" />
        <display value="Developmental malformations-deafness-dystonia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79113" />
        <display value="Mandibulofacial dysostosis-microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79118" />
        <display value="Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79124" />
        <display value="Hepatic veno-occlusive disease-immunodeficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79126" />
        <display value="Acute interstitial pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:79127" />
        <display value="Respiratory bronchiolitis-interstitial lung disease syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79128" />
        <display value="Lymphoid interstitial pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:79129" />
        <display value="Trichodysplasia-amelogenesis imperfecta syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79132" />
        <display value="Sparse hair-short stature-skin anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79133" />
        <display value="Focal facial dermal dysplasia type I" />
      </concept>
      <concept>
        <code value="ORPHA:79134" />
        <display value="DEND syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79135" />
        <display value="Episodic ataxia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:79136" />
        <display value="Episodic ataxia type 4" />
      </concept>
      <concept>
        <code value="ORPHA:79137" />
        <display value="Generalized epilepsy-paroxysmal dyskinesia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79138" />
        <display value="Bickerstaff brainstem encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:79139" />
        <display value="Japanese encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:79140" />
        <display value="Cutaneous neuroendocrine carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:79141" />
        <display value="Hereditary painful callosities" />
      </concept>
      <concept>
        <code value="ORPHA:79143" />
        <display value="Isolated congenital anonychia" />
      </concept>
      <concept>
        <code value="ORPHA:79144" />
        <display value="Isolated congenital onychodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:79145" />
        <display value="Dowling-Degos disease" />
      </concept>
      <concept>
        <code value="ORPHA:79146" />
        <display value="Familial progressive hyperpigmentation" />
      </concept>
      <concept>
        <code value="ORPHA:79147" />
        <display value="Familial reactive perforating collagenosis" />
      </concept>
      <concept>
        <code value="ORPHA:79148" />
        <display value="Elastosis perforans serpiginosa" />
      </concept>
      <concept>
        <code value="ORPHA:79149" />
        <display value="Dermochondrocorneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:79150" />
        <display value="Linear and whorled nevoid hypermelanosis" />
      </concept>
      <concept>
        <code value="ORPHA:79151" />
        <display value="Acrokeratosis verruciformis of Hopf" />
      </concept>
      <concept>
        <code value="ORPHA:79152" />
        <display value="Disseminated superficial actinic porokeratosis" />
      </concept>
      <concept>
        <code value="ORPHA:79153" />
        <display value="Idiopathic trachyonychia" />
      </concept>
      <concept>
        <code value="ORPHA:79154" />
        <display value="2-aminoadipic 2-oxoadipic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:79155" />
        <display value="Encephalopathy due to hydroxykynureninuria" />
      </concept>
      <concept>
        <code value="ORPHA:79156" />
        <display value="Seizures-intellectual disability due to hydroxylysinuria syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79157" />
        <display value="2-methylbutyryl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79158" />
        <display value="Cerebral organic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:79159" />
        <display value="Isobutyryl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79161" />
        <display value="Disorder of carbohydrate metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79163" />
        <display value="Classic organic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:79166" />
        <display value="Disorder of amino acid absorption and transport" />
      </concept>
      <concept>
        <code value="ORPHA:79167" />
        <display value="Disorder of urea cycle metabolism and ammonia detoxification" />
      </concept>
      <concept>
        <code value="ORPHA:79168" />
        <display value="Disorder of bile acid synthesis" />
      </concept>
      <concept>
        <code value="ORPHA:79169" />
        <display value="Disorder of neurotransmitter metabolism and transport" />
      </concept>
      <concept>
        <code value="ORPHA:79171" />
        <display value="Disorder of cobalamin metabolism and transport" />
      </concept>
      <concept>
        <code value="ORPHA:79172" />
        <display value="Creatine deficiency syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79173" />
        <display value="Disorder of methionine cycle and sulfur amino acid metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79174" />
        <display value="Disorder of fatty acid oxidation and ketone body metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79175" />
        <display value="Disorder of gamma-aminobutyric acid metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79177" />
        <display value="Gluconeogenesis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79178" />
        <display value="Glucose transport disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79179" />
        <display value="Disorder of glycerol metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79181" />
        <display value="Disorder of histidine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79183" />
        <display value="Disorder of ketolysis" />
      </concept>
      <concept>
        <code value="ORPHA:79185" />
        <display value="Disorder of ornithine or proline metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79186" />
        <display value="Disorder of pentose phosphate metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79187" />
        <display value="Disorder of peptide metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79188" />
        <display value="Peroxisomal beta-oxidation disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79189" />
        <display value="Peroxisome biogenesis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79190" />
        <display value="Disorder of phenylalanin or tyrosine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79191" />
        <display value="Disorder of purine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79192" />
        <display value="Disorder of pyridoxine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79193" />
        <display value="Disorder of pyrimidine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79194" />
        <display value="Disorder of serine or glycine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79195" />
        <display value="Sterol biosynthesis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79196" />
        <display value="Disorder of the gamma-glutamyl cycle" />
      </concept>
      <concept>
        <code value="ORPHA:79197" />
        <display value="Disorder of branched-chain amino acid metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:792" />
        <display value="X-linked retinoschisis" />
      </concept>
      <concept>
        <code value="ORPHA:79200" />
        <display value="Disorder of energy metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79201" />
        <display value="Glycogen storage disease" />
      </concept>
      <concept>
        <code value="ORPHA:79204" />
        <display value="Lipid storage disease" />
      </concept>
      <concept>
        <code value="ORPHA:79207" />
        <display value="Disorder of lysosomal amino acid transport" />
      </concept>
      <concept>
        <code value="ORPHA:79211" />
        <display value="Combined hyperlipidemia" />
      </concept>
      <concept>
        <code value="ORPHA:79212" />
        <display value="Mucolipidosis" />
      </concept>
      <concept>
        <code value="ORPHA:79213" />
        <display value="Mucopolysaccharidosis" />
      </concept>
      <concept>
        <code value="ORPHA:79214" />
        <display value="Disorder of biogenic amine metabolism and transport" />
      </concept>
      <concept>
        <code value="ORPHA:79215" />
        <display value="Oligosaccharidosis" />
      </concept>
      <concept>
        <code value="ORPHA:79217" />
        <display value="Other metabolic disease with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:79219" />
        <display value="Metabolic disease involving other neurotransmitter deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79224" />
        <display value="Disorder of purine or pyrimidine metabolism" />
      </concept>
      <concept>
        <code value="ORPHA:79225" />
        <display value="Sphingolipidosis" />
      </concept>
      <concept>
        <code value="ORPHA:79226" />
        <display value="Sterol metabolism disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79230" />
        <display value="Hemochromatosis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79233" />
        <display value="Hypoxanthine guanine phosphoribosyltransferase partial deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79234" />
        <display value="Crigler-Najjar syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:79235" />
        <display value="Crigler-Najjar syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79237" />
        <display value="Galactokinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79238" />
        <display value="Galactose epimerase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79239" />
        <display value="Classic galactosemia" />
      </concept>
      <concept>
        <code value="ORPHA:79240" />
        <display value="Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79241" />
        <display value="Biotinidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79242" />
        <display value="Holocarboxylase synthetase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79243" />
        <display value="Pyruvate dehydrogenase E1-alpha deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79244" />
        <display value="Pyruvate dehydrogenase E2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79246" />
        <display value="Pyruvate dehydrogenase phosphatase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79253" />
        <display value="Mild phenylketonuria" />
      </concept>
      <concept>
        <code value="ORPHA:79254" />
        <display value="Classic phenylketonuria" />
      </concept>
      <concept>
        <code value="ORPHA:79255" />
        <display value="GM1 gangliosidosis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:79256" />
        <display value="GM1 gangliosidosis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79257" />
        <display value="GM1 gangliosidosis type 3" />
      </concept>
      <concept>
        <code value="ORPHA:79258" />
        <display value="Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia" />
      </concept>
      <concept>
        <code value="ORPHA:79259" />
        <display value="Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib" />
      </concept>
      <concept>
        <code value="ORPHA:79262" />
        <display value="Adult neuronal ceroid lipofuscinosis" />
      </concept>
      <concept>
        <code value="ORPHA:79263" />
        <display value="Infantile neuronal ceroid lipofuscinosis" />
      </concept>
      <concept>
        <code value="ORPHA:79264" />
        <display value="Juvenile neuronal ceroid lipofuscinosis" />
      </concept>
      <concept>
        <code value="ORPHA:79269" />
        <display value="Sanfilippo syndrome type A" />
      </concept>
      <concept>
        <code value="ORPHA:79270" />
        <display value="Sanfilippo syndrome type B" />
      </concept>
      <concept>
        <code value="ORPHA:79271" />
        <display value="Sanfilippo syndrome type C" />
      </concept>
      <concept>
        <code value="ORPHA:79272" />
        <display value="Sanfilippo syndrome type D" />
      </concept>
      <concept>
        <code value="ORPHA:79273" />
        <display value="Hereditary coproporphyria" />
      </concept>
      <concept>
        <code value="ORPHA:79276" />
        <display value="Acute intermittent porphyria" />
      </concept>
      <concept>
        <code value="ORPHA:79277" />
        <display value="Congenital erythropoietic porphyria" />
      </concept>
      <concept>
        <code value="ORPHA:79278" />
        <display value="Autosomal erythropoietic protoporphyria" />
      </concept>
      <concept>
        <code value="ORPHA:79279" />
        <display value="Alpha-N-acetylgalactosaminidase deficiency type 1" />
      </concept>
      <concept>
        <code value="ORPHA:79280" />
        <display value="Alpha-N-acetylgalactosaminidase deficiency type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79281" />
        <display value="Alpha-N-acetylgalactosaminidase deficiency type 3" />
      </concept>
      <concept>
        <code value="ORPHA:79282" />
        <display value="Methylmalonic acidemia with homocystinuria, type cblC" />
      </concept>
      <concept>
        <code value="ORPHA:79283" />
        <display value="Methylmalonic acidemia with homocystinuria, type cblD" />
      </concept>
      <concept>
        <code value="ORPHA:79284" />
        <display value="Methylmalonic acidemia with homocystinuria type cblF" />
      </concept>
      <concept>
        <code value="ORPHA:79292" />
        <display value="Fish-eye disease" />
      </concept>
      <concept>
        <code value="ORPHA:79293" />
        <display value="Familial LCAT deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79298" />
        <display value="Diazoxide-resistant focal hyperinsulinism" />
      </concept>
      <concept>
        <code value="ORPHA:79299" />
        <display value="Hyperinsulinism due to glucokinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:793" />
        <display value="SAPHO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79301" />
        <display value="Congenital bile acid synthesis defect type 1" />
      </concept>
      <concept>
        <code value="ORPHA:79302" />
        <display value="Congenital bile acid synthesis defect type 3" />
      </concept>
      <concept>
        <code value="ORPHA:79303" />
        <display value="Congenital bile acid synthesis defect type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79304" />
        <display value="Progressive familial intrahepatic cholestasis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79305" />
        <display value="Progressive familial intrahepatic cholestasis type 3" />
      </concept>
      <concept>
        <code value="ORPHA:79306" />
        <display value="Progressive familial intrahepatic cholestasis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:79310" />
        <display value="Vitamin B12-responsive methylmalonic acidemia type cblA" />
      </concept>
      <concept>
        <code value="ORPHA:79311" />
        <display value="Vitamin B12-responsive methylmalonic acidemia type cblB" />
      </concept>
      <concept>
        <code value="ORPHA:79312" />
        <display value="Vitamin B12-unresponsive methylmalonic acidemia type mut-" />
      </concept>
      <concept>
        <code value="ORPHA:79314" />
        <display value="L-2-hydroxyglutaric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:79315" />
        <display value="D-2-hydroxyglutaric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:79318" />
        <display value="PMM2-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79319" />
        <display value="MPI-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79320" />
        <display value="ALG6-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79321" />
        <display value="ALG3-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79322" />
        <display value="DPM1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79323" />
        <display value="MPDU1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79324" />
        <display value="ALG12-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79325" />
        <display value="ALG8-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79326" />
        <display value="ALG2-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79327" />
        <display value="ALG1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79328" />
        <display value="ALG9-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79329" />
        <display value="MGAT2-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79330" />
        <display value="MOGS-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79332" />
        <display value="B4GALT1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79333" />
        <display value="COG7-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:79344" />
        <display value="Autosomal dominant chondrodysplasia punctata" />
      </concept>
      <concept>
        <code value="ORPHA:79345" />
        <display value="Brachytelephalangic chondrodysplasia punctata" />
      </concept>
      <concept>
        <code value="ORPHA:79346" />
        <display value="Chondrodysplasia punctata, tibial-metacarpal type" />
      </concept>
      <concept>
        <code value="ORPHA:79347" />
        <display value="Chondrodysplasia punctata, Toriello type" />
      </concept>
      <concept>
        <code value="ORPHA:79350" />
        <display value="3-phosphoserine phosphatase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79351" />
        <display value="3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form" />
      </concept>
      <concept>
        <code value="ORPHA:79353" />
        <display value="Epidermal disease" />
      </concept>
      <concept>
        <code value="ORPHA:79354" />
        <display value="Ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:79355" />
        <display value="Erythrokeratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:79356" />
        <display value="Acrokeratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:79357" />
        <display value="Hereditary palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:79358" />
        <display value="Porokeratosis" />
      </concept>
      <concept>
        <code value="ORPHA:79359" />
        <display value="Other epidermal disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79360" />
        <display value="Other genetic epidermal disease" />
      </concept>
      <concept>
        <code value="ORPHA:79361" />
        <display value="Inherited epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:79362" />
        <display value="Epidermal appendage anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:79363" />
        <display value="Hair anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:79364" />
        <display value="Alopecia" />
      </concept>
      <concept>
        <code value="ORPHA:79365" />
        <display value="Rare disorder with hypertrichosis" />
      </concept>
      <concept>
        <code value="ORPHA:79366" />
        <display value="Isolated hair shaft abnormality" />
      </concept>
      <concept>
        <code value="ORPHA:79367" />
        <display value="Syndromic hair shaft abnormality" />
      </concept>
      <concept>
        <code value="ORPHA:79368" />
        <display value="Nail anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:79369" />
        <display value="Isolated nail anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:79370" />
        <display value="Syndromic nail anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:79372" />
        <display value="Sebaceous gland anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:79373" />
        <display value="Ectodermal dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79374" />
        <display value="Pigmentation anomaly of the skin" />
      </concept>
      <concept>
        <code value="ORPHA:79375" />
        <display value="Hyperpigmentation of the skin" />
      </concept>
      <concept>
        <code value="ORPHA:79376" />
        <display value="Hypopigmentation of the skin" />
      </concept>
      <concept>
        <code value="ORPHA:79377" />
        <display value="Dermis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79378" />
        <display value="Dermis elastic tissue disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79379" />
        <display value="Skin vascular disease" />
      </concept>
      <concept>
        <code value="ORPHA:79380" />
        <display value="Mixed dermis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79381" />
        <display value="Other dermis disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79382" />
        <display value="Subcutaneous tissue disease" />
      </concept>
      <concept>
        <code value="ORPHA:79383" />
        <display value="Lymphedema" />
      </concept>
      <concept>
        <code value="ORPHA:79384" />
        <display value="Rare urticaria" />
      </concept>
      <concept>
        <code value="ORPHA:79385" />
        <display value="Unclassified genetic skin disorder" />
      </concept>
      <concept>
        <code value="ORPHA:79386" />
        <display value="Rare skin tumor or hamartoma" />
      </concept>
      <concept>
        <code value="ORPHA:79387" />
        <display value="Metabolic disease with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:79388" />
        <display value="Mucopolysaccharidosis with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:79389" />
        <display value="Premature aging" />
      </concept>
      <concept>
        <code value="ORPHA:79390" />
        <display value="Rare photodermatosis" />
      </concept>
      <concept>
        <code value="ORPHA:79391" />
        <display value="Immune deficiency with skin involvement" />
      </concept>
      <concept>
        <code value="ORPHA:79394" />
        <display value="Congenital non-bullous ichthyosiform erythroderma" />
      </concept>
      <concept>
        <code value="ORPHA:79395" />
        <display value="Keratoderma hereditarium mutilans with ichthyosis" />
      </concept>
      <concept>
        <code value="ORPHA:79396" />
        <display value="Epidermolysis bullosa simplex, generalized severe" />
      </concept>
      <concept>
        <code value="ORPHA:79397" />
        <display value="Epidermolysis bullosa simplex with mottled pigmentation" />
      </concept>
      <concept>
        <code value="ORPHA:79399" />
        <display value="Epidermolysis bullosa simplex, generalized intermediate" />
      </concept>
      <concept>
        <code value="ORPHA:794" />
        <display value="Saethre-Chotzen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79400" />
        <display value="Localized epidermolysis bullosa simplex" />
      </concept>
      <concept>
        <code value="ORPHA:79401" />
        <display value="Epidermolysis bullosa simplex, Ogna type" />
      </concept>
      <concept>
        <code value="ORPHA:79402" />
        <display value="Junctional epidermolysis bullosa, generalized intermediate" />
      </concept>
      <concept>
        <code value="ORPHA:79403" />
        <display value="Junctional epidermolysis bullosa-pyloric atresia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79404" />
        <display value="Junctional epidermolysis bullosa, generalized severe" />
      </concept>
      <concept>
        <code value="ORPHA:79405" />
        <display value="Junctional epidermolysis bullosa inversa" />
      </concept>
      <concept>
        <code value="ORPHA:79406" />
        <display value="Late-onset junctional epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:79408" />
        <display value="Severe generalized recessive dystrophic epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:79409" />
        <display value="Recessive dystrophic epidermolysis bullosa inversa" />
      </concept>
      <concept>
        <code value="ORPHA:79410" />
        <display value="Pretibial dystrophic epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:79411" />
        <display value="Transient bullous dermolysis of the newborn" />
      </concept>
      <concept>
        <code value="ORPHA:79414" />
        <display value="Woolly hair nevus" />
      </concept>
      <concept>
        <code value="ORPHA:79430" />
        <display value="Hermansky-Pudlak syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79431" />
        <display value="Oculocutaneous albinism type 1A" />
      </concept>
      <concept>
        <code value="ORPHA:79432" />
        <display value="Oculocutaneous albinism type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79433" />
        <display value="Oculocutaneous albinism type 3" />
      </concept>
      <concept>
        <code value="ORPHA:79434" />
        <display value="Oculocutaneous albinism type 1B" />
      </concept>
      <concept>
        <code value="ORPHA:79435" />
        <display value="Oculocutaneous albinism type 4" />
      </concept>
      <concept>
        <code value="ORPHA:79443" />
        <display value="Pseudohypoparathyroidism type 1A" />
      </concept>
      <concept>
        <code value="ORPHA:79444" />
        <display value="Pseudohypoparathyroidism type 1C" />
      </concept>
      <concept>
        <code value="ORPHA:79445" />
        <display value="Pseudopseudohypoparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:79447" />
        <display value="X-linked lethal multiple pterygium syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79452" />
        <display value="Milroy disease" />
      </concept>
      <concept>
        <code value="ORPHA:79455" />
        <display value="Cutaneous mastocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:79456" />
        <display value="Diffuse cutaneous mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:79457" />
        <display value="Maculopapular cutaneous mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:79459" />
        <display value="Follicular atrophoderma-basal cell carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:79466" />
        <display value="Inflammatory linear verrucous epidermal nevus" />
      </concept>
      <concept>
        <code value="ORPHA:79467" />
        <display value="Verrucous nevus" />
      </concept>
      <concept>
        <code value="ORPHA:79468" />
        <display value="Acanthokeratolytic verrucous nevus" />
      </concept>
      <concept>
        <code value="ORPHA:79473" />
        <display value="Porphyria variegata" />
      </concept>
      <concept>
        <code value="ORPHA:79474" />
        <display value="Atypical Werner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79476" />
        <display value="Griscelli syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:79477" />
        <display value="Griscelli syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79478" />
        <display value="Griscelli syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:79479" />
        <display value="Pemphigus vegetans" />
      </concept>
      <concept>
        <code value="ORPHA:79480" />
        <display value="Pemphigus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:79481" />
        <display value="Pemphigus foliaceus" />
      </concept>
      <concept>
        <code value="ORPHA:79483" />
        <display value="Phakomatosis cesioflammea" />
      </concept>
      <concept>
        <code value="ORPHA:79484" />
        <display value="Phakomatosis cesiomarmorata" />
      </concept>
      <concept>
        <code value="ORPHA:79485" />
        <display value="Phakomatosis spilorosea" />
      </concept>
      <concept>
        <code value="ORPHA:79486" />
        <display value="Cystic hygroma" />
      </concept>
      <concept>
        <code value="ORPHA:79489" />
        <display value="Macrocystic lymphatic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:79490" />
        <display value="Microcystic lymphatic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:79492" />
        <display value="Pili gemini" />
      </concept>
      <concept>
        <code value="ORPHA:79493" />
        <display value="Brooke-Spiegler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79495" />
        <display value="X-linked congenital generalized hypertrichosis" />
      </concept>
      <concept>
        <code value="ORPHA:79499" />
        <display value="Autosomal dominant deafness-onychodystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:795" />
        <display value="Rare form of salmonellosis" />
      </concept>
      <concept>
        <code value="ORPHA:79500" />
        <display value="DOORS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79501" />
        <display value="Punctate palmoplantar keratoderma type 1" />
      </concept>
      <concept>
        <code value="ORPHA:79502" />
        <display value="Punctate palmoplantar keratoderma type 2" />
      </concept>
      <concept>
        <code value="ORPHA:79503" />
        <display value="Ichthyosis hystrix of Curth-Macklin" />
      </concept>
      <concept>
        <code value="ORPHA:79506" />
        <display value="Cholesterol-ester transfer protein deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79507" />
        <display value="Hypotonia-failure to thrive-microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:796" />
        <display value="Sandhoff disease" />
      </concept>
      <concept>
        <code value="ORPHA:79643" />
        <display value="Autosomal recessive hyperinsulinism due to SUR1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79644" />
        <display value="Autosomal recessive hyperinsulinism due to Kir6.2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:79651" />
        <display value="Mild hyperphenylalaninemia" />
      </concept>
      <concept>
        <code value="ORPHA:79665" />
        <display value="Gardner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:79669" />
        <display value="Autoimmune bullous skin disease" />
      </concept>
      <concept>
        <code value="ORPHA:797" />
        <display value="Sarcoidosis" />
      </concept>
      <concept>
        <code value="ORPHA:798" />
        <display value="Schinzel-Giedion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:799" />
        <display value="Schizencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:8" />
        <display value="47,XYY syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:800" />
        <display value="Schwartz-Jampel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:801" />
        <display value="Scleroderma" />
      </concept>
      <concept>
        <code value="ORPHA:803" />
        <display value="Amyotrophic lateral sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:805" />
        <display value="Tuberous sclerosis complex" />
      </concept>
      <concept>
        <code value="ORPHA:806" />
        <display value="Scott syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:808" />
        <display value="Seckel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:809" />
        <display value="Mixed connective tissue disease" />
      </concept>
      <concept>
        <code value="ORPHA:81" />
        <display value="Antisynthetase syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:810" />
        <display value="Shigellosis" />
      </concept>
      <concept>
        <code value="ORPHA:811" />
        <display value="Shwachman-Diamond syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:812" />
        <display value="Sialidosis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:813" />
        <display value="Silver-Russell syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:816" />
        <display value="Sjogren-Larsson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:817" />
        <display value="Peeling skin syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:818" />
        <display value="Smith-Lemli-Opitz syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:819" />
        <display value="Smith-Magenis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:82" />
        <display value="Hereditary thrombophilia due to congenital antithrombin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:820" />
        <display value="Sneddon syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:82004" />
        <display value="Ehlers-Danlos syndrome with periventricular heterotopia" />
      </concept>
      <concept>
        <code value="ORPHA:821" />
        <display value="Sotos syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:822" />
        <display value="Hereditary spherocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:823" />
        <display value="Isolated spina bifida" />
      </concept>
      <concept>
        <code value="ORPHA:824" />
        <display value="Primary myelofibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:826" />
        <display value="Sporotrichosis" />
      </concept>
      <concept>
        <code value="ORPHA:827" />
        <display value="Stargardt disease" />
      </concept>
      <concept>
        <code value="ORPHA:828" />
        <display value="Stickler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:829" />
        <display value="Adult-onset Still disease" />
      </concept>
      <concept>
        <code value="ORPHA:83" />
        <display value="Antley-Bixler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83001" />
        <display value="Urogenital tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:831" />
        <display value="Congenital cervical spinal stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:832" />
        <display value="Succinyl-CoA:3-ketoacid CoA transferase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:833" />
        <display value="Encephalopathy due to sulfite oxidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:83311" />
        <display value="Rocky Mountain spotted fever" />
      </concept>
      <concept>
        <code value="ORPHA:83312" />
        <display value="Rickettsialpox" />
      </concept>
      <concept>
        <code value="ORPHA:83313" />
        <display value="Boutonneuse fever" />
      </concept>
      <concept>
        <code value="ORPHA:83314" />
        <display value="Epidemic typhus" />
      </concept>
      <concept>
        <code value="ORPHA:83315" />
        <display value="Murine typhus" />
      </concept>
      <concept>
        <code value="ORPHA:83316" />
        <display value="Pseudotyphus of California" />
      </concept>
      <concept>
        <code value="ORPHA:83317" />
        <display value="Scrub typhus" />
      </concept>
      <concept>
        <code value="ORPHA:83330" />
        <display value="Proximal spinal muscular atrophy type 1" />
      </concept>
      <concept>
        <code value="ORPHA:834" />
        <display value="Free sialic acid storage disease" />
      </concept>
      <concept>
        <code value="ORPHA:83418" />
        <display value="Proximal spinal muscular atrophy type 2" />
      </concept>
      <concept>
        <code value="ORPHA:83419" />
        <display value="Proximal spinal muscular atrophy type 3" />
      </concept>
      <concept>
        <code value="ORPHA:83420" />
        <display value="Proximal spinal muscular atrophy type 4" />
      </concept>
      <concept>
        <code value="ORPHA:83450" />
        <display value="Regional odontodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:83451" />
        <display value="Florid cemento-osseous dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:83452" />
        <display value="Complex regional pain syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83453" />
        <display value="Vulvovaginal gingival syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83454" />
        <display value="Glomuvenous malformation" />
      </concept>
      <concept>
        <code value="ORPHA:83461" />
        <display value="Congenital primary aphakia" />
      </concept>
      <concept>
        <code value="ORPHA:83463" />
        <display value="Microtia" />
      </concept>
      <concept>
        <code value="ORPHA:83465" />
        <display value="Narcolepsy type 2" />
      </concept>
      <concept>
        <code value="ORPHA:83467" />
        <display value="Morvan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83468" />
        <display value="Solitary bone cyst" />
      </concept>
      <concept>
        <code value="ORPHA:83469" />
        <display value="Desmoplastic small round cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:83471" />
        <display value="Thymic aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:83472" />
        <display value="CAMOS syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83473" />
        <display value="Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83476" />
        <display value="West-Nile encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:83482" />
        <display value="Mycoplasma encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:83483" />
        <display value="La Crosse encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:83484" />
        <display value="St. Louis encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:83593" />
        <display value="Western equine encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:83594" />
        <display value="Eastern equine encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:83595" />
        <display value="Colorado tick fever" />
      </concept>
      <concept>
        <code value="ORPHA:83597" />
        <display value="Acute disseminated encephalomyelitis" />
      </concept>
      <concept>
        <code value="ORPHA:83600" />
        <display value="Encephalitis lethargica" />
      </concept>
      <concept>
        <code value="ORPHA:83601" />
        <display value="Steroid-responsive encephalopathy associated with autoimmune thyroiditis" />
      </concept>
      <concept>
        <code value="ORPHA:83616" />
        <display value="Rubella panencephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:83617" />
        <display value="Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83619" />
        <display value="Macrostomia-preauricular tags-external ophthalmoplegia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83620" />
        <display value="Enteric anendocrinosis" />
      </concept>
      <concept>
        <code value="ORPHA:83628" />
        <display value="LUMBAR syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83629" />
        <display value="Leukoencephalopathy-metaphyseal chondrodysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:83639" />
        <display value="Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:83642" />
        <display value="Microcytic anemia with liver iron overload" />
      </concept>
      <concept>
        <code value="ORPHA:83648" />
        <display value="X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:838" />
        <display value="Susac syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:839" />
        <display value="Congenital nephrotic syndrome, Finnish type" />
      </concept>
      <concept>
        <code value="ORPHA:84" />
        <display value="Fanconi anemia" />
      </concept>
      <concept>
        <code value="ORPHA:840" />
        <display value="Syringocystadenoma papilliferum" />
      </concept>
      <concept>
        <code value="ORPHA:84064" />
        <display value="Syndromic diarrhea" />
      </concept>
      <concept>
        <code value="ORPHA:84065" />
        <display value="Idiopathic malabsorption due to bile acid synthesis defects" />
      </concept>
      <concept>
        <code value="ORPHA:84081" />
        <display value="Senior-Boichis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:84085" />
        <display value="Hinman syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:84087" />
        <display value="Collagen type III glomerulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:84090" />
        <display value="Fibronectin glomerulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:84093" />
        <display value="Hereditary thermosensitive neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:841" />
        <display value="Sebocystomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:84132" />
        <display value="Desmin-related myopathy with Mallory body-like inclusions" />
      </concept>
      <concept>
        <code value="ORPHA:84142" />
        <display value="Isaac syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:842" />
        <display value="Testicular seminomatous germ cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:84271" />
        <display value="Sporadic idiopathic steroid-resistant nephrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:844" />
        <display value="Lown-Ganong-Levine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:845" />
        <display value="Tay-Sachs disease" />
      </concept>
      <concept>
        <code value="ORPHA:846" />
        <display value="Alpha-thalassemia" />
      </concept>
      <concept>
        <code value="ORPHA:847" />
        <display value="Alpha-thalassemia-X-linked intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:848" />
        <display value="Beta-thalassemia" />
      </concept>
      <concept>
        <code value="ORPHA:849" />
        <display value="Glanzmann thrombasthenia" />
      </concept>
      <concept>
        <code value="ORPHA:85" />
        <display value="Congenital dyserythropoietic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:851" />
        <display value="Paris-Trousseau thrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:85102" />
        <display value="Perineurioma" />
      </concept>
      <concept>
        <code value="ORPHA:85110" />
        <display value="Familial encephalopathy with neuroserpin inclusion bodies" />
      </concept>
      <concept>
        <code value="ORPHA:85112" />
        <display value="Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85128" />
        <display value="Bothnia retinal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:85136" />
        <display value="Cystic leukoencephalopathy without megalencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:85138" />
        <display value="Addison disease" />
      </concept>
      <concept>
        <code value="ORPHA:85146" />
        <display value="Neurogenic scapuloperoneal syndrome, Kaeser type" />
      </concept>
      <concept>
        <code value="ORPHA:85162" />
        <display value="Facial onset sensory and motor neuronopathy" />
      </concept>
      <concept>
        <code value="ORPHA:85163" />
        <display value="Hypomyelination-congenital cataract syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85164" />
        <display value="Camptodactyly-tall stature-scoliosis-hearing loss syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85165" />
        <display value="Severe achondroplasia-developmental delay-acanthosis nigricans syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85166" />
        <display value="Platyspondylic dysplasia, Torrance type" />
      </concept>
      <concept>
        <code value="ORPHA:85167" />
        <display value="Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85168" />
        <display value="Craniofacial conodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:85169" />
        <display value="Familial digital arthropathy-brachydactyly" />
      </concept>
      <concept>
        <code value="ORPHA:85170" />
        <display value="Mesomelic dysplasia, Savarirayan type" />
      </concept>
      <concept>
        <code value="ORPHA:85172" />
        <display value="Microcephalic osteodysplastic dysplasia, Saul-Wilson type" />
      </concept>
      <concept>
        <code value="ORPHA:85173" />
        <display value="IMAGe syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85174" />
        <display value="Pseudodiastrophic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:85175" />
        <display value="Astley-Kendall dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:85179" />
        <display value="Infantile osteopetrosis with neuroaxonal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:85182" />
        <display value="Diaphyseal medullary stenosis-bone malignancy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85184" />
        <display value="Craniometadiaphyseal dysplasia, wormian bone type" />
      </concept>
      <concept>
        <code value="ORPHA:85186" />
        <display value="Endosteal sclerosis-cerebellar hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85188" />
        <display value="Metaphyseal dysplasia, Braun-Tinschert type" />
      </concept>
      <concept>
        <code value="ORPHA:85191" />
        <display value="Singleton-Merten dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:85192" />
        <display value="Calvarial doughnut lesions-bone fragility syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85193" />
        <display value="Idiopathic juvenile osteoporosis" />
      </concept>
      <concept>
        <code value="ORPHA:85194" />
        <display value="Spondylo-ocular syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85195" />
        <display value="Familial expansile osteolysis" />
      </concept>
      <concept>
        <code value="ORPHA:85196" />
        <display value="Nodulosis-arthropathy-osteolysis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85197" />
        <display value="Genochondromatosis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:85198" />
        <display value="Dysspondyloenchondromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:85199" />
        <display value="Craniosynostosis-anal anomalies-porokeratosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:852" />
        <display value="X-linked thrombocytopenia with normal platelets" />
      </concept>
      <concept>
        <code value="ORPHA:85200" />
        <display value="Ischio-vertebral syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85201" />
        <display value="Genitopatellar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85202" />
        <display value="Keutel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85203" />
        <display value="Acropectoral syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85212" />
        <display value="Fetal Gaucher disease" />
      </concept>
      <concept>
        <code value="ORPHA:85273" />
        <display value="X-linked intellectual disability, Abidi type" />
      </concept>
      <concept>
        <code value="ORPHA:85274" />
        <display value="Syndromic X-linked intellectual disability 7" />
      </concept>
      <concept>
        <code value="ORPHA:85275" />
        <display value="Microphthalmia-ankyloblepharon-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85276" />
        <display value="X-linked intellectual disability, Armfield type" />
      </concept>
      <concept>
        <code value="ORPHA:85277" />
        <display value="X-linked intellectual disability, Cantagrel type" />
      </concept>
      <concept>
        <code value="ORPHA:85278" />
        <display value="Christianson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85279" />
        <display value="Syndromic X-linked intellectual disability due to JARID1C mutation" />
      </concept>
      <concept>
        <code value="ORPHA:85280" />
        <display value="X-linked intellectual disability-cubitus valgus-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85282" />
        <display value="MEHMO syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85283" />
        <display value="X-linked intellectual disability, Miles-Carpenter type" />
      </concept>
      <concept>
        <code value="ORPHA:85284" />
        <display value="BRESEK syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85285" />
        <display value="X-linked intellectual disability, Schimke type" />
      </concept>
      <concept>
        <code value="ORPHA:85286" />
        <display value="X-linked intellectual disability, Shashi type" />
      </concept>
      <concept>
        <code value="ORPHA:85287" />
        <display value="X-linked intellectual disability, Siderius type" />
      </concept>
      <concept>
        <code value="ORPHA:85288" />
        <display value="X-linked intellectual disability, Stocco Dos Santos type" />
      </concept>
      <concept>
        <code value="ORPHA:85290" />
        <display value="X-linked intellectual disability, Wilson type" />
      </concept>
      <concept>
        <code value="ORPHA:85292" />
        <display value="X-linked spinocerebellar ataxia type 4" />
      </concept>
      <concept>
        <code value="ORPHA:85293" />
        <display value="X-linked intellectual disability, Cabezas type" />
      </concept>
      <concept>
        <code value="ORPHA:85294" />
        <display value="X-linked epilepsy-learning disabilities-behavior disorders syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85295" />
        <display value="HSD10 disease, atypical type" />
      </concept>
      <concept>
        <code value="ORPHA:85297" />
        <display value="X-linked spinocerebellar ataxia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:853" />
        <display value="Fetal and neonatal alloimmune thrombocytopenia" />
      </concept>
      <concept>
        <code value="ORPHA:85317" />
        <display value="X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85319" />
        <display value="X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85320" />
        <display value="X-linked intellectual disability-macrocephaly-macroorchidism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85321" />
        <display value="Deafness-intellectual disability syndrome, Martin-Probst type" />
      </concept>
      <concept>
        <code value="ORPHA:85322" />
        <display value="X-linked intellectual disability, Pai type" />
      </concept>
      <concept>
        <code value="ORPHA:85323" />
        <display value="X-linked intellectual disability, Seemanova type" />
      </concept>
      <concept>
        <code value="ORPHA:85324" />
        <display value="X-linked intellectual disability, Shrimpton type" />
      </concept>
      <concept>
        <code value="ORPHA:85325" />
        <display value="X-linked intellectual disability, Stevenson type" />
      </concept>
      <concept>
        <code value="ORPHA:85326" />
        <display value="X-linked intellectual disability, Stoll type" />
      </concept>
      <concept>
        <code value="ORPHA:85327" />
        <display value="X-linked intellectual disability-acromegaly-hyperactivity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85328" />
        <display value="X-linked intellectual disability, Turner type" />
      </concept>
      <concept>
        <code value="ORPHA:85329" />
        <display value="X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85330" />
        <display value="X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85332" />
        <display value="X-linked intellectual disability-retinitis pigmentosa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85334" />
        <display value="X-linked neurodegenerative syndrome, Bertini type" />
      </concept>
      <concept>
        <code value="ORPHA:85335" />
        <display value="Fried syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85336" />
        <display value="X-linked neurodegenerative syndrome, Hamel type" />
      </concept>
      <concept>
        <code value="ORPHA:85338" />
        <display value="X-linked intellectual disability-ataxia-apraxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:854" />
        <display value="Primitive portal vein thrombosis" />
      </concept>
      <concept>
        <code value="ORPHA:85408" />
        <display value="Rheumatoid factor-negative juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:85410" />
        <display value="Oligoarticular juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:85414" />
        <display value="Systemic-onset juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:85435" />
        <display value="Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:85436" />
        <display value="Psoriasis-related juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:85438" />
        <display value="Enthesitis-related juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:85442" />
        <display value="Short stature-pituitary and cerebellar defects-small sella turcica syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:85443" />
        <display value="AL amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:85445" />
        <display value="AA amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:85446" />
        <display value="Wild type ABeta2M amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:85447" />
        <display value="ATTRV30M amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:85448" />
        <display value="AGel amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:85450" />
        <display value="Hereditary amyloidosis with primary renal involement" />
      </concept>
      <concept>
        <code value="ORPHA:85451" />
        <display value="ATTRV122I amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:85453" />
        <display value="X-linked reticulate pigmentary disorder" />
      </concept>
      <concept>
        <code value="ORPHA:85458" />
        <display value="Hereditary cerebral hemorrhage with amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:857" />
        <display value="Townes-Brocks syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:858" />
        <display value="Congenital toxoplasmosis" />
      </concept>
      <concept>
        <code value="ORPHA:859" />
        <display value="Transcobalamin deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:86" />
        <display value="Familial abdominal aortic aneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:860" />
        <display value="Congenitally uncorrected transposition of the great arteries" />
      </concept>
      <concept>
        <code value="ORPHA:861" />
        <display value="Treacher-Collins syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:863" />
        <display value="Trichinellosis" />
      </concept>
      <concept>
        <code value="ORPHA:86309" />
        <display value="DPAGT1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:864" />
        <display value="Trichofolliculoma" />
      </concept>
      <concept>
        <code value="ORPHA:867" />
        <display value="Familial multiple trichoepithelioma" />
      </concept>
      <concept>
        <code value="ORPHA:86788" />
        <display value="X-linked severe congenital neutropenia" />
      </concept>
      <concept>
        <code value="ORPHA:86789" />
        <display value="Patella aplasia/hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:86795" />
        <display value="Localized lichen myxedematosus" />
      </concept>
      <concept>
        <code value="ORPHA:86797" />
        <display value="Atypical lichen myxedematosus" />
      </concept>
      <concept>
        <code value="ORPHA:868" />
        <display value="Triose phosphate-isomerase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:86812" />
        <display value="Autosomal recessive limb-girdle muscular dystrophy type 2K" />
      </concept>
      <concept>
        <code value="ORPHA:86813" />
        <display value="Helicoid peripapillary chorioretinal degeneration" />
      </concept>
      <concept>
        <code value="ORPHA:86814" />
        <display value="Benign adult familial myoclonic epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:86815" />
        <display value="Aplasia of lacrimal and salivary glands" />
      </concept>
      <concept>
        <code value="ORPHA:86816" />
        <display value="Congenital analbuminemia" />
      </concept>
      <concept>
        <code value="ORPHA:86817" />
        <display value="Hemolytic anemia due to adenylate kinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:86818" />
        <display value="Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86819" />
        <display value="Atrichia with papular lesions" />
      </concept>
      <concept>
        <code value="ORPHA:86820" />
        <display value="Familial avascular necrosis of femoral head" />
      </concept>
      <concept>
        <code value="ORPHA:86821" />
        <display value="Lissencephaly type 3-familial fetal akinesia sequence syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86822" />
        <display value="Lissencephaly type 3-metacarpal bone dysplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86823" />
        <display value="Lissencephaly with cerebellar hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:86829" />
        <display value="Chronic neutrophilic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:86830" />
        <display value="Chronic myeloproliferative disease, unclassifiable" />
      </concept>
      <concept>
        <code value="ORPHA:86834" />
        <display value="Juvenile myelomonocytic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:86836" />
        <display value="Refractory cytopenia with multilineage dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:86839" />
        <display value="Refractory anemia with excess blasts" />
      </concept>
      <concept>
        <code value="ORPHA:86841" />
        <display value="Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality" />
      </concept>
      <concept>
        <code value="ORPHA:86843" />
        <display value="Acute panmyelosis with myelofibrosis" />
      </concept>
      <concept>
        <code value="ORPHA:86845" />
        <display value="Acute myeloid leukaemia with myelodysplasia-related features" />
      </concept>
      <concept>
        <code value="ORPHA:86846" />
        <display value="Therapy related acute myeloid leukemia and myelodysplastic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86849" />
        <display value="Acute basophilic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:86850" />
        <display value="Myeloid sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:86851" />
        <display value="Acute leukemia of ambiguous lineage" />
      </concept>
      <concept>
        <code value="ORPHA:86852" />
        <display value="B-cell prolymphocytic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:86854" />
        <display value="Splenic marginal zone lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86855" />
        <display value="Plasmacytoma" />
      </concept>
      <concept>
        <code value="ORPHA:86861" />
        <display value="Non-amyloid monoclonal immunoglobulin deposition disease" />
      </concept>
      <concept>
        <code value="ORPHA:86864" />
        <display value="Heavy chain disease" />
      </concept>
      <concept>
        <code value="ORPHA:86867" />
        <display value="Nodal marginal zone B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86869" />
        <display value="Lymphomatoid granulomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:86870" />
        <display value="CD4+/CD56+ hematodermic neoplasm" />
      </concept>
      <concept>
        <code value="ORPHA:86871" />
        <display value="T-cell prolymphocytic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:86872" />
        <display value="T-cell large granular lymphocyte leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:86873" />
        <display value="Aggressive NK-cell leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:86875" />
        <display value="Adult T-cell leukemia/lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86879" />
        <display value="Extranodal nasal NK/T cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86880" />
        <display value="Enteropathy-associated T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86882" />
        <display value="Hepatosplenic T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86884" />
        <display value="Subcutaneous panniculitis-like T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86885" />
        <display value="Primary cutaneous peripheral T-cell lymphoma not otherwise specified" />
      </concept>
      <concept>
        <code value="ORPHA:86886" />
        <display value="Angioimmunoblastic T-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86893" />
        <display value="Nodular lymphocyte predominant Hodgkin lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:86896" />
        <display value="Histiocytic sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:86897" />
        <display value="Langerhans cell sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:869" />
        <display value="Triple A syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86900" />
        <display value="Interdigitating dendritic cell sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:86902" />
        <display value="Follicular dendritic cell sarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:86903" />
        <display value="Dendritic cell sarcoma not otherwise specified" />
      </concept>
      <concept>
        <code value="ORPHA:86904" />
        <display value="Methotrexate-associated lymphoproliferative disorders" />
      </concept>
      <concept>
        <code value="ORPHA:86906" />
        <display value="Hypothalamic hamartomas with gelastic seizures" />
      </concept>
      <concept>
        <code value="ORPHA:86908" />
        <display value="Idiopathic hemiconvulsion-hemiplegia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86909" />
        <display value="Myoclonic epilepsy of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:86911" />
        <display value="Epilepsy with myoclonic absences" />
      </concept>
      <concept>
        <code value="ORPHA:86913" />
        <display value="Myoclonic epilepsy in non-progressive encephalopathies" />
      </concept>
      <concept>
        <code value="ORPHA:86914" />
        <display value="Lymphedema-cerebral arteriovenous anomaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86915" />
        <display value="Lymphedema-atrial septal defects-facial changes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86918" />
        <display value="Diffuse palmoplantar keratoderma-acrocyanosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86919" />
        <display value="Keratosis palmaris et plantaris-clinodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:86920" />
        <display value="Dermatopathia pigmentosa reticularis" />
      </concept>
      <concept>
        <code value="ORPHA:86923" />
        <display value="Hereditary palmoplantar keratoderma, Gamborg-Nielsen type" />
      </concept>
      <concept>
        <code value="ORPHA:87" />
        <display value="Apert syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:870" />
        <display value="Down syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:871" />
        <display value="Familial progressive cardiac conduction defect" />
      </concept>
      <concept>
        <code value="ORPHA:87277" />
        <display value="Rare intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:873" />
        <display value="Desmoid tumor" />
      </concept>
      <concept>
        <code value="ORPHA:874" />
        <display value="Primary adult heart tumor" />
      </concept>
      <concept>
        <code value="ORPHA:875" />
        <display value="Primary pediatric heart tumor" />
      </concept>
      <concept>
        <code value="ORPHA:87503" />
        <display value="Mal de Meleda" />
      </concept>
      <concept>
        <code value="ORPHA:876" />
        <display value="Yolk sac tumor" />
      </concept>
      <concept>
        <code value="ORPHA:877" />
        <display value="Neuroendocrine neoplasm" />
      </concept>
      <concept>
        <code value="ORPHA:87876" />
        <display value="Sialidosis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:87884" />
        <display value="Non-syndromic genetic deafness" />
      </concept>
      <concept>
        <code value="ORPHA:879" />
        <display value="Tungiasis" />
      </concept>
      <concept>
        <code value="ORPHA:88" />
        <display value="Idiopathic aplastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:881" />
        <display value="Turner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:882" />
        <display value="Tyrosinemia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:883" />
        <display value="Extragonadal teratoma" />
      </concept>
      <concept>
        <code value="ORPHA:884" />
        <display value="Tetrasomy 12p" />
      </concept>
      <concept>
        <code value="ORPHA:886" />
        <display value="Usher syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88616" />
        <display value="Autosomal recessive non-syndromic intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:88618" />
        <display value="Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:88619" />
        <display value="Familial acute necrotizing encephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:88620" />
        <display value="Isolated congenital anosmia" />
      </concept>
      <concept>
        <code value="ORPHA:88621" />
        <display value="Ichthyosis-prematurity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88628" />
        <display value="Posterior column ataxia-retinitis pigmentosa syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88629" />
        <display value="Tritanopia" />
      </concept>
      <concept>
        <code value="ORPHA:88630" />
        <display value="Terminal osseous dysplasia-pigmentary defects syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88632" />
        <display value="Anterior segment developmental anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:88633" />
        <display value="Superior limbic keratoconjunctivitis" />
      </concept>
      <concept>
        <code value="ORPHA:88635" />
        <display value="Myopathy due to calsequestrin and SERCA1 protein overload" />
      </concept>
      <concept>
        <code value="ORPHA:88637" />
        <display value="Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88639" />
        <display value="Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:88642" />
        <display value="Channelopathy-associated congenital insensitivity to pain" />
      </concept>
      <concept>
        <code value="ORPHA:88643" />
        <display value="Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88644" />
        <display value="Autosomal recessive ataxia, Beauce type" />
      </concept>
      <concept>
        <code value="ORPHA:88659" />
        <display value="Autosomal dominant progressive nephropathy with hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:88660" />
        <display value="Hypertension due to gain-of-function mutations in the mineralocorticoid receptor" />
      </concept>
      <concept>
        <code value="ORPHA:88661" />
        <display value="Amelogenesis imperfecta" />
      </concept>
      <concept>
        <code value="ORPHA:88673" />
        <display value="Hepatocellular carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:887" />
        <display value="VACTERL/VATER association" />
      </concept>
      <concept>
        <code value="ORPHA:888" />
        <display value="Van der Woude syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:889" />
        <display value="Cutaneous leukocytoclastic angiitis" />
      </concept>
      <concept>
        <code value="ORPHA:88917" />
        <display value="X-linked Alport syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88918" />
        <display value="Autosomal dominant Alport syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88919" />
        <display value="Autosomal recessive Alport syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:88924" />
        <display value="Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:88938" />
        <display value="Pseudohypoaldosteronism type 2A" />
      </concept>
      <concept>
        <code value="ORPHA:88939" />
        <display value="Pseudohypoaldosteronism type 2B" />
      </concept>
      <concept>
        <code value="ORPHA:88940" />
        <display value="Pseudohypoaldosteronism type 2C" />
      </concept>
      <concept>
        <code value="ORPHA:88949" />
        <display value="MUC1-related autosomal dominant tubulointerstitial kidney disease" />
      </concept>
      <concept>
        <code value="ORPHA:88950" />
        <display value="UMOD-related autosomal dominant tubulointerstitial kidney disease" />
      </concept>
      <concept>
        <code value="ORPHA:88991" />
        <display value="Rare congenital non-syndromic heart malformation" />
      </concept>
      <concept>
        <code value="ORPHA:88993" />
        <display value="Esophageal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:890" />
        <display value="Hepatic veno-occlusive disease" />
      </concept>
      <concept>
        <code value="ORPHA:89043" />
        <display value="Rare dementia" />
      </concept>
      <concept>
        <code value="ORPHA:891" />
        <display value="Familial exudative vitreoretinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:892" />
        <display value="Von Hippel-Lindau disease" />
      </concept>
      <concept>
        <code value="ORPHA:893" />
        <display value="WAGR syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:894" />
        <display value="Waardenburg syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:895" />
        <display value="Waardenburg syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:896" />
        <display value="Waardenburg syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:897" />
        <display value="Waardenburg-Shah syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:898" />
        <display value="Wagner disease" />
      </concept>
      <concept>
        <code value="ORPHA:89826" />
        <display value="Rare skin disease" />
      </concept>
      <concept>
        <code value="ORPHA:89832" />
        <display value="Syndromic lymphedema" />
      </concept>
      <concept>
        <code value="ORPHA:89838" />
        <display value="Epidermolysis bullosa simplex, autosomal recessive K14" />
      </concept>
      <concept>
        <code value="ORPHA:89839" />
        <display value="Epidermolysis bullosa simplex superficialis" />
      </concept>
      <concept>
        <code value="ORPHA:89840" />
        <display value="Junctional epidermolysis bullosa, non-Herlitz type" />
      </concept>
      <concept>
        <code value="ORPHA:89841" />
        <display value="Centripetalis recessive dystrophic epidermolysis bullosa" />
      </concept>
      <concept>
        <code value="ORPHA:89842" />
        <display value="Recessive dystrophic epidermolysis bullosa, generalized intermediate" />
      </concept>
      <concept>
        <code value="ORPHA:89843" />
        <display value="Dystrophic epidermolysis bullosa pruriginosa" />
      </concept>
      <concept>
        <code value="ORPHA:89844" />
        <display value="Lissencephaly syndrome, Norman-Roberts type" />
      </concept>
      <concept>
        <code value="ORPHA:899" />
        <display value="Walker-Warburg syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:89936" />
        <display value="X-linked hypophosphatemia" />
      </concept>
      <concept>
        <code value="ORPHA:89937" />
        <display value="Autosomal dominant hypophosphatemic rickets" />
      </concept>
      <concept>
        <code value="ORPHA:89938" />
        <display value="Infantile Bartter syndrome with sensorineural deafness" />
      </concept>
      <concept>
        <code value="ORPHA:9" />
        <display value="Tetrasomy X" />
      </concept>
      <concept>
        <code value="ORPHA:90" />
        <display value="Argininemia" />
      </concept>
      <concept>
        <code value="ORPHA:900" />
        <display value="Granulomatosis with polyangiitis" />
      </concept>
      <concept>
        <code value="ORPHA:90000" />
        <display value="Erythema elevatum diutinum" />
      </concept>
      <concept>
        <code value="ORPHA:90001" />
        <display value="X-linked cone dysfunction syndrome with myopia" />
      </concept>
      <concept>
        <code value="ORPHA:90002" />
        <display value="Undifferentiated connective tissue syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90003" />
        <display value="IgG4-related hepatopathy" />
      </concept>
      <concept>
        <code value="ORPHA:90020" />
        <display value="Amyotrophic lateral sclerosis-parkinsonism-dementia complex" />
      </concept>
      <concept>
        <code value="ORPHA:90021" />
        <display value="Radiation myelitis" />
      </concept>
      <concept>
        <code value="ORPHA:90023" />
        <display value="Primary immunodeficiency syndrome due to p14 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90024" />
        <display value="Deafness with labyrinthine aplasia, microtia, and microdontia" />
      </concept>
      <concept>
        <code value="ORPHA:90025" />
        <display value="Non-syndromic syndactyly" />
      </concept>
      <concept>
        <code value="ORPHA:90026" />
        <display value="Primary erythermalgia" />
      </concept>
      <concept>
        <code value="ORPHA:90030" />
        <display value="Hemolytic anemia due to glutathione reductase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90031" />
        <display value="Non-spherocytic hemolytic anemia due to hexokinase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90033" />
        <display value="Autoimmune hemolytic anemia, warm type" />
      </concept>
      <concept>
        <code value="ORPHA:90035" />
        <display value="Paroxysmal cold hemoglobinuria" />
      </concept>
      <concept>
        <code value="ORPHA:90036" />
        <display value="Mixed-type autoimmune hemolytic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:90037" />
        <display value="Drug-induced autoimmune hemolytic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:90038" />
        <display value="Typical hemolytic-uremic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90039" />
        <display value="Hemoglobin D disease" />
      </concept>
      <concept>
        <code value="ORPHA:90041" />
        <display value="Gaisbock syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90042" />
        <display value="Primary familial polycythemia" />
      </concept>
      <concept>
        <code value="ORPHA:90044" />
        <display value="Familial pseudohyperkalemia" />
      </concept>
      <concept>
        <code value="ORPHA:90045" />
        <display value="Hereditary folate malabsorption" />
      </concept>
      <concept>
        <code value="ORPHA:90050" />
        <display value="Retinopathy of prematurity" />
      </concept>
      <concept>
        <code value="ORPHA:90060" />
        <display value="Diffuse alveolar hemorrhage" />
      </concept>
      <concept>
        <code value="ORPHA:90061" />
        <display value="Non-infectious posterior uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:90062" />
        <display value="Acute liver failure" />
      </concept>
      <concept>
        <code value="ORPHA:90065" />
        <display value="Acquired aneurysmal subarachnoid hemorrhage" />
      </concept>
      <concept>
        <code value="ORPHA:90068" />
        <display value="Cocaine intoxication" />
      </concept>
      <concept>
        <code value="ORPHA:90069" />
        <display value="Systemic monochloroacetate poisoning" />
      </concept>
      <concept>
        <code value="ORPHA:90077" />
        <display value="Other acquired skin disease" />
      </concept>
      <concept>
        <code value="ORPHA:901" />
        <display value="Wells syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90103" />
        <display value="Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90114" />
        <display value="Autosomal dominant intermediate Charcot-Marie-Tooth disease" />
      </concept>
      <concept>
        <code value="ORPHA:90117" />
        <display value="Hereditary motor and sensory neuropathy, Okinawa type" />
      </concept>
      <concept>
        <code value="ORPHA:90118" />
        <display value="Severe early-onset axonal neuropathy due to MFN2 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90119" />
        <display value="Hereditary motor and sensory neuropathy with acrodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:90120" />
        <display value="Hereditary motor and sensory neuropathy type 6" />
      </concept>
      <concept>
        <code value="ORPHA:90153" />
        <display value="Mandibuloacral dysplasia with type A lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:90154" />
        <display value="Mandibuloacral dysplasia with type B lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:90156" />
        <display value="Centrifugal lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:90157" />
        <display value="Drug-induced localized lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:90158" />
        <display value="Idiopathic localized lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:90159" />
        <display value="Panniculitis-induced localized lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:90160" />
        <display value="Pressure-induced localized lipoatrophy" />
      </concept>
      <concept>
        <code value="ORPHA:90186" />
        <display value="Meige disease" />
      </concept>
      <concept>
        <code value="ORPHA:902" />
        <display value="Werner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90280" />
        <display value="Chilblain lupus" />
      </concept>
      <concept>
        <code value="ORPHA:90281" />
        <display value="Discoid lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:90282" />
        <display value="Hypertrophic or verrucous lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:90283" />
        <display value="Lupus erythematosus tumidus" />
      </concept>
      <concept>
        <code value="ORPHA:90285" />
        <display value="Lupus erythematosus panniculitis" />
      </concept>
      <concept>
        <code value="ORPHA:90289" />
        <display value="Localized scleroderma" />
      </concept>
      <concept>
        <code value="ORPHA:90290" />
        <display value="CREST syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90291" />
        <display value="Systemic sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:903" />
        <display value="Von Willebrand disease" />
      </concept>
      <concept>
        <code value="ORPHA:90301" />
        <display value="Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90307" />
        <display value="Parkes Weber syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90308" />
        <display value="Klippel-Trenaunay syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90309" />
        <display value="Ehlers-Danlos syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:90318" />
        <display value="Ehlers-Danlos syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:90321" />
        <display value="Cockayne syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:90322" />
        <display value="Cockayne syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:90324" />
        <display value="Cockayne syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:90340" />
        <display value="Blau syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90342" />
        <display value="Xeroderma pigmentosum variant" />
      </concept>
      <concept>
        <code value="ORPHA:90348" />
        <display value="Autosomal dominant cutis laxa" />
      </concept>
      <concept>
        <code value="ORPHA:90349" />
        <display value="Autosomal recessive cutis laxa type 1" />
      </concept>
      <concept>
        <code value="ORPHA:90350" />
        <display value="Autosomal recessive cutis laxa type 2" />
      </concept>
      <concept>
        <code value="ORPHA:90354" />
        <display value="Brittle cornea syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90362" />
        <display value="Primary intestinal lymphangiectasia" />
      </concept>
      <concept>
        <code value="ORPHA:90363" />
        <display value="Secondary intestinal lymphangiectasia" />
      </concept>
      <concept>
        <code value="ORPHA:90368" />
        <display value="Hypotrichosis simplex of the scalp" />
      </concept>
      <concept>
        <code value="ORPHA:90389" />
        <display value="Telangiectasia macularis eruptiva perstans" />
      </concept>
      <concept>
        <code value="ORPHA:90390" />
        <display value="Anonychia-onychodystrophy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90393" />
        <display value="Nodular lichen myxedematosus" />
      </concept>
      <concept>
        <code value="ORPHA:90394" />
        <display value="Discrete papular lichen myxedematosus" />
      </concept>
      <concept>
        <code value="ORPHA:90395" />
        <display value="Papular mucinosis of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:90396" />
        <display value="Acral persistent papular mucinosis" />
      </concept>
      <concept>
        <code value="ORPHA:90397" />
        <display value="Self-healing papular mucinosis" />
      </concept>
      <concept>
        <code value="ORPHA:90398" />
        <display value="Localized lichen myxedematosus with mixed features of different subtypes" />
      </concept>
      <concept>
        <code value="ORPHA:90399" />
        <display value="Localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms" />
      </concept>
      <concept>
        <code value="ORPHA:904" />
        <display value="Williams syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90400" />
        <display value="Scleromyxedema without monoclonal gammopathy" />
      </concept>
      <concept>
        <code value="ORPHA:905" />
        <display value="Wilson disease" />
      </concept>
      <concept>
        <code value="ORPHA:906" />
        <display value="Wiskott-Aldrich syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90625" />
        <display value="X-linked non-syndromic sensorineural deafness type DFN" />
      </concept>
      <concept>
        <code value="ORPHA:90635" />
        <display value="Autosomal dominant non-syndromic sensorineural deafness type DFNA" />
      </concept>
      <concept>
        <code value="ORPHA:90636" />
        <display value="Autosomal recessive non-syndromic sensorineural deafness type DFNB" />
      </concept>
      <concept>
        <code value="ORPHA:90641" />
        <display value="Mitochondrial non-syndromic sensorineural deafness" />
      </concept>
      <concept>
        <code value="ORPHA:90642" />
        <display value="Syndromic genetic deafness" />
      </concept>
      <concept>
        <code value="ORPHA:90646" />
        <display value="Deafness-hypogonadism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90647" />
        <display value="Jervell and Lange-Nielsen syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:90650" />
        <display value="Otopalatodigital syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:90652" />
        <display value="Otopalatodigital syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:90653" />
        <display value="Stickler syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:90654" />
        <display value="Stickler syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:90658" />
        <display value="Charcot-Marie-Tooth disease type 1E" />
      </concept>
      <concept>
        <code value="ORPHA:90673" />
        <display value="Hypothyroidism due to TSH receptor mutations" />
      </concept>
      <concept>
        <code value="ORPHA:90674" />
        <display value="Isolated thyroid-stimulating hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90692" />
        <display value="Rare endocrine growth disease" />
      </concept>
      <concept>
        <code value="ORPHA:90695" />
        <display value="Panhypopituitarism" />
      </concept>
      <concept>
        <code value="ORPHA:90771" />
        <display value="Disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:90776" />
        <display value="46,XX disorder of sex development induced by fetal androgens excess" />
      </concept>
      <concept>
        <code value="ORPHA:90783" />
        <display value="46,XY disorder of sex development due to a testosterone synthesis defect" />
      </concept>
      <concept>
        <code value="ORPHA:90786" />
        <display value="46,XY disorder of sex development due to adrenal and testicular steroidogenesis defect" />
      </concept>
      <concept>
        <code value="ORPHA:90787" />
        <display value="46,XY disorder of sex development due to testicular steroidogenesis defect" />
      </concept>
      <concept>
        <code value="ORPHA:90790" />
        <display value="Congenital lipoid adrenal hyperplasia due to STAR deficency" />
      </concept>
      <concept>
        <code value="ORPHA:90791" />
        <display value="Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90793" />
        <display value="Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90794" />
        <display value="Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90795" />
        <display value="Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90796" />
        <display value="46,XY disorder of sex development due to isolated 17,20-lyase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:90797" />
        <display value="Partial androgen insensitivity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:908" />
        <display value="Fragile X syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:909" />
        <display value="Cerebrotendinous xanthomatosis" />
      </concept>
      <concept>
        <code value="ORPHA:90970" />
        <display value="Primary lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:91" />
        <display value="Aromatase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:910" />
        <display value="Xeroderma pigmentosum" />
      </concept>
      <concept>
        <code value="ORPHA:91024" />
        <display value="Autosomal recessive axonal hereditary motor and sensory neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:91088" />
        <display value="Other metabolic disease" />
      </concept>
      <concept>
        <code value="ORPHA:911" />
        <display value="Combined immunodeficiency due to ZAP70 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:91130" />
        <display value="Cardiomyopathy-hypotonia-lactic acidosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91131" />
        <display value="DK1-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:91132" />
        <display value="Ichthyosis-hypotrichosis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91133" />
        <display value="Osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91135" />
        <display value="Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:91136" />
        <display value="Acquired monoclonal Ig light chain-associated Fanconi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91137" />
        <display value="Immunotactoid or fibrillary glomerulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:91138" />
        <display value="Cryoglobulinemic vasculitis" />
      </concept>
      <concept>
        <code value="ORPHA:91139" />
        <display value="Simple cryoglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:91140" />
        <display value="Unspecified juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:91144" />
        <display value="46,XX disorder of sex development induced by maternal-derived androgen" />
      </concept>
      <concept>
        <code value="ORPHA:912" />
        <display value="Zellweger syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:913" />
        <display value="Zollinger-Ellison syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91347" />
        <display value="TSH-secreting pituitary adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:91348" />
        <display value="Functioning gonadotropic adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:91349" />
        <display value="Non-functioning pituitary adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:91350" />
        <display value="Pituitary deficiency due to Rathkes cleft cysts" />
      </concept>
      <concept>
        <code value="ORPHA:91351" />
        <display value="Pituitary dermoid and epidermoid cysts" />
      </concept>
      <concept>
        <code value="ORPHA:91352" />
        <display value="Germinoma of the central nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:91354" />
        <display value="Pituitary deficiency due to empty sella turcica syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91355" />
        <display value="Sheehan syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91357" />
        <display value="Duplication of the esophagus" />
      </concept>
      <concept>
        <code value="ORPHA:91358" />
        <display value="Congenital esophageal diverticulum" />
      </concept>
      <concept>
        <code value="ORPHA:91359" />
        <display value="Chronic pneumonitis of infancy" />
      </concept>
      <concept>
        <code value="ORPHA:91364" />
        <display value="Non-specific interstitial pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:91378" />
        <display value="Hereditary angioedema" />
      </concept>
      <concept>
        <code value="ORPHA:91385" />
        <display value="Acquired angioedema" />
      </concept>
      <concept>
        <code value="ORPHA:91387" />
        <display value="Familial thoracic aortic aneurysm and aortic dissection" />
      </concept>
      <concept>
        <code value="ORPHA:91396" />
        <display value="Isolated cryptophthalmia" />
      </concept>
      <concept>
        <code value="ORPHA:91397" />
        <display value="Isolated ankyloblepharon filiforme adnatum" />
      </concept>
      <concept>
        <code value="ORPHA:91411" />
        <display value="Congenital ptosis" />
      </concept>
      <concept>
        <code value="ORPHA:91412" />
        <display value="Marcus-Gunn syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91413" />
        <display value="Congenital Horner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91414" />
        <display value="Pilomatrixoma" />
      </concept>
      <concept>
        <code value="ORPHA:91416" />
        <display value="Isolated congenital alacrima" />
      </concept>
      <concept>
        <code value="ORPHA:91481" />
        <display value="Ring dermoid of cornea" />
      </concept>
      <concept>
        <code value="ORPHA:91483" />
        <display value="Rieger anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:91489" />
        <display value="Isolated congenital megalocornea" />
      </concept>
      <concept>
        <code value="ORPHA:91490" />
        <display value="Isolated congenital sclerocornea" />
      </concept>
      <concept>
        <code value="ORPHA:91491" />
        <display value="Congenital ectropion uveae" />
      </concept>
      <concept>
        <code value="ORPHA:91492" />
        <display value="Early-onset non-syndromic cataract" />
      </concept>
      <concept>
        <code value="ORPHA:91494" />
        <display value="Macular coloboma-cleft palate-hallux valgus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91495" />
        <display value="Persistent hyperplastic primary vitreous" />
      </concept>
      <concept>
        <code value="ORPHA:91496" />
        <display value="Snowflake vitreoretinal degeneration" />
      </concept>
      <concept>
        <code value="ORPHA:91498" />
        <display value="Familial congenital palsy of trochlear nerve" />
      </concept>
      <concept>
        <code value="ORPHA:915" />
        <display value="Aarskog-Scott syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91500" />
        <display value="Tubulointerstitial nephritis and uveitis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:91546" />
        <display value="Lyme disease" />
      </concept>
      <concept>
        <code value="ORPHA:91547" />
        <display value="Relapsing fever" />
      </concept>
      <concept>
        <code value="ORPHA:916" />
        <display value="Aase-Smith syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:92" />
        <display value="Juvenile idiopathic arthritis" />
      </concept>
      <concept>
        <code value="ORPHA:920" />
        <display value="Ablepharon macrostomia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:92050" />
        <display value="Congenital tufting enteropathy" />
      </concept>
      <concept>
        <code value="ORPHA:921" />
        <display value="Abruzzo-Erickson syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:922" />
        <display value="Familial nasal acilia" />
      </concept>
      <concept>
        <code value="ORPHA:926" />
        <display value="Acatalasemia" />
      </concept>
      <concept>
        <code value="ORPHA:927" />
        <display value="Hyperammonemia due to N-acetylglutamate synthase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:929" />
        <display value="Achalasia-microcephaly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93" />
        <display value="Aspartylglucosaminuria" />
      </concept>
      <concept>
        <code value="ORPHA:930" />
        <display value="Idiopathic achalasia" />
      </concept>
      <concept>
        <code value="ORPHA:931" />
        <display value="Acheiropodia" />
      </concept>
      <concept>
        <code value="ORPHA:93100" />
        <display value="Renal agenesis, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:93101" />
        <display value="Renal hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93108" />
        <display value="Renal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93109" />
        <display value="Congenital megacalycosis" />
      </concept>
      <concept>
        <code value="ORPHA:93110" />
        <display value="Posterior urethral valve" />
      </concept>
      <concept>
        <code value="ORPHA:93111" />
        <display value="Renal cysts and diabetes syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93114" />
        <display value="Autosomal dominant intermediate Charcot-Marie-Tooth disease type E" />
      </concept>
      <concept>
        <code value="ORPHA:93126" />
        <display value="Pauci-immune glomerulonephritis" />
      </concept>
      <concept>
        <code value="ORPHA:93160" />
        <display value="Hypocalcemic vitamin D-resistant rickets" />
      </concept>
      <concept>
        <code value="ORPHA:93164" />
        <display value="Transient pseudohypoaldosteronism" />
      </concept>
      <concept>
        <code value="ORPHA:93172" />
        <display value="Renal dysplasia, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:93173" />
        <display value="Renal dysplasia, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:93176" />
        <display value="Unilateral congenital megacalycosis" />
      </concept>
      <concept>
        <code value="ORPHA:93177" />
        <display value="Congenital bilateral megacalycosis" />
      </concept>
      <concept>
        <code value="ORPHA:932" />
        <display value="Achondrogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:93206" />
        <display value="Idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis" />
      </concept>
      <concept>
        <code value="ORPHA:93207" />
        <display value="Idiopathic steroid-sensitive nephrotic syndrome with minimal change" />
      </concept>
      <concept>
        <code value="ORPHA:93209" />
        <display value="Idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation" />
      </concept>
      <concept>
        <code value="ORPHA:93213" />
        <display value="Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis" />
      </concept>
      <concept>
        <code value="ORPHA:93214" />
        <display value="Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation" />
      </concept>
      <concept>
        <code value="ORPHA:93216" />
        <display value="Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes" />
      </concept>
      <concept>
        <code value="ORPHA:93217" />
        <display value="Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:93218" />
        <display value="Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis" />
      </concept>
      <concept>
        <code value="ORPHA:93220" />
        <display value="Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:93221" />
        <display value="Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes" />
      </concept>
      <concept>
        <code value="ORPHA:93222" />
        <display value="Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation" />
      </concept>
      <concept>
        <code value="ORPHA:93256" />
        <display value="Fragile X-associated tremor/ataxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93258" />
        <display value="Pfeiffer syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:93259" />
        <display value="Pfeiffer syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93260" />
        <display value="Pfeiffer syndrome type 3" />
      </concept>
      <concept>
        <code value="ORPHA:93262" />
        <display value="Crouzon syndrome-acanthosis nigricans syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93267" />
        <display value="Cloverleaf skull-multiple congenital anomalies syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93268" />
        <display value="Short rib-polydactyly syndrome, Beemer-Langer type" />
      </concept>
      <concept>
        <code value="ORPHA:93269" />
        <display value="Short rib-polydactyly syndrome, Majewski type" />
      </concept>
      <concept>
        <code value="ORPHA:93270" />
        <display value="Short rib-polydactyly syndrome, Saldino-Noonan type" />
      </concept>
      <concept>
        <code value="ORPHA:93271" />
        <display value="Short rib-polydactyly syndrome, Verma-Naumoff type" />
      </concept>
      <concept>
        <code value="ORPHA:93274" />
        <display value="Thanatophoric dysplasia type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93276" />
        <display value="Polyostotic fibrous dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93277" />
        <display value="Monostotic fibrous dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93279" />
        <display value="Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis" />
      </concept>
      <concept>
        <code value="ORPHA:93282" />
        <display value="Spondyloepimetaphyseal dysplasia, PAPSS2 type" />
      </concept>
      <concept>
        <code value="ORPHA:93283" />
        <display value="Spondyloepiphyseal dysplasia, Kimberley type" />
      </concept>
      <concept>
        <code value="ORPHA:93284" />
        <display value="Spondyloepiphyseal dysplasia tarda" />
      </concept>
      <concept>
        <code value="ORPHA:93292" />
        <display value="Adenoma of the pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:93293" />
        <display value="Okihiro syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93296" />
        <display value="Achondrogenesis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93297" />
        <display value="Hypochondrogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:93298" />
        <display value="Achondrogenesis type 1B" />
      </concept>
      <concept>
        <code value="ORPHA:93299" />
        <display value="Achondrogenesis type 1A" />
      </concept>
      <concept>
        <code value="ORPHA:93302" />
        <display value="Brachyolmia, Maroteaux type" />
      </concept>
      <concept>
        <code value="ORPHA:93304" />
        <display value="Autosomal dominant brachyolmia" />
      </concept>
      <concept>
        <code value="ORPHA:93307" />
        <display value="Multiple epiphyseal dysplasia type 4" />
      </concept>
      <concept>
        <code value="ORPHA:93308" />
        <display value="Multiple epiphyseal dysplasia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:93311" />
        <display value="Multiple epiphyseal dysplasia type 5" />
      </concept>
      <concept>
        <code value="ORPHA:93314" />
        <display value="Spondylometaphyseal dysplasia, Kozlowski type" />
      </concept>
      <concept>
        <code value="ORPHA:93315" />
        <display value="Spondylometaphyseal dysplasia, corner fracture type" />
      </concept>
      <concept>
        <code value="ORPHA:93316" />
        <display value="Spondylometaphyseal dysplasia, Schmidt type" />
      </concept>
      <concept>
        <code value="ORPHA:93317" />
        <display value="Spondylometaphyseal dysplasia, Sedaghatian type" />
      </concept>
      <concept>
        <code value="ORPHA:93320" />
        <display value="Ulnar hemimelia" />
      </concept>
      <concept>
        <code value="ORPHA:93321" />
        <display value="Radial hemimelia" />
      </concept>
      <concept>
        <code value="ORPHA:93322" />
        <display value="Tibial hemimelia" />
      </concept>
      <concept>
        <code value="ORPHA:93323" />
        <display value="Fibular hemimelia" />
      </concept>
      <concept>
        <code value="ORPHA:93324" />
        <display value="Autosomal recessive Kenny-Caffey syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93325" />
        <display value="Autosomal dominant Kenny-Caffey syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93328" />
        <display value="Autosomal dominant omodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93329" />
        <display value="Autosomal recessive omodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93333" />
        <display value="Pelviscapular dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93334" />
        <display value="Postaxial polydactyly type A" />
      </concept>
      <concept>
        <code value="ORPHA:93335" />
        <display value="Postaxial polydactyly type B" />
      </concept>
      <concept>
        <code value="ORPHA:93336" />
        <display value="Polydactyly of a triphalangeal thumb" />
      </concept>
      <concept>
        <code value="ORPHA:93337" />
        <display value="Polydactyly of an index finger" />
      </concept>
      <concept>
        <code value="ORPHA:93338" />
        <display value="Polysyndactyly" />
      </concept>
      <concept>
        <code value="ORPHA:93339" />
        <display value="Polydactyly of a biphalangeal thumb" />
      </concept>
      <concept>
        <code value="ORPHA:93346" />
        <display value="Spondyloepimetaphyseal dysplasia congenita, Strudwick type" />
      </concept>
      <concept>
        <code value="ORPHA:93347" />
        <display value="Anauxetic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93349" />
        <display value="X-linked spondyloepimetaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93351" />
        <display value="Spondyloepimetaphyseal dysplasia, Irapa type" />
      </concept>
      <concept>
        <code value="ORPHA:93352" />
        <display value="Spondyloepimetaphyseal dysplasia, Shohat type" />
      </concept>
      <concept>
        <code value="ORPHA:93356" />
        <display value="Spondyloepimetaphyseal dysplasia, Missouri type" />
      </concept>
      <concept>
        <code value="ORPHA:93357" />
        <display value="SPONASTRIME dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93358" />
        <display value="Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93359" />
        <display value="Spondyloepimetaphyseal dysplasia with joint laxity" />
      </concept>
      <concept>
        <code value="ORPHA:93360" />
        <display value="Spondyloepimetaphyseal dysplasia with multiple dislocations" />
      </concept>
      <concept>
        <code value="ORPHA:93372" />
        <display value="Familial hypocalciuric hypercalcemia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:93382" />
        <display value="Brachydactyly type A6" />
      </concept>
      <concept>
        <code value="ORPHA:93383" />
        <display value="Brachydactyly type B" />
      </concept>
      <concept>
        <code value="ORPHA:93384" />
        <display value="Brachydactyly type C" />
      </concept>
      <concept>
        <code value="ORPHA:93387" />
        <display value="Brachydactyly type E" />
      </concept>
      <concept>
        <code value="ORPHA:93388" />
        <display value="Brachydactyly type A1" />
      </concept>
      <concept>
        <code value="ORPHA:93389" />
        <display value="Brachydactyly type A5" />
      </concept>
      <concept>
        <code value="ORPHA:93394" />
        <display value="Brachydactyly type A4" />
      </concept>
      <concept>
        <code value="ORPHA:93395" />
        <display value="Ballard syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93396" />
        <display value="Brachydactyly type A2" />
      </concept>
      <concept>
        <code value="ORPHA:93397" />
        <display value="Brachydactyly type A7" />
      </concept>
      <concept>
        <code value="ORPHA:93398" />
        <display value="Genochondromatosis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93399" />
        <display value="Juvenile sialidosis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93400" />
        <display value="Congenital sialidosis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93402" />
        <display value="Syndactyly type 1" />
      </concept>
      <concept>
        <code value="ORPHA:93403" />
        <display value="Syndactyly type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93404" />
        <display value="Syndactyly type 3" />
      </concept>
      <concept>
        <code value="ORPHA:93405" />
        <display value="Syndactyly type 4" />
      </concept>
      <concept>
        <code value="ORPHA:93406" />
        <display value="Syndactyly type 5" />
      </concept>
      <concept>
        <code value="ORPHA:93409" />
        <display value="Brachydactyly-syndactyly, Zhao type" />
      </concept>
      <concept>
        <code value="ORPHA:93419" />
        <display value="Rare bone disease" />
      </concept>
      <concept>
        <code value="ORPHA:93420" />
        <display value="FGFR3-related chondrodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93421" />
        <display value="Type 2 collagen-related bone disorder" />
      </concept>
      <concept>
        <code value="ORPHA:93422" />
        <display value="Type 11 collagen-related bone disorder" />
      </concept>
      <concept>
        <code value="ORPHA:93423" />
        <display value="Sulfation-related bone disorder" />
      </concept>
      <concept>
        <code value="ORPHA:93424" />
        <display value="Perlecan-related bone disorder" />
      </concept>
      <concept>
        <code value="ORPHA:93425" />
        <display value="Filamin-related bone disorder" />
      </concept>
      <concept>
        <code value="ORPHA:93426" />
        <display value="Ciliopathies with major skeletal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:93429" />
        <display value="Multiple epiphyseal dysplasia and pseudoachondroplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93430" />
        <display value="Multiple metaphyseal dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93434" />
        <display value="Spondylodysplastic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93436" />
        <display value="Acromelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93437" />
        <display value="Acromesomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93438" />
        <display value="Mesomelic and rhizo-mesomelic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93439" />
        <display value="Campomelic dysplasia and related disorders" />
      </concept>
      <concept>
        <code value="ORPHA:93440" />
        <display value="Slender bone dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93441" />
        <display value="Primary bone dysplasia with multiple joint dislocations" />
      </concept>
      <concept>
        <code value="ORPHA:93442" />
        <display value="Chondrodysplasia punctata" />
      </concept>
      <concept>
        <code value="ORPHA:93443" />
        <display value="Neonatal osteosclerotic dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93444" />
        <display value="Primary bone dysplasia with increased bone density" />
      </concept>
      <concept>
        <code value="ORPHA:93446" />
        <display value="Primary bone dysplasia with decreased bone density" />
      </concept>
      <concept>
        <code value="ORPHA:93447" />
        <display value="Primary bone dysplasia with defective bone mineralization" />
      </concept>
      <concept>
        <code value="ORPHA:93448" />
        <display value="Lysosomal storage disease with skeletal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:93449" />
        <display value="Primary osteolysis" />
      </concept>
      <concept>
        <code value="ORPHA:93450" />
        <display value="Primary bone dysplasia with disorganized development of skeletal components" />
      </concept>
      <concept>
        <code value="ORPHA:93451" />
        <display value="Cleidocranial dysplasia and isolated cranial ossification defect" />
      </concept>
      <concept>
        <code value="ORPHA:93453" />
        <display value="Dysostosis with predominant craniofacial involvement" />
      </concept>
      <concept>
        <code value="ORPHA:93454" />
        <display value="Dysostosis with predominant vertebral and costal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:93455" />
        <display value="Patellar dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:93457" />
        <display value="Non-syndromic limb reduction defect" />
      </concept>
      <concept>
        <code value="ORPHA:93458" />
        <display value="Non-syndromic polydactyly, syndactyly and/or hyperphalangy" />
      </concept>
      <concept>
        <code value="ORPHA:93459" />
        <display value="Syndrome with synostosis or other joint formation defect" />
      </concept>
      <concept>
        <code value="ORPHA:93460" />
        <display value="Overgrowth syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93461" />
        <display value="Chromosomal disease with overgrowth" />
      </concept>
      <concept>
        <code value="ORPHA:93465" />
        <display value="Lethal chondrodysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:93473" />
        <display value="Hurler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93474" />
        <display value="Scheie syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93476" />
        <display value="Hurler-Scheie syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:935" />
        <display value="Short-limb skeletal dysplasia with severe combined immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:93545" />
        <display value="Renal or urinary tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:93546" />
        <display value="Non-syndromic renal or urinary tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:93547" />
        <display value="Syndromic renal or urinary tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:93548" />
        <display value="Glomerular disease" />
      </concept>
      <concept>
        <code value="ORPHA:93550" />
        <display value="Basement membrane disease" />
      </concept>
      <concept>
        <code value="ORPHA:93551" />
        <display value="Secondary glomerular disease" />
      </concept>
      <concept>
        <code value="ORPHA:93552" />
        <display value="Pediatric systemic lupus erythematosus" />
      </concept>
      <concept>
        <code value="ORPHA:93554" />
        <display value="Type II mixed cryoglobulinemia" />
      </concept>
      <concept>
        <code value="ORPHA:93555" />
        <display value="Mixed cryoglobulinemia type III" />
      </concept>
      <concept>
        <code value="ORPHA:93556" />
        <display value="Heavy chain deposition disease" />
      </concept>
      <concept>
        <code value="ORPHA:93557" />
        <display value="Light and heavy chain deposition disease" />
      </concept>
      <concept>
        <code value="ORPHA:93558" />
        <display value="Light chain deposition disease" />
      </concept>
      <concept>
        <code value="ORPHA:93560" />
        <display value="AApoAI amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:93561" />
        <display value="ALys amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:93562" />
        <display value="AFib amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:93568" />
        <display value="Juvenile polymyositis" />
      </concept>
      <concept>
        <code value="ORPHA:93569" />
        <display value="Polymyalgia rheumatica" />
      </concept>
      <concept>
        <code value="ORPHA:93571" />
        <display value="Dense deposit disease" />
      </concept>
      <concept>
        <code value="ORPHA:93573" />
        <display value="Thrombotic microangiopathy" />
      </concept>
      <concept>
        <code value="ORPHA:93575" />
        <display value="Atypical hemolytic-uremic syndrome with C3 anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:93576" />
        <display value="Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:93578" />
        <display value="Atypical hemolytic-uremic syndrome with B factor anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:93579" />
        <display value="Atypical hemolytic-uremic syndrome with H factor anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:93580" />
        <display value="Atypical hemolytic-uremic syndrome with I factor anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:93581" />
        <display value="Atypical hemolytic-uremic syndrome with anti-factor H antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:93583" />
        <display value="Congenital thrombotic thrombocytopenic purpura" />
      </concept>
      <concept>
        <code value="ORPHA:93585" />
        <display value="Acquired thrombotic thrombocytopenic purpura" />
      </concept>
      <concept>
        <code value="ORPHA:93587" />
        <display value="Familial cystic renal disease" />
      </concept>
      <concept>
        <code value="ORPHA:93589" />
        <display value="Late-onset nephronophthisis" />
      </concept>
      <concept>
        <code value="ORPHA:93591" />
        <display value="Infantile nephronophthisis" />
      </concept>
      <concept>
        <code value="ORPHA:93592" />
        <display value="Juvenile nephronophthisis" />
      </concept>
      <concept>
        <code value="ORPHA:93593" />
        <display value="Nephropathy secondary to a storage or other metabolic disease" />
      </concept>
      <concept>
        <code value="ORPHA:93598" />
        <display value="Primary hyperoxaluria type 1" />
      </concept>
      <concept>
        <code value="ORPHA:93599" />
        <display value="Primary hyperoxaluria type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93600" />
        <display value="Primary hyperoxaluria type 3" />
      </concept>
      <concept>
        <code value="ORPHA:93601" />
        <display value="Xanthinuria type I" />
      </concept>
      <concept>
        <code value="ORPHA:93602" />
        <display value="Xanthinuria type II" />
      </concept>
      <concept>
        <code value="ORPHA:93603" />
        <display value="Rare renal tubular disease" />
      </concept>
      <concept>
        <code value="ORPHA:93604" />
        <display value="Antenatal Bartter syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93605" />
        <display value="Classic Bartter syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93606" />
        <display value="Nephrogenic syndrome of inappropriate antidiuresis" />
      </concept>
      <concept>
        <code value="ORPHA:93607" />
        <display value="Autosomal recessive proximal renal tubular acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:93608" />
        <display value="Autosomal dominant distal renal tubular acidosis" />
      </concept>
      <concept>
        <code value="ORPHA:93610" />
        <display value="Distal renal tubular acidosis with anemia" />
      </concept>
      <concept>
        <code value="ORPHA:93612" />
        <display value="Cystinuria type A" />
      </concept>
      <concept>
        <code value="ORPHA:93613" />
        <display value="Cystinuria type B" />
      </concept>
      <concept>
        <code value="ORPHA:93614" />
        <display value="Hematological disorder with renal involvement" />
      </concept>
      <concept>
        <code value="ORPHA:93616" />
        <display value="Hemoglobin H disease" />
      </concept>
      <concept>
        <code value="ORPHA:93618" />
        <display value="Rare cause of hypertension" />
      </concept>
      <concept>
        <code value="ORPHA:93619" />
        <display value="Rare renal tumor" />
      </concept>
      <concept>
        <code value="ORPHA:93622" />
        <display value="Dent disease type 1" />
      </concept>
      <concept>
        <code value="ORPHA:93623" />
        <display value="Dent disease type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93626" />
        <display value="Rare renal disease" />
      </concept>
      <concept>
        <code value="ORPHA:93665" />
        <display value="Autoinflammatory syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93672" />
        <display value="Juvenile dermatomyositis" />
      </concept>
      <concept>
        <code value="ORPHA:93682" />
        <display value="Pediatric Castleman disease" />
      </concept>
      <concept>
        <code value="ORPHA:93685" />
        <display value="Localized Castleman disease" />
      </concept>
      <concept>
        <code value="ORPHA:93686" />
        <display value="Multicentric Castleman disease" />
      </concept>
      <concept>
        <code value="ORPHA:93890" />
        <display value="Rare developmental defect during embryogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:939" />
        <display value="3-hydroxyisobutyric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:93921" />
        <display value="Neurofibromatosis type 3" />
      </concept>
      <concept>
        <code value="ORPHA:93924" />
        <display value="Lobar holoprosencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:93925" />
        <display value="Alobar holoprosencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:93926" />
        <display value="Midline interhemispheric variant of holoprosencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:93928" />
        <display value="Epispadias" />
      </concept>
      <concept>
        <code value="ORPHA:93929" />
        <display value="Cloacal exstrophy" />
      </concept>
      <concept>
        <code value="ORPHA:93930" />
        <display value="Bladder exstrophy" />
      </concept>
      <concept>
        <code value="ORPHA:93932" />
        <display value="FG syndrome type 1" />
      </concept>
      <concept>
        <code value="ORPHA:93938" />
        <display value="Laryngotracheoesophageal cleft type 1" />
      </concept>
      <concept>
        <code value="ORPHA:93939" />
        <display value="Laryngotracheoesophageal cleft type 2" />
      </concept>
      <concept>
        <code value="ORPHA:93940" />
        <display value="Laryngotracheoesophageal cleft type 3" />
      </concept>
      <concept>
        <code value="ORPHA:93941" />
        <display value="Laryngotracheoesophageal cleft type 4" />
      </concept>
      <concept>
        <code value="ORPHA:93942" />
        <display value="Superior celosomia" />
      </concept>
      <concept>
        <code value="ORPHA:93945" />
        <display value="X-linked intellectual disability, Porteous type" />
      </concept>
      <concept>
        <code value="ORPHA:93946" />
        <display value="Hamel cerebro-palato-cardiac syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93947" />
        <display value="X-linked intellectual disability, Golabi-Ito-Hall type" />
      </concept>
      <concept>
        <code value="ORPHA:93950" />
        <display value="X-linked intellectual disability, Sutherland-Haan type" />
      </concept>
      <concept>
        <code value="ORPHA:93951" />
        <display value="X-linked dominant intellectual disability-epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93952" />
        <display value="X-linked intellectual disability, Hedera type" />
      </concept>
      <concept>
        <code value="ORPHA:93953" />
        <display value="Familial thyroglossal duct cyst" />
      </concept>
      <concept>
        <code value="ORPHA:93958" />
        <display value="Oromandibular dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:93964" />
        <display value="Blepharospasm-oromandibular dystonia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93969" />
        <display value="Myelomeningocele" />
      </concept>
      <concept>
        <code value="ORPHA:93970" />
        <display value="Holmes-Gang syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93971" />
        <display value="Chudley-Lowry-Hoar syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93972" />
        <display value="Juberg-Marsidi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93973" />
        <display value="Carpenter-Waziri syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93974" />
        <display value="Smith-Fineman-Myers syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93975" />
        <display value="Renier-Gabreels-Jasper syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:93976" />
        <display value="Anotia" />
      </concept>
      <concept>
        <code value="ORPHA:94" />
        <display value="Astrocytoma" />
      </concept>
      <concept>
        <code value="ORPHA:94056" />
        <display value="Humero-ulnar synostosis" />
      </concept>
      <concept>
        <code value="ORPHA:94058" />
        <display value="Neovascular glaucoma" />
      </concept>
      <concept>
        <code value="ORPHA:94063" />
        <display value="12q14 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:94064" />
        <display value="Deafness-infertility syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:94065" />
        <display value="15q24 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:94066" />
        <display value="Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:94068" />
        <display value="Spondyloepiphyseal dysplasia congenita" />
      </concept>
      <concept>
        <code value="ORPHA:94075" />
        <display value="Severe immune-mediated enteropathy" />
      </concept>
      <concept>
        <code value="ORPHA:94080" />
        <display value="Non-functioning paraganglioma" />
      </concept>
      <concept>
        <code value="ORPHA:94083" />
        <display value="Partington syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:94086" />
        <display value="Blue diaper syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:94087" />
        <display value="Cytophagic histiocytic panniculitis" />
      </concept>
      <concept>
        <code value="ORPHA:94088" />
        <display value="Hereditary renal hypouricemia" />
      </concept>
      <concept>
        <code value="ORPHA:94089" />
        <display value="Pseudohypoparathyroidism type 1B" />
      </concept>
      <concept>
        <code value="ORPHA:94090" />
        <display value="Pseudohypoparathyroidism type 2" />
      </concept>
      <concept>
        <code value="ORPHA:94093" />
        <display value="Neuroleptic malignant syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:94095" />
        <display value="Spondylocostal dysostosis-anal atresia-genitourinary malformation syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:941" />
        <display value="D-glyceric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:94122" />
        <display value="Cerebellar ataxia, Cayman type" />
      </concept>
      <concept>
        <code value="ORPHA:94124" />
        <display value="Spinocerebellar ataxia with axonal neuropathy type 1" />
      </concept>
      <concept>
        <code value="ORPHA:94125" />
        <display value="Recessive mitochondrial ataxia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:94145" />
        <display value="Autosomal dominant cerebellar ataxia type I" />
      </concept>
      <concept>
        <code value="ORPHA:94147" />
        <display value="Spinocerebellar ataxia type 7" />
      </concept>
      <concept>
        <code value="ORPHA:94148" />
        <display value="Autosomal dominant cerebellar ataxia type III" />
      </concept>
      <concept>
        <code value="ORPHA:94149" />
        <display value="Autosomal dominant cerebellar ataxia type IV" />
      </concept>
      <concept>
        <code value="ORPHA:94150" />
        <display value="Anonychia congenita totalis" />
      </concept>
      <concept>
        <code value="ORPHA:943" />
        <display value="Malonic aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:945" />
        <display value="Acalvaria" />
      </concept>
      <concept>
        <code value="ORPHA:946" />
        <display value="Acrocephalosyndactyly" />
      </concept>
      <concept>
        <code value="ORPHA:949" />
        <display value="Acrocraniofacial dysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:95" />
        <display value="Friedreich ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:950" />
        <display value="Acrodysostosis" />
      </concept>
      <concept>
        <code value="ORPHA:95157" />
        <display value="Acute hepatic porphyria" />
      </concept>
      <concept>
        <code value="ORPHA:95159" />
        <display value="Hepatoerythropoietic porphyria" />
      </concept>
      <concept>
        <code value="ORPHA:95161" />
        <display value="Chronic hepatic porphyria" />
      </concept>
      <concept>
        <code value="ORPHA:952" />
        <display value="Acrofacial dysostosis, Weyers type" />
      </concept>
      <concept>
        <code value="ORPHA:95232" />
        <display value="Lissencephaly due to LIS1 mutation" />
      </concept>
      <concept>
        <code value="ORPHA:95409" />
        <display value="Acute adrenal insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:95427" />
        <display value="Secondary short bowel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:95428" />
        <display value="COG8-CDG" />
      </concept>
      <concept>
        <code value="ORPHA:95429" />
        <display value="Angioma serpiginosum" />
      </concept>
      <concept>
        <code value="ORPHA:95430" />
        <display value="Congenital tracheomalacia" />
      </concept>
      <concept>
        <code value="ORPHA:95431" />
        <display value="Twin to twin transfusion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:95432" />
        <display value="Primary progressive aphasia" />
      </concept>
      <concept>
        <code value="ORPHA:95433" />
        <display value="Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:95434" />
        <display value="Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:95443" />
        <display value="Mesocardia" />
      </concept>
      <concept>
        <code value="ORPHA:95448" />
        <display value="Aortic valve atresia" />
      </concept>
      <concept>
        <code value="ORPHA:95449" />
        <display value="Congenital aortic valve insufficiency" />
      </concept>
      <concept>
        <code value="ORPHA:95455" />
        <display value="Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum" />
      </concept>
      <concept>
        <code value="ORPHA:95457" />
        <display value="Tricuspid valve agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:95458" />
        <display value="Tricuspid valve prolapse" />
      </concept>
      <concept>
        <code value="ORPHA:95459" />
        <display value="Congenital tricuspid stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:95461" />
        <display value="Straddling or overriding tricuspid valve" />
      </concept>
      <concept>
        <code value="ORPHA:95462" />
        <display value="Accessory tricuspid valve tissue" />
      </concept>
      <concept>
        <code value="ORPHA:95463" />
        <display value="Anomaly of the tricuspid subvalvular apparatus" />
      </concept>
      <concept>
        <code value="ORPHA:95464" />
        <display value="Congenital mitral valve insufficiency and/or stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:95465" />
        <display value="Cleft mitral valve" />
      </concept>
      <concept>
        <code value="ORPHA:95474" />
        <display value="Double-orifice mitral valve" />
      </concept>
      <concept>
        <code value="ORPHA:95483" />
        <display value="Univentricular cardiopathy" />
      </concept>
      <concept>
        <code value="ORPHA:95484" />
        <display value="Aneurysm or dilatation of ascending aorta" />
      </concept>
      <concept>
        <code value="ORPHA:95485" />
        <display value="Arterial duct anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:95486" />
        <display value="Premature closure of the arterial duct" />
      </concept>
      <concept>
        <code value="ORPHA:95488" />
        <display value="Non-acquired pituitary hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:95491" />
        <display value="Congenital coronary artery aneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:95493" />
        <display value="Abnormal origin or aberrant course of coronary artery" />
      </concept>
      <concept>
        <code value="ORPHA:95494" />
        <display value="Combined pituitary hormone deficiencies, genetic forms" />
      </concept>
      <concept>
        <code value="ORPHA:95495" />
        <display value="Disease associated with non-acquired combined pituitary hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:95496" />
        <display value="Pituitary stalk interruption syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:95498" />
        <display value="Congenital anomaly of superior vena cava" />
      </concept>
      <concept>
        <code value="ORPHA:95499" />
        <display value="Congenital anomaly of the inferior vena cava" />
      </concept>
      <concept>
        <code value="ORPHA:955" />
        <display value="Acroosteolysis dominant type" />
      </concept>
      <concept>
        <code value="ORPHA:95500" />
        <display value="Congenital anomaly of the coronary sinus" />
      </concept>
      <concept>
        <code value="ORPHA:95502" />
        <display value="Acquired pituitary hormone deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:95503" />
        <display value="Pituitary hormone deficiency from tumoral origin" />
      </concept>
      <concept>
        <code value="ORPHA:95505" />
        <display value="Pituitary hormone deficiency from meningeal origin" />
      </concept>
      <concept>
        <code value="ORPHA:95506" />
        <display value="Primary hypophysitis" />
      </concept>
      <concept>
        <code value="ORPHA:95507" />
        <display value="Congenital anomaly of hepatic vein" />
      </concept>
      <concept>
        <code value="ORPHA:95510" />
        <display value="Atrial appendage anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:95512" />
        <display value="Adenohypophysitis" />
      </concept>
      <concept>
        <code value="ORPHA:95513" />
        <display value="Panhypophysitis" />
      </concept>
      <concept>
        <code value="ORPHA:95611" />
        <display value="Pituitary hormone defiency from vascular origin" />
      </concept>
      <concept>
        <code value="ORPHA:95613" />
        <display value="Pituitary apoplexy" />
      </concept>
      <concept>
        <code value="ORPHA:95617" />
        <display value="Pituitary hormone deficiency secondary to a granulomatous disease" />
      </concept>
      <concept>
        <code value="ORPHA:95618" />
        <display value="Pituitary hormone deficiency secondary to storage disease" />
      </concept>
      <concept>
        <code value="ORPHA:95619" />
        <display value="Iatrogenic or traumatic pituitary deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:95626" />
        <display value="Acquired central diabetes insipidus" />
      </concept>
      <concept>
        <code value="ORPHA:95699" />
        <display value="Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:957" />
        <display value="Acropectorovertebral dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:95700" />
        <display value="Familial adrenal hypoplasia with absent pituitary luteinizing hormone" />
      </concept>
      <concept>
        <code value="ORPHA:95702" />
        <display value="Cytomegalic congenital adrenal hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:95706" />
        <display value="Posterior hypospadias" />
      </concept>
      <concept>
        <code value="ORPHA:95707" />
        <display value="Isolated micropenis" />
      </concept>
      <concept>
        <code value="ORPHA:95708" />
        <display value="Precocious puberty" />
      </concept>
      <concept>
        <code value="ORPHA:95709" />
        <display value="Acquired premature ovarian failure" />
      </concept>
      <concept>
        <code value="ORPHA:95710" />
        <display value="Non-acquired premature ovarian failure" />
      </concept>
      <concept>
        <code value="ORPHA:95711" />
        <display value="Congenital hypothyroidism due to developmental anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:95712" />
        <display value="Thyroid ectopia" />
      </concept>
      <concept>
        <code value="ORPHA:95713" />
        <display value="Athyreosis" />
      </concept>
      <concept>
        <code value="ORPHA:95714" />
        <display value="Primary congenital hypothyroidism without thyroid developmental anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:95715" />
        <display value="Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies" />
      </concept>
      <concept>
        <code value="ORPHA:95716" />
        <display value="Familial thyroid dyshormonogenesis" />
      </concept>
      <concept>
        <code value="ORPHA:95717" />
        <display value="Idiopathic congenital hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:95718" />
        <display value="Congenital thyroid malformation without hypothyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:95719" />
        <display value="Thyroid hemiagenesis" />
      </concept>
      <concept>
        <code value="ORPHA:95720" />
        <display value="Thyroid hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:958" />
        <display value="Acro-renal-mandibular syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:95854" />
        <display value="Levocardia" />
      </concept>
      <concept>
        <code value="ORPHA:959" />
        <display value="Acro-renal-ocular syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96" />
        <display value="Ataxia with vitamin E deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:96055" />
        <display value="Tetrasomy 21" />
      </concept>
      <concept>
        <code value="ORPHA:96059" />
        <display value="Mosaic trisomy 4" />
      </concept>
      <concept>
        <code value="ORPHA:96060" />
        <display value="Mosaic trisomy 5" />
      </concept>
      <concept>
        <code value="ORPHA:96061" />
        <display value="Mosaic trisomy 8" />
      </concept>
      <concept>
        <code value="ORPHA:96063" />
        <display value="Mosaic trisomy 10" />
      </concept>
      <concept>
        <code value="ORPHA:96068" />
        <display value="Mosaic trisomy 22" />
      </concept>
      <concept>
        <code value="ORPHA:96069" />
        <display value="Distal trisomy 1p36" />
      </concept>
      <concept>
        <code value="ORPHA:96070" />
        <display value="Distal trisomy 2p" />
      </concept>
      <concept>
        <code value="ORPHA:96071" />
        <display value="Distal trisomy 3p" />
      </concept>
      <concept>
        <code value="ORPHA:96072" />
        <display value="4p16.3 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96074" />
        <display value="Distal trisomy 7p" />
      </concept>
      <concept>
        <code value="ORPHA:96076" />
        <display value="Beckwith-Wiedemann syndrome due to 11p15 microduplication" />
      </concept>
      <concept>
        <code value="ORPHA:96078" />
        <display value="16p13.3 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96092" />
        <display value="8p inverted duplication/deletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96094" />
        <display value="Distal trisomy 2q" />
      </concept>
      <concept>
        <code value="ORPHA:96095" />
        <display value="3q26 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96096" />
        <display value="Distal trisomy 4q" />
      </concept>
      <concept>
        <code value="ORPHA:96097" />
        <display value="Distal trisomy 5q" />
      </concept>
      <concept>
        <code value="ORPHA:96098" />
        <display value="Distal trisomy 6q" />
      </concept>
      <concept>
        <code value="ORPHA:96100" />
        <display value="Distal trisomy 8q" />
      </concept>
      <concept>
        <code value="ORPHA:96101" />
        <display value="Distal trisomy 9q" />
      </concept>
      <concept>
        <code value="ORPHA:96102" />
        <display value="Distal trisomy 10q" />
      </concept>
      <concept>
        <code value="ORPHA:96103" />
        <display value="Distal trisomy 11q" />
      </concept>
      <concept>
        <code value="ORPHA:96105" />
        <display value="Distal trisomy 13q" />
      </concept>
      <concept>
        <code value="ORPHA:96106" />
        <display value="Distal trisomy 16q" />
      </concept>
      <concept>
        <code value="ORPHA:96107" />
        <display value="Distal trisomy 20q" />
      </concept>
      <concept>
        <code value="ORPHA:96109" />
        <display value="Distal trisomy 22q" />
      </concept>
      <concept>
        <code value="ORPHA:96112" />
        <display value="Non-distal trisomy 9q" />
      </concept>
      <concept>
        <code value="ORPHA:96121" />
        <display value="7q11.23 microduplication syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96123" />
        <display value="Monosomy 22" />
      </concept>
      <concept>
        <code value="ORPHA:96125" />
        <display value="Distal monosomy 6p" />
      </concept>
      <concept>
        <code value="ORPHA:96126" />
        <display value="Distal monosomy 7p" />
      </concept>
      <concept>
        <code value="ORPHA:96129" />
        <display value="Distal monosomy 19p13.3" />
      </concept>
      <concept>
        <code value="ORPHA:96136" />
        <display value="Non-distal monosomy 7p" />
      </concept>
      <concept>
        <code value="ORPHA:96145" />
        <display value="Distal monosomy 4q" />
      </concept>
      <concept>
        <code value="ORPHA:96147" />
        <display value="Kleefstra syndrome due to 9q34 microdeletion" />
      </concept>
      <concept>
        <code value="ORPHA:96148" />
        <display value="Distal monosomy 10q" />
      </concept>
      <concept>
        <code value="ORPHA:96149" />
        <display value="Distal monosomy 12q" />
      </concept>
      <concept>
        <code value="ORPHA:96150" />
        <display value="Distal monosomy 14q" />
      </concept>
      <concept>
        <code value="ORPHA:96152" />
        <display value="Distal monosomy 20q" />
      </concept>
      <concept>
        <code value="ORPHA:96160" />
        <display value="Non-distal monosomy 12q" />
      </concept>
      <concept>
        <code value="ORPHA:96164" />
        <display value="Non-distal monosomy 20q" />
      </concept>
      <concept>
        <code value="ORPHA:96167" />
        <display value="Recombinant 8 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96168" />
        <display value="Monosomy 13q34" />
      </concept>
      <concept>
        <code value="ORPHA:96169" />
        <display value="Koolen-De Vries syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96170" />
        <display value="Emanuel syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96171" />
        <display value="Ring chromosome 2 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96172" />
        <display value="Ring chromosome 3 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96173" />
        <display value="Ring chromosome 9 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96175" />
        <display value="Ring chromosome 11 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96176" />
        <display value="Ring chromosome 13 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96177" />
        <display value="Ring chromosome 15 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96178" />
        <display value="Ring chromosome 16 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96179" />
        <display value="Maternal uniparental disomy of chromosome 2" />
      </concept>
      <concept>
        <code value="ORPHA:96180" />
        <display value="Maternal uniparental disomy of chromosome 4" />
      </concept>
      <concept>
        <code value="ORPHA:96181" />
        <display value="Maternal uniparental disomy of chromosome 6" />
      </concept>
      <concept>
        <code value="ORPHA:96182" />
        <display value="Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7" />
      </concept>
      <concept>
        <code value="ORPHA:96183" />
        <display value="Maternal uniparental disomy of chromosome 9" />
      </concept>
      <concept>
        <code value="ORPHA:96184" />
        <display value="Temple syndrome due to maternal uniparental disomy of chromosome 14" />
      </concept>
      <concept>
        <code value="ORPHA:96185" />
        <display value="Maternal uniparental disomy of chromosome 16" />
      </concept>
      <concept>
        <code value="ORPHA:96186" />
        <display value="Maternal uniparental disomy of chromosome 20" />
      </concept>
      <concept>
        <code value="ORPHA:96187" />
        <display value="Maternal uniparental disomy of chromosome 21" />
      </concept>
      <concept>
        <code value="ORPHA:96188" />
        <display value="Maternal uniparental disomy of chromosome 22" />
      </concept>
      <concept>
        <code value="ORPHA:96190" />
        <display value="Paternal uniparental disomy of chromosome 5" />
      </concept>
      <concept>
        <code value="ORPHA:96191" />
        <display value="Paternal uniparental disomy of chromosome 6" />
      </concept>
      <concept>
        <code value="ORPHA:96192" />
        <display value="Paternal uniparental disomy of chromosome 7" />
      </concept>
      <concept>
        <code value="ORPHA:96193" />
        <display value="Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11" />
      </concept>
      <concept>
        <code value="ORPHA:96194" />
        <display value="Paternal uniparental disomy of chromosome 20" />
      </concept>
      <concept>
        <code value="ORPHA:96195" />
        <display value="Paternal uniparental disomy of chromosome 21" />
      </concept>
      <concept>
        <code value="ORPHA:96201" />
        <display value="X small rings" />
      </concept>
      <concept>
        <code value="ORPHA:96253" />
        <display value="Cushing disease" />
      </concept>
      <concept>
        <code value="ORPHA:96256" />
        <display value="Somatotropic adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:96263" />
        <display value="48,XXXY syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96264" />
        <display value="49,XXXXY syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:96265" />
        <display value="Leydig cell hypoplasia due to complete LH resistance" />
      </concept>
      <concept>
        <code value="ORPHA:96266" />
        <display value="Leydig cell hypoplasia due to partial LH resistance" />
      </concept>
      <concept>
        <code value="ORPHA:96269" />
        <display value="Isolated partial vaginal agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:963" />
        <display value="Acromegaly" />
      </concept>
      <concept>
        <code value="ORPHA:96321" />
        <display value="Polyploidy" />
      </concept>
      <concept>
        <code value="ORPHA:96325" />
        <display value="Isochromosome Y" />
      </concept>
      <concept>
        <code value="ORPHA:96333" />
        <display value="Rare otorhinolaryngological malformation" />
      </concept>
      <concept>
        <code value="ORPHA:96334" />
        <display value="Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14" />
      </concept>
      <concept>
        <code value="ORPHA:96344" />
        <display value="Rare gynecologic or obstetric disease" />
      </concept>
      <concept>
        <code value="ORPHA:96346" />
        <display value="Anorectal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:96369" />
        <display value="Early-onset schizophrenia" />
      </concept>
      <concept>
        <code value="ORPHA:965" />
        <display value="Acromegaloid facial appearance syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:966" />
        <display value="Hypertrichosis-acromegaloid facial appearance syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:968" />
        <display value="Acromesomelic dysplasia, Hunter-Thompson type" />
      </concept>
      <concept>
        <code value="ORPHA:969" />
        <display value="Acromicric dysplasia" />
      </concept>
      <concept>
        <code value="ORPHA:97" />
        <display value="Familial paroxysmal ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:970" />
        <display value="Hereditary sensory and autonomic neuropathy type 2" />
      </concept>
      <concept>
        <code value="ORPHA:971" />
        <display value="Acrorenal syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97120" />
        <display value="Distal arthrogryposis" />
      </concept>
      <concept>
        <code value="ORPHA:972" />
        <display value="Hereditary continuous muscle fiber activity" />
      </concept>
      <concept>
        <code value="ORPHA:97214" />
        <display value="Eisenmenger syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97229" />
        <display value="Riboflavin transporter deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:97230" />
        <display value="Solar urticaria" />
      </concept>
      <concept>
        <code value="ORPHA:97231" />
        <display value="Ligneous conjunctivitis" />
      </concept>
      <concept>
        <code value="ORPHA:97232" />
        <display value="Fingerprint body myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:97234" />
        <display value="Glycogen storage disease due to phosphoglycerate mutase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:97238" />
        <display value="Rippling muscle disease" />
      </concept>
      <concept>
        <code value="ORPHA:97239" />
        <display value="Reducing body myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:97240" />
        <display value="Zebra body myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:97242" />
        <display value="Congenital muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:97244" />
        <display value="Rigid spine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97245" />
        <display value="Congenital myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:97249" />
        <display value="Pontocerebellar hypoplasia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:97252" />
        <display value="Mega-cisterna magna" />
      </concept>
      <concept>
        <code value="ORPHA:97253" />
        <display value="Neuroendocrine tumor of pancreas" />
      </concept>
      <concept>
        <code value="ORPHA:97261" />
        <display value="GRFoma" />
      </concept>
      <concept>
        <code value="ORPHA:97275" />
        <display value="Encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:97278" />
        <display value="PPoma" />
      </concept>
      <concept>
        <code value="ORPHA:97279" />
        <display value="Insulinoma" />
      </concept>
      <concept>
        <code value="ORPHA:97280" />
        <display value="Glucagonoma" />
      </concept>
      <concept>
        <code value="ORPHA:97282" />
        <display value="VIPoma" />
      </concept>
      <concept>
        <code value="ORPHA:97283" />
        <display value="Somatostatinoma" />
      </concept>
      <concept>
        <code value="ORPHA:97285" />
        <display value="Thyroid lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:97286" />
        <display value="Carney-Stratakis syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97287" />
        <display value="Bronchial neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:97289" />
        <display value="Thymic neuroendocrine tumor" />
      </concept>
      <concept>
        <code value="ORPHA:97290" />
        <display value="Familial papillary thyroid carcinoma with renal papillary neoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:97293" />
        <display value="Rare benign ovarian tumor" />
      </concept>
      <concept>
        <code value="ORPHA:97297" />
        <display value="Bohring-Opitz syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:973" />
        <display value="Congenital absence/hypoplasia of fingers excluding thumb, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:97330" />
        <display value="Thoracic outlet syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97332" />
        <display value="Kienbock disease" />
      </concept>
      <concept>
        <code value="ORPHA:97335" />
        <display value="Osgood-Schlatter disease" />
      </concept>
      <concept>
        <code value="ORPHA:97336" />
        <display value="Panner disease" />
      </concept>
      <concept>
        <code value="ORPHA:97337" />
        <display value="Sinding-Larsen-Johansson disease" />
      </concept>
      <concept>
        <code value="ORPHA:97338" />
        <display value="Melanoma of soft tissue" />
      </concept>
      <concept>
        <code value="ORPHA:97339" />
        <display value="Dural sinus malformation" />
      </concept>
      <concept>
        <code value="ORPHA:97340" />
        <display value="Hunter-McAlpine craniosynostosis" />
      </concept>
      <concept>
        <code value="ORPHA:97341" />
        <display value="Persistent placoid maculopathy" />
      </concept>
      <concept>
        <code value="ORPHA:97345" />
        <display value="ABri amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:97346" />
        <display value="ADan amyloidosis" />
      </concept>
      <concept>
        <code value="ORPHA:97349" />
        <display value="Postencephalitic parkinsonism" />
      </concept>
      <concept>
        <code value="ORPHA:97352" />
        <display value="Pellagra" />
      </concept>
      <concept>
        <code value="ORPHA:97353" />
        <display value="Dementia pugilistica" />
      </concept>
      <concept>
        <code value="ORPHA:97355" />
        <display value="Parkinsonism with dementia of Guadeloupe" />
      </concept>
      <concept>
        <code value="ORPHA:97360" />
        <display value="Robinow syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97361" />
        <display value="Renal hypoplasia, unilateral" />
      </concept>
      <concept>
        <code value="ORPHA:97362" />
        <display value="Renal hypoplasia, bilateral" />
      </concept>
      <concept>
        <code value="ORPHA:97363" />
        <display value="Unilateral multicystic dysplastic kidney" />
      </concept>
      <concept>
        <code value="ORPHA:97364" />
        <display value="Bilateral multicystic dysplastic kidney" />
      </concept>
      <concept>
        <code value="ORPHA:97366" />
        <display value="Multiloculated renal cyst" />
      </concept>
      <concept>
        <code value="ORPHA:97367" />
        <display value="Renal tubular dysgenesis due to twin-twin transfusion" />
      </concept>
      <concept>
        <code value="ORPHA:97368" />
        <display value="Drug-related renal tubular dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:97369" />
        <display value="Renal tubular dysgenesis of genetic origin" />
      </concept>
      <concept>
        <code value="ORPHA:974" />
        <display value="Adams-Oliver syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97548" />
        <display value="Ivemark syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97555" />
        <display value="Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:97556" />
        <display value="Congenital and infantile nephrotic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97560" />
        <display value="Idiopathic membranous glomerulonephritis" />
      </concept>
      <concept>
        <code value="ORPHA:97563" />
        <display value="Pauci-immune glomerulonephritis with ANCA" />
      </concept>
      <concept>
        <code value="ORPHA:97564" />
        <display value="Pauci-immune glomerulonephritis without ANCA" />
      </concept>
      <concept>
        <code value="ORPHA:97566" />
        <display value="Non-amyloid fibrillary glomerulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:97567" />
        <display value="Immunotactoid glomerulopathy" />
      </concept>
      <concept>
        <code value="ORPHA:97593" />
        <display value="Pseudohypoparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:97598" />
        <display value="Congenital renal artery stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:976" />
        <display value="Adenine phosphoribosyltransferase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:97678" />
        <display value="Maternal uniparental disomy of chromosome 13" />
      </concept>
      <concept>
        <code value="ORPHA:97685" />
        <display value="17q11 microdeletion syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:977" />
        <display value="Adrenomyodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:978" />
        <display value="ADULT syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:97927" />
        <display value="Peripheral resistance to thyroid hormones" />
      </concept>
      <concept>
        <code value="ORPHA:97929" />
        <display value="Rare cardiac disease" />
      </concept>
      <concept>
        <code value="ORPHA:97935" />
        <display value="Rare gastroenterologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:97944" />
        <display value="Gastroduodenal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:97945" />
        <display value="Intestinal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:97955" />
        <display value="Rare respiratory disease" />
      </concept>
      <concept>
        <code value="ORPHA:97957" />
        <display value="Respiratory or thoracic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:97962" />
        <display value="Rare surgical thoracic disease" />
      </concept>
      <concept>
        <code value="ORPHA:97965" />
        <display value="Rare surgical cardiac disease" />
      </concept>
      <concept>
        <code value="ORPHA:97966" />
        <display value="Rare ophthalmic disorder" />
      </concept>
      <concept>
        <code value="ORPHA:97978" />
        <display value="Rare endocrine disease" />
      </concept>
      <concept>
        <code value="ORPHA:97992" />
        <display value="Rare hematologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:98" />
        <display value="Autosomal recessive spastic ataxia of Charlevoix-Saguenay" />
      </concept>
      <concept>
        <code value="ORPHA:980" />
        <display value="Absence of the pulmonary artery" />
      </concept>
      <concept>
        <code value="ORPHA:98004" />
        <display value="Rare immune disease" />
      </concept>
      <concept>
        <code value="ORPHA:98006" />
        <display value="Rare neurologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:98010" />
        <display value="Infectious disease of the nervous system" />
      </concept>
      <concept>
        <code value="ORPHA:98022" />
        <display value="Rare headache" />
      </concept>
      <concept>
        <code value="ORPHA:98023" />
        <display value="Rare systemic or rheumatologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:98026" />
        <display value="Rare odontologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:98027" />
        <display value="Rare disease with odontological manifestation" />
      </concept>
      <concept>
        <code value="ORPHA:98028" />
        <display value="Rare circulatory system disease" />
      </concept>
      <concept>
        <code value="ORPHA:98033" />
        <display value="Rare neurologic disease with psychiatric involvement" />
      </concept>
      <concept>
        <code value="ORPHA:98036" />
        <display value="Rare otorhinolaryngologic disease" />
      </concept>
      <concept>
        <code value="ORPHA:98038" />
        <display value="Cranial malformation" />
      </concept>
      <concept>
        <code value="ORPHA:98039" />
        <display value="Digestive tract malformation" />
      </concept>
      <concept>
        <code value="ORPHA:98041" />
        <display value="Visceral malformation of the liver, biliary tract, pancreas or spleen" />
      </concept>
      <concept>
        <code value="ORPHA:98043" />
        <display value="Diaphragmatic or abdominal wall malformation" />
      </concept>
      <concept>
        <code value="ORPHA:98044" />
        <display value="Central nervous system malformation" />
      </concept>
      <concept>
        <code value="ORPHA:98045" />
        <display value="Respiratory or mediastinal malformation" />
      </concept>
      <concept>
        <code value="ORPHA:98047" />
        <display value="Rare infertility" />
      </concept>
      <concept>
        <code value="ORPHA:98048" />
        <display value="Rare male infertility" />
      </concept>
      <concept>
        <code value="ORPHA:98049" />
        <display value="Rare female infertility" />
      </concept>
      <concept>
        <code value="ORPHA:98050" />
        <display value="Rare allergic disease" />
      </concept>
      <concept>
        <code value="ORPHA:98052" />
        <display value="Rare allergic respiratory disease" />
      </concept>
      <concept>
        <code value="ORPHA:98053" />
        <display value="Rare genetic disease" />
      </concept>
      <concept>
        <code value="ORPHA:98054" />
        <display value="Rare genetic cardiac disease" />
      </concept>
      <concept>
        <code value="ORPHA:98056" />
        <display value="Rare genetic renal disease" />
      </concept>
      <concept>
        <code value="ORPHA:98057" />
        <display value="Rare tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98058" />
        <display value="Rare urinary tract tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98059" />
        <display value="Rare digestive tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98060" />
        <display value="Rare respiratory tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98061" />
        <display value="Rare otorhinolaryngologic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98062" />
        <display value="Rare nervous system tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98063" />
        <display value="Rare gynecological tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98074" />
        <display value="Gonadal dysgenesis of gynecological interest" />
      </concept>
      <concept>
        <code value="ORPHA:98078" />
        <display value="46,XX disorder of sex development induced by androgens excess" />
      </concept>
      <concept>
        <code value="ORPHA:98085" />
        <display value="46,XY disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:98086" />
        <display value="46,XY disorder of sex development due to a defect in testosterone metabolism by peripheral tissue" />
      </concept>
      <concept>
        <code value="ORPHA:98087" />
        <display value="Syndrome with 46,XY disorder of sex development" />
      </concept>
      <concept>
        <code value="ORPHA:98095" />
        <display value="Autosomal recessive congenital cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:98096" />
        <display value="Autosomal recessive metabolic cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:98097" />
        <display value="Autosomal recessive cerebellar ataxia due to a DNA repair defect" />
      </concept>
      <concept>
        <code value="ORPHA:98098" />
        <display value="Autosomal recessive degenerative and progressive cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:98099" />
        <display value="Autosomal recessive syndromic cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:981" />
        <display value="Internal carotid agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:98127" />
        <display value="Autosomal anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98130" />
        <display value="Autosomal trisomy" />
      </concept>
      <concept>
        <code value="ORPHA:98131" />
        <display value="Total autosomal trisomy" />
      </concept>
      <concept>
        <code value="ORPHA:98132" />
        <display value="Partial autosomal trisomy/tetrasomy" />
      </concept>
      <concept>
        <code value="ORPHA:98141" />
        <display value="Total autosomal monosomy" />
      </concept>
      <concept>
        <code value="ORPHA:98142" />
        <display value="Partial autosomal monosomy" />
      </concept>
      <concept>
        <code value="ORPHA:98152" />
        <display value="Autosomal uniparental disomy" />
      </concept>
      <concept>
        <code value="ORPHA:98153" />
        <display value="Maternal uniparental disomy" />
      </concept>
      <concept>
        <code value="ORPHA:98154" />
        <display value="Paternal uniparental disomy" />
      </concept>
      <concept>
        <code value="ORPHA:98155" />
        <display value="Gonosome anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98156" />
        <display value="Gonosome number anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98157" />
        <display value="Gonosome structural anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98158" />
        <display value="Chromosome Y structural anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98159" />
        <display value="Chromosome X structural anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98196" />
        <display value="Malformation syndrome with hamartosis" />
      </concept>
      <concept>
        <code value="ORPHA:982" />
        <display value="Pulmonary valve agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:98203" />
        <display value="Combined dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:98249" />
        <display value="Ehlers-Danlos syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98252" />
        <display value="Infectious encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:98253" />
        <display value="Postinfectious encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:98255" />
        <display value="Chronic encephalitis" />
      </concept>
      <concept>
        <code value="ORPHA:98257" />
        <display value="Neonatal epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98258" />
        <display value="Infantile epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98259" />
        <display value="Childhood-onset epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98260" />
        <display value="Adolescent-onset epilepsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98261" />
        <display value="Progressive myoclonic epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:98267" />
        <display value="Genetic non-syndromic obesity" />
      </concept>
      <concept>
        <code value="ORPHA:98274" />
        <display value="Myeloproliferative neoplasm" />
      </concept>
      <concept>
        <code value="ORPHA:98275" />
        <display value="Myelodysplastic/myeloproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:98277" />
        <display value="Acute myeloid leukemia with recurrent genetic anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98282" />
        <display value="Plasma cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98287" />
        <display value="Histiocytic and dendritic cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98288" />
        <display value="Macrophage or histiocytic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98289" />
        <display value="Dendritic cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:98290" />
        <display value="Immunodeficiency-associated lymphoproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:98291" />
        <display value="Lymphoproliferative disease associated with primary immune disease" />
      </concept>
      <concept>
        <code value="ORPHA:98292" />
        <display value="Mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:98293" />
        <display value="Hodgkin lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:983" />
        <display value="Testicular regression syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98300" />
        <display value="Idiopathic interstitial pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:98305" />
        <display value="Genetic lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98306" />
        <display value="Familial partial lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98307" />
        <display value="Acquired lipodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98313" />
        <display value="Male infertility due to gonadal dysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:98343" />
        <display value="Male infertility due to obstructive azoospermia" />
      </concept>
      <concept>
        <code value="ORPHA:98345" />
        <display value="Rare idiopathic male infertility" />
      </concept>
      <concept>
        <code value="ORPHA:98349" />
        <display value="Autosomal dominant isolated diffuse palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:98352" />
        <display value="Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:98353" />
        <display value="Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:98356" />
        <display value="Autosomal recessive isolated diffuse palmoplantar keratoderma" />
      </concept>
      <concept>
        <code value="ORPHA:98357" />
        <display value="Autosomal recessive disease with focal palmoplantar keratoderma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:98360" />
        <display value="Constitutional anemia due to iron metabolism disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98362" />
        <display value="Constitutional sideroblastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:98363" />
        <display value="Rare hemolytic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:98364" />
        <display value="Rare constitutional hemolytic anemia due to a red cell membrane anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98365" />
        <display value="Hereditary stomatocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:98366" />
        <display value="Constitutional hemolytic anemia due to acanthocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:98369" />
        <display value="Rare constitutional hemolytic anemia due to an enzyme disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98370" />
        <display value="Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:98372" />
        <display value="Hemolytic anemia due to a disorder of glycolytic enzymes" />
      </concept>
      <concept>
        <code value="ORPHA:98374" />
        <display value="Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98375" />
        <display value="Autoimmune hemolytic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:98396" />
        <display value="Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder" />
      </concept>
      <concept>
        <code value="ORPHA:984" />
        <display value="Pulmonary agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:98408" />
        <display value="Constitutional megaloblastic anemia due to folate metabolism disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98415" />
        <display value="Vitamin B12- and folate-independent constitutional megaloblastic anemia" />
      </concept>
      <concept>
        <code value="ORPHA:98421" />
        <display value="Red cell aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:98427" />
        <display value="Polycythemia" />
      </concept>
      <concept>
        <code value="ORPHA:98428" />
        <display value="Secondary polycythemia" />
      </concept>
      <concept>
        <code value="ORPHA:98429" />
        <display value="Rare coagulation disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98434" />
        <display value="Hereditary combined deficiency of vitamin K-dependent clotting factors" />
      </concept>
      <concept>
        <code value="ORPHA:98455" />
        <display value="Alpha granule disease" />
      </concept>
      <concept>
        <code value="ORPHA:98456" />
        <display value="Dense granule disease" />
      </concept>
      <concept>
        <code value="ORPHA:98464" />
        <display value="X-linked syndromic intellectual disability" />
      </concept>
      <concept>
        <code value="ORPHA:98472" />
        <display value="Skeletal muscle disease" />
      </concept>
      <concept>
        <code value="ORPHA:98473" />
        <display value="Muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98482" />
        <display value="Idiopathic inflammatory myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:98486" />
        <display value="Metabolic myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:98491" />
        <display value="Neuromuscular junction disease" />
      </concept>
      <concept>
        <code value="ORPHA:98494" />
        <display value="Acquired neuromuscular junction disease" />
      </concept>
      <concept>
        <code value="ORPHA:98495" />
        <display value="Genetic neuromuscular junction disease" />
      </concept>
      <concept>
        <code value="ORPHA:98496" />
        <display value="Rare peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:98497" />
        <display value="Genetic peripheral neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:98503" />
        <display value="Motor neuron disease" />
      </concept>
      <concept>
        <code value="ORPHA:98505" />
        <display value="Genetic motor neuron disease" />
      </concept>
      <concept>
        <code value="ORPHA:98506" />
        <display value="Acquired motor neuron disease" />
      </concept>
      <concept>
        <code value="ORPHA:98514" />
        <display value="Malformation of the cerebellar vermis" />
      </concept>
      <concept>
        <code value="ORPHA:98516" />
        <display value="Malformation of the cerebellar hemispheres" />
      </concept>
      <concept>
        <code value="ORPHA:98518" />
        <display value="Cranial nerve and nuclear aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:98519" />
        <display value="Posterior fossa malformation" />
      </concept>
      <concept>
        <code value="ORPHA:98520" />
        <display value="Cystic malformation of the posterior fossa" />
      </concept>
      <concept>
        <code value="ORPHA:98523" />
        <display value="Non-syndromic pontocerebellar hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:98534" />
        <display value="Neurodegenerative disease with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98535" />
        <display value="Frontotemporal degeneration with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98538" />
        <display value="Ataxia with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98539" />
        <display value="Early-onset ataxia with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98540" />
        <display value="Late-onset ataxia with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98542" />
        <display value="Infectious disease with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98543" />
        <display value="Metabolic disease with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98544" />
        <display value="Cerebral lipidosis with dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98549" />
        <display value="Rare cerebrovascular dementia" />
      </concept>
      <concept>
        <code value="ORPHA:98553" />
        <display value="Developmental defect of the eye" />
      </concept>
      <concept>
        <code value="ORPHA:98555" />
        <display value="Microphthalmia-anophthalmia-coloboma" />
      </concept>
      <concept>
        <code value="ORPHA:98557" />
        <display value="Syndromic aniridia" />
      </concept>
      <concept>
        <code value="ORPHA:98560" />
        <display value="Rare palpebral disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98561" />
        <display value="Congenital malformation of the eyelid" />
      </concept>
      <concept>
        <code value="ORPHA:98562" />
        <display value="Cryptophthalmia" />
      </concept>
      <concept>
        <code value="ORPHA:98563" />
        <display value="Microblepharon-ablephara syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98564" />
        <display value="Eyelid border anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98565" />
        <display value="Syndromic ankyloblepharon filiforme adnatum" />
      </concept>
      <concept>
        <code value="ORPHA:98566" />
        <display value="Syndromic eyelid coloboma" />
      </concept>
      <concept>
        <code value="ORPHA:98567" />
        <display value="Rare eyelid malposition disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98570" />
        <display value="Congenital ectropion" />
      </concept>
      <concept>
        <code value="ORPHA:98571" />
        <display value="Secondary ectropion" />
      </concept>
      <concept>
        <code value="ORPHA:98574" />
        <display value="Syndromic epicanthus" />
      </concept>
      <concept>
        <code value="ORPHA:98575" />
        <display value="Syndromic telecanthus" />
      </concept>
      <concept>
        <code value="ORPHA:98576" />
        <display value="Syndromic outer canthal malposition" />
      </concept>
      <concept>
        <code value="ORPHA:98578" />
        <display value="Rare disorder with ptosis" />
      </concept>
      <concept>
        <code value="ORPHA:98594" />
        <display value="Rare eyebrow/eyelash disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98602" />
        <display value="Rare disorder of the lacrimal apparatus" />
      </concept>
      <concept>
        <code value="ORPHA:98604" />
        <display value="Congenital alacrima" />
      </concept>
      <concept>
        <code value="ORPHA:98605" />
        <display value="Lacrimal drainage system anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98606" />
        <display value="Syndromic orbital border hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:98609" />
        <display value="EEC syndrome and related disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98610" />
        <display value="Rare disorder with conjunctival involvement as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:98618" />
        <display value="Rare refraction anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98619" />
        <display value="Rare isolated myopia" />
      </concept>
      <concept>
        <code value="ORPHA:98621" />
        <display value="Rare hyperopia and astigmatism" />
      </concept>
      <concept>
        <code value="ORPHA:98622" />
        <display value="Syndromic hyperopia" />
      </concept>
      <concept>
        <code value="ORPHA:98623" />
        <display value="Syndromic keratoconus" />
      </concept>
      <concept>
        <code value="ORPHA:98625" />
        <display value="Superficial corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98626" />
        <display value="Stromal corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98627" />
        <display value="Posterior corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98628" />
        <display value="Syndromic corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98631" />
        <display value="Congenital malformation of the eye with glaucoma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:98634" />
        <display value="Anterior segment developmental anomaly without extraocular manifestation" />
      </concept>
      <concept>
        <code value="ORPHA:98635" />
        <display value="Corneodysgenesis" />
      </concept>
      <concept>
        <code value="ORPHA:98638" />
        <display value="Rare disease with glaucoma as a major feature" />
      </concept>
      <concept>
        <code value="ORPHA:98639" />
        <display value="Rare lens disease" />
      </concept>
      <concept>
        <code value="ORPHA:98640" />
        <display value="Rare disorder with lens opacification" />
      </concept>
      <concept>
        <code value="ORPHA:98641" />
        <display value="Syndromic cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98642" />
        <display value="Chromosomal anomaly with cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98644" />
        <display value="Metabolic disease with cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98646" />
        <display value="Renal disease with cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98648" />
        <display value="Musculoskeletal disease with cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98649" />
        <display value="Dentocutaneous disease with cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98650" />
        <display value="Craniofacial anomaly with cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98652" />
        <display value="Lens size anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98653" />
        <display value="Lens position anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98655" />
        <display value="Lens shape anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98658" />
        <display value="Color-vision disease" />
      </concept>
      <concept>
        <code value="ORPHA:98661" />
        <display value="Syndromic rod-cone dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98668" />
        <display value="Vitreoretinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:98671" />
        <display value="Hereditary optic neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:98672" />
        <display value="Autosomal dominant optic atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98673" />
        <display value="Autosomal dominant optic atrophy, classic form" />
      </concept>
      <concept>
        <code value="ORPHA:98676" />
        <display value="Autosomal recessive isolated optic atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98681" />
        <display value="Rare disorder with strabismus" />
      </concept>
      <concept>
        <code value="ORPHA:98683" />
        <display value="Syndromic disorder with strabismus" />
      </concept>
      <concept>
        <code value="ORPHA:98684" />
        <display value="Craniostenosis with strabismus" />
      </concept>
      <concept>
        <code value="ORPHA:98685" />
        <display value="Rare oculomotor nerve disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98686" />
        <display value="Congenital trochlear nerve palsy" />
      </concept>
      <concept>
        <code value="ORPHA:98687" />
        <display value="Supranuclear eye movement disorder" />
      </concept>
      <concept>
        <code value="ORPHA:98688" />
        <display value="Oculomotor apraxia" />
      </concept>
      <concept>
        <code value="ORPHA:98706" />
        <display value="Oculocutaneous or ocular albinism" />
      </concept>
      <concept>
        <code value="ORPHA:98715" />
        <display value="Uveitis" />
      </concept>
      <concept>
        <code value="ORPHA:98716" />
        <display value="Heart position anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98717" />
        <display value="Transposition of the great arteries and conotruncal cardiac anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98718" />
        <display value="Aortic malformation" />
      </concept>
      <concept>
        <code value="ORPHA:98719" />
        <display value="Pulmonary artery or pulmonary branch anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98720" />
        <display value="Atrioventricular valve anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98721" />
        <display value="Congenital tricuspid malformation" />
      </concept>
      <concept>
        <code value="ORPHA:98722" />
        <display value="Atrioventricular canal defect" />
      </concept>
      <concept>
        <code value="ORPHA:98723" />
        <display value="Hypoplastic right heart syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98724" />
        <display value="Congenital anomaly of the great arteries" />
      </concept>
      <concept>
        <code value="ORPHA:98725" />
        <display value="Ascending aorta anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98727" />
        <display value="Rare atrial defect and interatrial communication" />
      </concept>
      <concept>
        <code value="ORPHA:98729" />
        <display value="Congenital pulmonary veins anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98731" />
        <display value="Congenital arteriovenous fistula" />
      </concept>
      <concept>
        <code value="ORPHA:98733" />
        <display value="Noonan syndrome and Noonan-related syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98754" />
        <display value="Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15" />
      </concept>
      <concept>
        <code value="ORPHA:98755" />
        <display value="Spinocerebellar ataxia type 1" />
      </concept>
      <concept>
        <code value="ORPHA:98756" />
        <display value="Spinocerebellar ataxia type 2" />
      </concept>
      <concept>
        <code value="ORPHA:98757" />
        <display value="Spinocerebellar ataxia type 3" />
      </concept>
      <concept>
        <code value="ORPHA:98758" />
        <display value="Spinocerebellar ataxia type 6" />
      </concept>
      <concept>
        <code value="ORPHA:98759" />
        <display value="Spinocerebellar ataxia type 17" />
      </concept>
      <concept>
        <code value="ORPHA:98760" />
        <display value="Spinocerebellar ataxia type 8" />
      </concept>
      <concept>
        <code value="ORPHA:98761" />
        <display value="Spinocerebellar ataxia type 10" />
      </concept>
      <concept>
        <code value="ORPHA:98762" />
        <display value="Spinocerebellar ataxia type 12" />
      </concept>
      <concept>
        <code value="ORPHA:98763" />
        <display value="Spinocerebellar ataxia type 14" />
      </concept>
      <concept>
        <code value="ORPHA:98764" />
        <display value="Spinocerebellar ataxia type 27" />
      </concept>
      <concept>
        <code value="ORPHA:98765" />
        <display value="Spinocerebellar ataxia type 4" />
      </concept>
      <concept>
        <code value="ORPHA:98766" />
        <display value="Spinocerebellar ataxia type 5" />
      </concept>
      <concept>
        <code value="ORPHA:98767" />
        <display value="Spinocerebellar ataxia type 11" />
      </concept>
      <concept>
        <code value="ORPHA:98768" />
        <display value="Spinocerebellar ataxia type 13" />
      </concept>
      <concept>
        <code value="ORPHA:98769" />
        <display value="Spinocerebellar ataxia type 15/16" />
      </concept>
      <concept>
        <code value="ORPHA:98771" />
        <display value="Spinocerebellar ataxia type 18" />
      </concept>
      <concept>
        <code value="ORPHA:98772" />
        <display value="Spinocerebellar ataxia type 19/22" />
      </concept>
      <concept>
        <code value="ORPHA:98773" />
        <display value="Spinocerebellar ataxia type 21" />
      </concept>
      <concept>
        <code value="ORPHA:98784" />
        <display value="Autosomal dominant nocturnal frontal lobe epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:98791" />
        <display value="Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16" />
      </concept>
      <concept>
        <code value="ORPHA:98793" />
        <display value="Prader-Willi syndrome due to paternal 15q11q13 deletion" />
      </concept>
      <concept>
        <code value="ORPHA:98794" />
        <display value="Angelman syndrome due to maternal 15q11q13 deletion" />
      </concept>
      <concept>
        <code value="ORPHA:98795" />
        <display value="Angelman syndrome due to paternal uniparental disomy of chromosome 15" />
      </concept>
      <concept>
        <code value="ORPHA:98797" />
        <display value="Isochromosomy Yp" />
      </concept>
      <concept>
        <code value="ORPHA:98798" />
        <display value="Isochromosomy Yq" />
      </concept>
      <concept>
        <code value="ORPHA:988" />
        <display value="Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98805" />
        <display value="Primary dystonia, DYT4 type" />
      </concept>
      <concept>
        <code value="ORPHA:98806" />
        <display value="Primary dystonia, DYT6 type" />
      </concept>
      <concept>
        <code value="ORPHA:98807" />
        <display value="Primary dystonia, DYT13 type" />
      </concept>
      <concept>
        <code value="ORPHA:98808" />
        <display value="Autosomal dominant dopa-responsive dystonia" />
      </concept>
      <concept>
        <code value="ORPHA:98809" />
        <display value="Paroxysmal kinesigenic dyskinesia" />
      </concept>
      <concept>
        <code value="ORPHA:98810" />
        <display value="Paroxysmal non-kinesigenic dyskinesia" />
      </concept>
      <concept>
        <code value="ORPHA:98811" />
        <display value="Paroxysmal exertion-induced dyskinesia" />
      </concept>
      <concept>
        <code value="ORPHA:98813" />
        <display value="Hypohidrotic ectodermal dysplasia with immunodeficiency" />
      </concept>
      <concept>
        <code value="ORPHA:98815" />
        <display value="Benign childhood occipital epilepsy, Panayiotopoulos type" />
      </concept>
      <concept>
        <code value="ORPHA:98816" />
        <display value="Benign childhood occipital epilepsy, Gastaut type" />
      </concept>
      <concept>
        <code value="ORPHA:98818" />
        <display value="Landau-Kleffner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98819" />
        <display value="Familial temporal lobe epilepsy" />
      </concept>
      <concept>
        <code value="ORPHA:98820" />
        <display value="Familial focal epilepsy with variable foci" />
      </concept>
      <concept>
        <code value="ORPHA:98823" />
        <display value="Chronic myelomonocytic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:98824" />
        <display value="Atypical chronic myeloid leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:98825" />
        <display value="Unclassified myelodysplastic/myeloproliferative disease" />
      </concept>
      <concept>
        <code value="ORPHA:98826" />
        <display value="Refractory anemia" />
      </concept>
      <concept>
        <code value="ORPHA:98827" />
        <display value="Unclassified myelodysplastic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98829" />
        <display value="Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)" />
      </concept>
      <concept>
        <code value="ORPHA:98831" />
        <display value="Acute myeloid leukemia with 11q23 abnormalities" />
      </concept>
      <concept>
        <code value="ORPHA:98832" />
        <display value="Acute myeloid leukemia with minimal differentiation" />
      </concept>
      <concept>
        <code value="ORPHA:98833" />
        <display value="Acute myeloblastic leukemia without maturation" />
      </concept>
      <concept>
        <code value="ORPHA:98834" />
        <display value="Acute myeloblastic leukemia with maturation" />
      </concept>
      <concept>
        <code value="ORPHA:98835" />
        <display value="Acute undifferentiated leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:98836" />
        <display value="Bilineal acute leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:98837" />
        <display value="Acute biphenotypic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:98838" />
        <display value="Primary mediastinal large B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:98839" />
        <display value="Intravascular large B-cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:98841" />
        <display value="Anaplastic large cell lymphoma" />
      </concept>
      <concept>
        <code value="ORPHA:98842" />
        <display value="Lymphomatoid papulosis" />
      </concept>
      <concept>
        <code value="ORPHA:98843" />
        <display value="Classic Hodgkin lymphoma, nodular sclerosis type" />
      </concept>
      <concept>
        <code value="ORPHA:98844" />
        <display value="Classic Hodgkin lymphoma, mixed cellularity type" />
      </concept>
      <concept>
        <code value="ORPHA:98845" />
        <display value="Classic Hodgkin lymphoma, lymphocyte-rich type" />
      </concept>
      <concept>
        <code value="ORPHA:98846" />
        <display value="Classic Hodgkin lymphoma, lymphocyte-depleted type" />
      </concept>
      <concept>
        <code value="ORPHA:98848" />
        <display value="Indolent systemic mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:98849" />
        <display value="Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease" />
      </concept>
      <concept>
        <code value="ORPHA:98850" />
        <display value="Aggressive systemic mastocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:98851" />
        <display value="Mast cell leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:98852" />
        <display value="Desquamative interstitial pneumonia" />
      </concept>
      <concept>
        <code value="ORPHA:98853" />
        <display value="Autosomal dominant Emery-Dreifuss muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98855" />
        <display value="Autosomal recessive Emery-Dreifuss muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98856" />
        <display value="Charcot-Marie-Tooth disease type 2B1" />
      </concept>
      <concept>
        <code value="ORPHA:98863" />
        <display value="X-linked Emery-Dreifuss muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98868" />
        <display value="Southeast Asian ovalocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:98869" />
        <display value="Congenital dyserythropoietic anemia type I" />
      </concept>
      <concept>
        <code value="ORPHA:98870" />
        <display value="Congenital dyserythropoietic anemia type III" />
      </concept>
      <concept>
        <code value="ORPHA:98871" />
        <display value="Transient erythroblastopenia of childhood" />
      </concept>
      <concept>
        <code value="ORPHA:98872" />
        <display value="Adult pure red cell aplasia" />
      </concept>
      <concept>
        <code value="ORPHA:98873" />
        <display value="Congenital dyserythropoietic anemia type II" />
      </concept>
      <concept>
        <code value="ORPHA:98878" />
        <display value="Hemophilia A" />
      </concept>
      <concept>
        <code value="ORPHA:98879" />
        <display value="Hemophilia B" />
      </concept>
      <concept>
        <code value="ORPHA:98880" />
        <display value="Familial afibrinogenemia" />
      </concept>
      <concept>
        <code value="ORPHA:98881" />
        <display value="Familial dysfibrinogenemia" />
      </concept>
      <concept>
        <code value="ORPHA:98885" />
        <display value="Bleeding diathesis due to glycoprotein VI deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:98886" />
        <display value="Bleeding diathesis due to integrin alpha2-beta1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:98888" />
        <display value="X-linked complex spastic paraplegia" />
      </concept>
      <concept>
        <code value="ORPHA:98889" />
        <display value="Bilateral perisylvian polymicrogyria" />
      </concept>
      <concept>
        <code value="ORPHA:98890" />
        <display value="Early-onset X-linked optic atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98892" />
        <display value="Periventricular nodular heterotopia" />
      </concept>
      <concept>
        <code value="ORPHA:98893" />
        <display value="Congenital muscular dystrophy type 1B" />
      </concept>
      <concept>
        <code value="ORPHA:98895" />
        <display value="Becker muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98896" />
        <display value="Duchenne muscular dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98897" />
        <display value="Oculopharyngodistal myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:989" />
        <display value="Hypoglossia-hypodactyly syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98902" />
        <display value="Amish nemaline myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:98904" />
        <display value="Congenital myopathy with excess of thin filaments" />
      </concept>
      <concept>
        <code value="ORPHA:98905" />
        <display value="Congenital multicore myopathy with external ophthalmoplegia" />
      </concept>
      <concept>
        <code value="ORPHA:98907" />
        <display value="Dorfman-Chanarin disease" />
      </concept>
      <concept>
        <code value="ORPHA:98908" />
        <display value="Neutral lipid storage myopathy" />
      </concept>
      <concept>
        <code value="ORPHA:98909" />
        <display value="Desminopathy" />
      </concept>
      <concept>
        <code value="ORPHA:98910" />
        <display value="Alpha-crystallinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:98911" />
        <display value="Distal myotilinopathy" />
      </concept>
      <concept>
        <code value="ORPHA:98912" />
        <display value="Late-onset distal myopathy, Markesbery-Griggs type" />
      </concept>
      <concept>
        <code value="ORPHA:98913" />
        <display value="Postsynaptic congenital myasthenic syndromes" />
      </concept>
      <concept>
        <code value="ORPHA:98914" />
        <display value="Presynaptic congenital myasthenic syndromes" />
      </concept>
      <concept>
        <code value="ORPHA:98915" />
        <display value="Synaptic congenital myasthenic syndromes" />
      </concept>
      <concept>
        <code value="ORPHA:98916" />
        <display value="Acute inflammatory demyelinating polyradiculoneuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:98917" />
        <display value="Acute motor and sensory axonal neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:98918" />
        <display value="Acute motor axonal neuropathy" />
      </concept>
      <concept>
        <code value="ORPHA:98919" />
        <display value="Miller-Fisher syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98920" />
        <display value="Spinal muscular atrophy with respiratory distress type 1" />
      </concept>
      <concept>
        <code value="ORPHA:98922" />
        <display value="Blake pouch cyst" />
      </concept>
      <concept>
        <code value="ORPHA:98933" />
        <display value="Multiple system atrophy, parkinsonian type" />
      </concept>
      <concept>
        <code value="ORPHA:98934" />
        <display value="Huntington disease-like 2" />
      </concept>
      <concept>
        <code value="ORPHA:98938" />
        <display value="Colobomatous microphthalmia" />
      </concept>
      <concept>
        <code value="ORPHA:98942" />
        <display value="Coloboma of choroid and retina" />
      </concept>
      <concept>
        <code value="ORPHA:98943" />
        <display value="Coloboma of eye lens" />
      </concept>
      <concept>
        <code value="ORPHA:98944" />
        <display value="Coloboma of iris" />
      </concept>
      <concept>
        <code value="ORPHA:98945" />
        <display value="Coloboma of macula" />
      </concept>
      <concept>
        <code value="ORPHA:98946" />
        <display value="Coloboma of eyelid" />
      </concept>
      <concept>
        <code value="ORPHA:98947" />
        <display value="Coloboma of optic disc" />
      </concept>
      <concept>
        <code value="ORPHA:98948" />
        <display value="Congenital symblepharon" />
      </concept>
      <concept>
        <code value="ORPHA:98949" />
        <display value="Complete cryptophthalmia" />
      </concept>
      <concept>
        <code value="ORPHA:98950" />
        <display value="Partial cryptophthalmia" />
      </concept>
      <concept>
        <code value="ORPHA:98951" />
        <display value="Inverse Marcus-Gunn phenomenon" />
      </concept>
      <concept>
        <code value="ORPHA:98954" />
        <display value="Meesmann corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98955" />
        <display value="Lisch epithelial corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98956" />
        <display value="Epithelial basement membrane dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98957" />
        <display value="Gelatinous drop-like corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98958" />
        <display value="Honey-droplet corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98959" />
        <display value="Subepithelial mucinous corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98960" />
        <display value="Thiel-Behnke corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98961" />
        <display value="Reis-Bucklers corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98962" />
        <display value="Granular corneal dystrophy type I" />
      </concept>
      <concept>
        <code value="ORPHA:98963" />
        <display value="Granular corneal dystrophy type II" />
      </concept>
      <concept>
        <code value="ORPHA:98964" />
        <display value="Lattice corneal dystrophy type I" />
      </concept>
      <concept>
        <code value="ORPHA:98967" />
        <display value="Schnyder corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98969" />
        <display value="Macular corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98970" />
        <display value="Fleck corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98971" />
        <display value="Posterior amorphous corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98972" />
        <display value="Central cloudy dystrophy of Francois" />
      </concept>
      <concept>
        <code value="ORPHA:98973" />
        <display value="Posterior polymorphous corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98974" />
        <display value="Fuchs endothelial corneal dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98975" />
        <display value="Congenital hereditary endothelial dystrophy type I" />
      </concept>
      <concept>
        <code value="ORPHA:98976" />
        <display value="Congenital glaucoma" />
      </concept>
      <concept>
        <code value="ORPHA:98977" />
        <display value="Juvenile glaucoma" />
      </concept>
      <concept>
        <code value="ORPHA:98978" />
        <display value="Axenfeld anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:98979" />
        <display value="Chandler syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98980" />
        <display value="Cogan-Reese syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:98981" />
        <display value="Essential iris atrophy" />
      </concept>
      <concept>
        <code value="ORPHA:98984" />
        <display value="Pulverulent cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98985" />
        <display value="Early-onset sutural cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98988" />
        <display value="Early-onset anterior polar cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98989" />
        <display value="Cerulean cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98990" />
        <display value="Coralliform cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98991" />
        <display value="Early-onset nuclear cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98992" />
        <display value="Early-onset partial cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98993" />
        <display value="Early-onset posterior polar cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98994" />
        <display value="Total early-onset cataract" />
      </concept>
      <concept>
        <code value="ORPHA:98995" />
        <display value="Early-onset zonular cataract" />
      </concept>
      <concept>
        <code value="ORPHA:99" />
        <display value="Autosomal dominant cerebellar ataxia" />
      </concept>
      <concept>
        <code value="ORPHA:990" />
        <display value="Agnathia-holoprosencephaly-situs inversus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99000" />
        <display value="Adult-onset foveomacular vitelliform dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:99001" />
        <display value="Butterfly-shaped pigment dystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:99002" />
        <display value="Reticular dystrophy of the retinal pigment epithelium" />
      </concept>
      <concept>
        <code value="ORPHA:99003" />
        <display value="Multifocal pattern dystrophy simulating fundus flavimaculatus" />
      </concept>
      <concept>
        <code value="ORPHA:99004" />
        <display value="Fundus pulverulentus" />
      </concept>
      <concept>
        <code value="ORPHA:99013" />
        <display value="Spastic paraplegia type 7" />
      </concept>
      <concept>
        <code value="ORPHA:99014" />
        <display value="X-linked Charcot-Marie-Tooth disease type 5" />
      </concept>
      <concept>
        <code value="ORPHA:99015" />
        <display value="Spastic paraplegia type 2" />
      </concept>
      <concept>
        <code value="ORPHA:99022" />
        <display value="Niemann-Pick disease type E" />
      </concept>
      <concept>
        <code value="ORPHA:99027" />
        <display value="Adult-onset autosomal dominant leukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:99042" />
        <display value="Congenitally uncorrected transposition of the great arteries with coarctation" />
      </concept>
      <concept>
        <code value="ORPHA:99043" />
        <display value="Double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:99045" />
        <display value="Double outlet right ventricle with subpulmonary ventricular septal defect" />
      </concept>
      <concept>
        <code value="ORPHA:99046" />
        <display value="Double outlet right ventricle with non-committed subpulmonary ventricular septal defect" />
      </concept>
      <concept>
        <code value="ORPHA:99048" />
        <display value="Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99049" />
        <display value="Pulmonary artery coming from patent ductus arteriosus" />
      </concept>
      <concept>
        <code value="ORPHA:99050" />
        <display value="Pulmonary artery coming from the aorta" />
      </concept>
      <concept>
        <code value="ORPHA:99051" />
        <display value="Discrete fixed membranous subaortic stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:99052" />
        <display value="Discrete fibromuscular subaortic stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:99053" />
        <display value="Tunnel subaortic stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:99054" />
        <display value="Valvular pulmonary stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:99055" />
        <display value="Congenital anomaly of the tricuspid valve chordae" />
      </concept>
      <concept>
        <code value="ORPHA:99056" />
        <display value="Parachute tricuspid valve" />
      </concept>
      <concept>
        <code value="ORPHA:99057" />
        <display value="Congenital mitral stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:99058" />
        <display value="Hypoplasia of the mitral valve annulus" />
      </concept>
      <concept>
        <code value="ORPHA:99059" />
        <display value="Congenital supravalvular mitral ring" />
      </concept>
      <concept>
        <code value="ORPHA:99060" />
        <display value="Congenital unguarded mitral orifice" />
      </concept>
      <concept>
        <code value="ORPHA:99061" />
        <display value="Accessory mitral valve tissue" />
      </concept>
      <concept>
        <code value="ORPHA:99062" />
        <display value="Mitral valve agenesis" />
      </concept>
      <concept>
        <code value="ORPHA:99063" />
        <display value="Shone complex" />
      </concept>
      <concept>
        <code value="ORPHA:99064" />
        <display value="Straddling and/or overriding mitral valve" />
      </concept>
      <concept>
        <code value="ORPHA:99066" />
        <display value="Complete atrioventricular canal-left heart obstruction syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99067" />
        <display value="Complete atrioventricular canal-ventricle hypoplasia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99068" />
        <display value="Complete atrioventricular canal-tetralogy of Fallot syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99069" />
        <display value="Univentricular heart with single atrio-ventricular valve" />
      </concept>
      <concept>
        <code value="ORPHA:99070" />
        <display value="Aorto-right ventricular tunnel" />
      </concept>
      <concept>
        <code value="ORPHA:99071" />
        <display value="Aorto-left ventricular tunnel" />
      </concept>
      <concept>
        <code value="ORPHA:99072" />
        <display value="Congenital patent ductus arteriosus aneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:99075" />
        <display value="Encircling double aortic arch" />
      </concept>
      <concept>
        <code value="ORPHA:99076" />
        <display value="Persistent fifth aortic arch" />
      </concept>
      <concept>
        <code value="ORPHA:99077" />
        <display value="Kommerell diverticulum" />
      </concept>
      <concept>
        <code value="ORPHA:99078" />
        <display value="Neuhauser anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:99079" />
        <display value="Cervical aortic arch" />
      </concept>
      <concept>
        <code value="ORPHA:99081" />
        <display value="Right aortic arch" />
      </concept>
      <concept>
        <code value="ORPHA:99082" />
        <display value="Dysphagia lusoria" />
      </concept>
      <concept>
        <code value="ORPHA:99083" />
        <display value="Pulmonary artery hypoplasia" />
      </concept>
      <concept>
        <code value="ORPHA:99084" />
        <display value="Peripheral pulmonary stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:99085" />
        <display value="Coronary artery intramyocardial course" />
      </concept>
      <concept>
        <code value="ORPHA:99086" />
        <display value="Aortopulmonary coronary arterial course" />
      </concept>
      <concept>
        <code value="ORPHA:99087" />
        <display value="Congenital stenosis or atresia of the coronary ostium" />
      </concept>
      <concept>
        <code value="ORPHA:99088" />
        <display value="Intramural coronary arterial course" />
      </concept>
      <concept>
        <code value="ORPHA:99089" />
        <display value="Abnormal number of coronary ostia" />
      </concept>
      <concept>
        <code value="ORPHA:99090" />
        <display value="Malposition of the coronary ostium" />
      </concept>
      <concept>
        <code value="ORPHA:99092" />
        <display value="Interventricular septum aneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:99094" />
        <display value="Laubry-Pezzi syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99095" />
        <display value="Congenital Gerbode defect" />
      </concept>
      <concept>
        <code value="ORPHA:99098" />
        <display value="Cor triatriatum dexter" />
      </concept>
      <concept>
        <code value="ORPHA:99099" />
        <display value="Cor triatriatum sinister" />
      </concept>
      <concept>
        <code value="ORPHA:991" />
        <display value="PAGOD syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99100" />
        <display value="Juxtaposition of the atrial appendages" />
      </concept>
      <concept>
        <code value="ORPHA:99101" />
        <display value="Ectasia of the right atrial appendage" />
      </concept>
      <concept>
        <code value="ORPHA:99102" />
        <display value="Ectasia of the left atrial appendage" />
      </concept>
      <concept>
        <code value="ORPHA:99103" />
        <display value="Atrial septal defect, ostium secundum type" />
      </concept>
      <concept>
        <code value="ORPHA:99104" />
        <display value="Atrial septal defect, coronary sinus type" />
      </concept>
      <concept>
        <code value="ORPHA:99105" />
        <display value="Atrial septal defect, sinus venosus type" />
      </concept>
      <concept>
        <code value="ORPHA:99106" />
        <display value="Atrial septal defect, ostium primum type" />
      </concept>
      <concept>
        <code value="ORPHA:99107" />
        <display value="Atrial septal aneurysm" />
      </concept>
      <concept>
        <code value="ORPHA:99109" />
        <display value="Persistent left superior vena cava connecting to the left-sided atrium" />
      </concept>
      <concept>
        <code value="ORPHA:99110" />
        <display value="Right superior vena cava connecting to left-sided atrium" />
      </concept>
      <concept>
        <code value="ORPHA:99111" />
        <display value="Left superior vena cava persisting to left-sided atrium" />
      </concept>
      <concept>
        <code value="ORPHA:99112" />
        <display value="Absence of innominate vein" />
      </concept>
      <concept>
        <code value="ORPHA:99113" />
        <display value="Subaortic course of innominate vein" />
      </concept>
      <concept>
        <code value="ORPHA:99114" />
        <display value="Agenesis of the superior vena cava" />
      </concept>
      <concept>
        <code value="ORPHA:99117" />
        <display value="Coronary sinus stenosis" />
      </concept>
      <concept>
        <code value="ORPHA:99118" />
        <display value="Coronary sinus atresia" />
      </concept>
      <concept>
        <code value="ORPHA:99119" />
        <display value="Right inferior vena cava connecting to left-sided atrium" />
      </concept>
      <concept>
        <code value="ORPHA:99120" />
        <display value="Persistent eustachian valve" />
      </concept>
      <concept>
        <code value="ORPHA:99121" />
        <display value="Azygos continuation of the inferior vena cava" />
      </concept>
      <concept>
        <code value="ORPHA:99122" />
        <display value="Congenital stenosis of the inferior vena cava" />
      </concept>
      <concept>
        <code value="ORPHA:99123" />
        <display value="Inferior vena cava interruption" />
      </concept>
      <concept>
        <code value="ORPHA:99124" />
        <display value="Congenital partial pulmonary venous return anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:99125" />
        <display value="Congenital total pulmonary venous return anomaly" />
      </concept>
      <concept>
        <code value="ORPHA:99129" />
        <display value="Congenital complete agenesis of pericardium" />
      </concept>
      <concept>
        <code value="ORPHA:99130" />
        <display value="Congenital partial agenesis of pericardium" />
      </concept>
      <concept>
        <code value="ORPHA:99131" />
        <display value="Pleuro-pericardial cyst" />
      </concept>
      <concept>
        <code value="ORPHA:99135" />
        <display value="6-phosphogluconate dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:99138" />
        <display value="Hemolytic anemia due to erythrocyte adenosine deaminase overproduction" />
      </concept>
      <concept>
        <code value="ORPHA:99139" />
        <display value="Unstable hemoglobin disease" />
      </concept>
      <concept>
        <code value="ORPHA:99141" />
        <display value="Lymphedema-posterior choanal atresia syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99147" />
        <display value="Acquired von Willebrand syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99169" />
        <display value="Epiblepharon" />
      </concept>
      <concept>
        <code value="ORPHA:99170" />
        <display value="Tarsal kink syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99171" />
        <display value="Isolated congenital ectropion" />
      </concept>
      <concept>
        <code value="ORPHA:99172" />
        <display value="Euryblepharon" />
      </concept>
      <concept>
        <code value="ORPHA:99176" />
        <display value="Congenital eyelid retraction" />
      </concept>
      <concept>
        <code value="ORPHA:99177" />
        <display value="Isolated distichiasis" />
      </concept>
      <concept>
        <code value="ORPHA:99179" />
        <display value="Kandori fleck retina" />
      </concept>
      <concept>
        <code value="ORPHA:99226" />
        <display value="Monosomy X" />
      </concept>
      <concept>
        <code value="ORPHA:99228" />
        <display value="Mosaic monosomy X" />
      </concept>
      <concept>
        <code value="ORPHA:99324" />
        <display value="Paternal uniparental disomy of chromosome 13" />
      </concept>
      <concept>
        <code value="ORPHA:99329" />
        <display value="48,XYYY syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99330" />
        <display value="49,XYYYY syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99361" />
        <display value="Familial medullary thyroid carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:994" />
        <display value="Fetal akinesia deformation sequence" />
      </concept>
      <concept>
        <code value="ORPHA:99408" />
        <display value="Pituitary adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:99413" />
        <display value="Turner syndrome due to structural X chromosome anomalies" />
      </concept>
      <concept>
        <code value="ORPHA:99429" />
        <display value="Complete androgen insensitivity syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99642" />
        <display value="Spondyloepimetaphyseal dysplasia, Handigodu type" />
      </concept>
      <concept>
        <code value="ORPHA:99646" />
        <display value="Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria" />
      </concept>
      <concept>
        <code value="ORPHA:99647" />
        <display value="Cheirospondyloenchondromatosis" />
      </concept>
      <concept>
        <code value="ORPHA:99657" />
        <display value="Primary dystonia, DYT2 type" />
      </concept>
      <concept>
        <code value="ORPHA:99672" />
        <display value="Frieds tooth and nail syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99688" />
        <display value="Dermotrichic syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99701" />
        <display value="Mesial temporal lobe epilepsy with hippocampal sclerosis" />
      </concept>
      <concept>
        <code value="ORPHA:99718" />
        <display value="Leber plus disease" />
      </concept>
      <concept>
        <code value="ORPHA:99725" />
        <display value="Pituitary gigantism" />
      </concept>
      <concept>
        <code value="ORPHA:99731" />
        <display value="Isolated sulfite oxidase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:99732" />
        <display value="Sulfite oxidase deficiency due to molybdenum cofactor deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:99734" />
        <display value="Myotonia fluctuans" />
      </concept>
      <concept>
        <code value="ORPHA:99735" />
        <display value="Myotonia permanens" />
      </concept>
      <concept>
        <code value="ORPHA:99736" />
        <display value="Acetazolamide-responsive myotonia" />
      </concept>
      <concept>
        <code value="ORPHA:99739" />
        <display value="Rare familial disorder with hypertrophic cardiomyopathy" />
      </concept>
      <concept>
        <code value="ORPHA:99741" />
        <display value="King-Denborough syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99742" />
        <display value="Amish lethal microcephaly" />
      </concept>
      <concept>
        <code value="ORPHA:99745" />
        <display value="Typhoid" />
      </concept>
      <concept>
        <code value="ORPHA:99748" />
        <display value="Pontiac fever" />
      </concept>
      <concept>
        <code value="ORPHA:99749" />
        <display value="Kostmann syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99750" />
        <display value="Atypical progressive supranuclear palsy syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99756" />
        <display value="Alveolar rhabdomyosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:99757" />
        <display value="Embryonal rhabdomyosarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:99763" />
        <display value="Familial hyperreninemic hypoaldosteronism type 1" />
      </concept>
      <concept>
        <code value="ORPHA:99764" />
        <display value="Familial hyperreninemic hypoaldosteronism type 2" />
      </concept>
      <concept>
        <code value="ORPHA:99771" />
        <display value="Bifid uvula" />
      </concept>
      <concept>
        <code value="ORPHA:99772" />
        <display value="Cleft velum" />
      </concept>
      <concept>
        <code value="ORPHA:99776" />
        <display value="Mosaic trisomy 9" />
      </concept>
      <concept>
        <code value="ORPHA:99789" />
        <display value="Dentin dysplasia type I" />
      </concept>
      <concept>
        <code value="ORPHA:99791" />
        <display value="Dentin dysplasia type II" />
      </concept>
      <concept>
        <code value="ORPHA:99792" />
        <display value="Dentin dysplasia-sclerotic bones syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99796" />
        <display value="Subcortical band heterotopia" />
      </concept>
      <concept>
        <code value="ORPHA:99797" />
        <display value="Anodontia" />
      </concept>
      <concept>
        <code value="ORPHA:99798" />
        <display value="Oligodontia" />
      </concept>
      <concept>
        <code value="ORPHA:998" />
        <display value="Albinism-deafness syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99802" />
        <display value="Hemimegalencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:99803" />
        <display value="Haddad syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99806" />
        <display value="Oculootodental syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99807" />
        <display value="PEHO-like syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99810" />
        <display value="Familial porencephaly" />
      </concept>
      <concept>
        <code value="ORPHA:99811" />
        <display value="Neuronal intestinal pseudoobstruction" />
      </concept>
      <concept>
        <code value="ORPHA:99812" />
        <display value="LIG4 syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99818" />
        <display value="Turcot syndrome with polyposis" />
      </concept>
      <concept>
        <code value="ORPHA:99819" />
        <display value="Familial gestational hyperthyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:99824" />
        <display value="Lassa fever" />
      </concept>
      <concept>
        <code value="ORPHA:99825" />
        <display value="Nipah virus disease" />
      </concept>
      <concept>
        <code value="ORPHA:99826" />
        <display value="Marburg hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:99827" />
        <display value="Crimean-Congo hemorrhagic fever" />
      </concept>
      <concept>
        <code value="ORPHA:99828" />
        <display value="Dengue fever" />
      </concept>
      <concept>
        <code value="ORPHA:99829" />
        <display value="Yellow fever" />
      </concept>
      <concept>
        <code value="ORPHA:99832" />
        <display value="Resistance to thyrotropin-releasing hormone syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99842" />
        <display value="Leukocyte adhesion deficiency type I" />
      </concept>
      <concept>
        <code value="ORPHA:99843" />
        <display value="Leukocyte adhesion deficiency type II" />
      </concept>
      <concept>
        <code value="ORPHA:99844" />
        <display value="Leukocyte adhesion deficiency type III" />
      </concept>
      <concept>
        <code value="ORPHA:99845" />
        <display value="Genetic recurrent myoglobinuria" />
      </concept>
      <concept>
        <code value="ORPHA:99846" />
        <display value="Autosomal dominant myoglobinuria" />
      </concept>
      <concept>
        <code value="ORPHA:99849" />
        <display value="Glycogen storage disease due to muscle beta-enolase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:99852" />
        <display value="Ravine syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99853" />
        <display value="Ovarioleukodystrophy" />
      </concept>
      <concept>
        <code value="ORPHA:99854" />
        <display value="Cree leukoencephalopathy" />
      </concept>
      <concept>
        <code value="ORPHA:99856" />
        <display value="Primary syringomyelia" />
      </concept>
      <concept>
        <code value="ORPHA:99857" />
        <display value="Secondary syringomyelia" />
      </concept>
      <concept>
        <code value="ORPHA:99858" />
        <display value="Idiopathic syringomyelia" />
      </concept>
      <concept>
        <code value="ORPHA:99860" />
        <display value="Precursor B-cell acute lymphoblastic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:99861" />
        <display value="Precursor T-cell acute lymphoblastic leukemia" />
      </concept>
      <concept>
        <code value="ORPHA:99865" />
        <display value="Spermatocytic seminoma" />
      </concept>
      <concept>
        <code value="ORPHA:99867" />
        <display value="Thymoma" />
      </concept>
      <concept>
        <code value="ORPHA:99868" />
        <display value="Thymic carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:99869" />
        <display value="Thymic neuroendocrine carcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:99870" />
        <display value="Letterer-Siwe disease" />
      </concept>
      <concept>
        <code value="ORPHA:99871" />
        <display value="Eosinophilic granuloma" />
      </concept>
      <concept>
        <code value="ORPHA:99872" />
        <display value="Hashimoto-Pritzker syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99873" />
        <display value="Hand-Schuller-Christian disease" />
      </concept>
      <concept>
        <code value="ORPHA:99874" />
        <display value="Adult pulmonary Langerhans cell histiocytosis" />
      </concept>
      <concept>
        <code value="ORPHA:99875" />
        <display value="Ehlers-Danlos syndrome type 7A" />
      </concept>
      <concept>
        <code value="ORPHA:99876" />
        <display value="Ehlers-Danlos syndrome type 7B" />
      </concept>
      <concept>
        <code value="ORPHA:99877" />
        <display value="Familial parathyroid adenoma" />
      </concept>
      <concept>
        <code value="ORPHA:99878" />
        <display value="Primary parathyroid hyperplasia" />
      </concept>
      <concept>
        <code value="ORPHA:99879" />
        <display value="Familial isolated hyperparathyroidism" />
      </concept>
      <concept>
        <code value="ORPHA:99880" />
        <display value="Hyperparathyroidism-jaw tumor syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99885" />
        <display value="Permanent neonatal diabetes mellitus" />
      </concept>
      <concept>
        <code value="ORPHA:99886" />
        <display value="Transient neonatal diabetes mellitus" />
      </concept>
      <concept>
        <code value="ORPHA:99887" />
        <display value="Acute megakaryoblastic leukemia in Down syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99889" />
        <display value="Cushing syndrome due to ectopic ACTH secretion" />
      </concept>
      <concept>
        <code value="ORPHA:99892" />
        <display value="ACTH-dependent Cushing syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99893" />
        <display value="ACTH-independent Cushing syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99898" />
        <display value="Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:999" />
        <display value="Ermine phenotype" />
      </concept>
      <concept>
        <code value="ORPHA:99900" />
        <display value="Long chain acyl-CoA dehydrogenase deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:99901" />
        <display value="Acyl-CoA dehydrogenase 9 deficiency" />
      </concept>
      <concept>
        <code value="ORPHA:99903" />
        <display value="Spirillary rat-bite fever" />
      </concept>
      <concept>
        <code value="ORPHA:99905" />
        <display value="Streptobacillary rat-bite fever" />
      </concept>
      <concept>
        <code value="ORPHA:99906" />
        <display value="Farmers lung disease" />
      </concept>
      <concept>
        <code value="ORPHA:99907" />
        <display value="House allergic alveolitis" />
      </concept>
      <concept>
        <code value="ORPHA:99908" />
        <display value="Pigeon-breeder lung disease" />
      </concept>
      <concept>
        <code value="ORPHA:99909" />
        <display value="Occupational allergic alveolitis" />
      </concept>
      <concept>
        <code value="ORPHA:99912" />
        <display value="Malignant dysgerminomatous germ cell tumor of the ovary" />
      </concept>
      <concept>
        <code value="ORPHA:99913" />
        <display value="Extragonadal non-dysgerminomatous germ cell tumor" />
      </concept>
      <concept>
        <code value="ORPHA:99914" />
        <display value="Gynandroblastoma" />
      </concept>
      <concept>
        <code value="ORPHA:99915" />
        <display value="Maligant granulosa cell tumor of the ovary" />
      </concept>
      <concept>
        <code value="ORPHA:99916" />
        <display value="Malignant Sertoli-Leydig cell tumor of the ovary" />
      </concept>
      <concept>
        <code value="ORPHA:99917" />
        <display value="Theca steroid-producing cell malignant tumor of ovary, not further specified" />
      </concept>
      <concept>
        <code value="ORPHA:99918" />
        <display value="Streptococcal toxic-shock syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99919" />
        <display value="Staphylococcal toxic-shock syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99920" />
        <display value="Acute graft versus host disease" />
      </concept>
      <concept>
        <code value="ORPHA:99921" />
        <display value="Chronic graft versus host disease" />
      </concept>
      <concept>
        <code value="ORPHA:99922" />
        <display value="Ocular cicatricial pemphigoid" />
      </concept>
      <concept>
        <code value="ORPHA:99925" />
        <display value="Invasive mole" />
      </concept>
      <concept>
        <code value="ORPHA:99926" />
        <display value="Gestational choriocarcinoma" />
      </concept>
      <concept>
        <code value="ORPHA:99927" />
        <display value="Hydatidiform mole" />
      </concept>
      <concept>
        <code value="ORPHA:99928" />
        <display value="Placental site trophoblastic tumor" />
      </concept>
      <concept>
        <code value="ORPHA:99930" />
        <display value="Secondary pulmonary hemosiderosis" />
      </concept>
      <concept>
        <code value="ORPHA:99931" />
        <display value="Idiopathic pulmonary hemosiderosis" />
      </concept>
      <concept>
        <code value="ORPHA:99932" />
        <display value="Heiner syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99933" />
        <display value="Pleuropulmonary blastoma type 1" />
      </concept>
      <concept>
        <code value="ORPHA:99934" />
        <display value="Pleuropulmonary blastoma type 2" />
      </concept>
      <concept>
        <code value="ORPHA:99935" />
        <display value="Pleuropulmonary blastoma type 3" />
      </concept>
      <concept>
        <code value="ORPHA:99936" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2B" />
      </concept>
      <concept>
        <code value="ORPHA:99937" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2C" />
      </concept>
      <concept>
        <code value="ORPHA:99938" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2D" />
      </concept>
      <concept>
        <code value="ORPHA:99939" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2E" />
      </concept>
      <concept>
        <code value="ORPHA:99940" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2F" />
      </concept>
      <concept>
        <code value="ORPHA:99941" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2G" />
      </concept>
      <concept>
        <code value="ORPHA:99942" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2I" />
      </concept>
      <concept>
        <code value="ORPHA:99943" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2J" />
      </concept>
      <concept>
        <code value="ORPHA:99944" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2K" />
      </concept>
      <concept>
        <code value="ORPHA:99945" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2L" />
      </concept>
      <concept>
        <code value="ORPHA:99946" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2A1" />
      </concept>
      <concept>
        <code value="ORPHA:99947" />
        <display value="Autosomal dominant Charcot-Marie-Tooth disease type 2A2" />
      </concept>
      <concept>
        <code value="ORPHA:99948" />
        <display value="Charcot-Marie-Tooth disease type 4A" />
      </concept>
      <concept>
        <code value="ORPHA:99949" />
        <display value="Charcot-Marie-Tooth disease type 4C" />
      </concept>
      <concept>
        <code value="ORPHA:99950" />
        <display value="Charcot-Marie-Tooth disease type 4D" />
      </concept>
      <concept>
        <code value="ORPHA:99951" />
        <display value="Charcot-Marie-Tooth disease type 4E" />
      </concept>
      <concept>
        <code value="ORPHA:99952" />
        <display value="Charcot-Marie-Tooth disease type 4F" />
      </concept>
      <concept>
        <code value="ORPHA:99953" />
        <display value="Charcot-Marie-Tooth disease type 4G" />
      </concept>
      <concept>
        <code value="ORPHA:99954" />
        <display value="Charcot-Marie-Tooth disease type 4H" />
      </concept>
      <concept>
        <code value="ORPHA:99955" />
        <display value="Charcot-Marie-Tooth disease type 4B1" />
      </concept>
      <concept>
        <code value="ORPHA:99956" />
        <display value="Charcot-Marie-Tooth disease type 4B2" />
      </concept>
      <concept>
        <code value="ORPHA:99960" />
        <display value="Benign recurrent intrahepatic cholestasis type 1" />
      </concept>
      <concept>
        <code value="ORPHA:99961" />
        <display value="Benign recurrent intrahepatic cholestasis type 2" />
      </concept>
      <concept>
        <code value="ORPHA:99965" />
        <display value="OSullivan-McLeod syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99966" />
        <display value="Atypical teratoid rhabdoid tumor" />
      </concept>
      <concept>
        <code value="ORPHA:99967" />
        <display value="Myxoid/round cell liposarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:99969" />
        <display value="Pleomorphic liposarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:99970" />
        <display value="Dedifferentiated liposarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:99971" />
        <display value="Well-differentiated liposarcoma" />
      </concept>
      <concept>
        <code value="ORPHA:99976" />
        <display value="Adenocarcinoma of the esophagus" />
      </concept>
      <concept>
        <code value="ORPHA:99977" />
        <display value="Squamous cell carcinoma of the esophagus" />
      </concept>
      <concept>
        <code value="ORPHA:99978" />
        <display value="Klatskin tumor" />
      </concept>
      <concept>
        <code value="ORPHA:99981" />
        <display value="Apnea of prematurity" />
      </concept>
      <concept>
        <code value="ORPHA:99983" />
        <display value="Cutaneous myiasis" />
      </concept>
      <concept>
        <code value="ORPHA:99989" />
        <display value="Intermediate DEND syndrome" />
      </concept>
      <concept>
        <code value="ORPHA:99990" />
        <display value="Brill-Zinsser disease" />
      </concept>
      <concept>
        <code value="ORPHA:99991" />
        <display value="Relapsing epidemic typhus" />
      </concept>
      <concept>
        <code value="ORPHA:99994" />
        <display value="Complex regional pain syndrome type 2" />
      </concept>
      <concept>
        <code value="ORPHA:99995" />
        <display value="Complex regional pain syndrome type 1" />
      </concept>
    </include>
  </compose>
</ValueSet>

name : ValueSet-Genomics-ConditionCode-1

{

}

<name value="ValueSet-Genomics-ConditionCode-1" />