SIMPLIFIER.NET - FHIRPath Playground

FHIRPath

If you Log in or sign up, you can edit this script yourself.

{
  "resourceType": "ValueSet",
  "id": "2.16.840.1.113883.2.4.11.196--20191010091229",
  "meta": {
    "profile": [
      "http://hl7.org/fhir/StructureDefinition/shareablevalueset"
    ]
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/resource-effectivePeriod",
      "valuePeriod": {
        "start": "2019-10-10T08:12:29+00:00"
      }
    }
  ],
  "url": "http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.11.196--20191010091229",
  "identifier": [
    {
      "use": "official",
      "system": "http://art-decor.org/ns/oids/vs",
      "value": "2.16.840.1.113883.2.4.11.196"
    }
  ],
  "version": "2.3.0",
  "name": "CongenitaleAfwijking22",
  "title": "Congenitale afwijking",
  "status": "active",
  "experimental": false,
  "publisher": "KNOV",
  "description": "Congenitale afwijking",
  "immutable": false,
  "copyright": "This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org.",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "concept": [
          {
            "code": "276508000",
            "display": "Hydrops foetalis"
          },
          {
            "code": "88425004",
            "display": "Congenital anomaly of nervous system (disorder)"
          },
          {
            "code": "609417004",
            "display": "Fetal anencephaly (disorder)"
          },
          {
            "code": "431265009",
            "display": "Fetal microcephaly (disorder)"
          },
          {
            "code": "76916001",
            "display": "Spina bifida occulta (disorder)"
          },
          {
            "code": "414667000",
            "display": "Meningomyelocele (disorder)"
          },
          {
            "code": "171131006",
            "display": "Meningocele (disorder)"
          },
          {
            "code": "47032000",
            "display": "Congenital hydrocephalus (disorder)"
          },
          {
            "code": "30915001",
            "display": "Holoprosencephaly sequence (disorder)"
          },
          {
            "code": "55999004",
            "display": "Encephalocele (disorder)"
          },
          {
            "code": "363222009",
            "display": "Neonatal neuromuscular disorder (disorder)"
          },
          {
            "code": "19416009",
            "display": "Congenital anomaly of eye (disorder)"
          },
          {
            "code": "61142002",
            "display": "Microphthalmos (disorder)"
          },
          {
            "code": "275259005",
            "display": "Congenital malformation of ear (disorder)"
          },
          {
            "code": "9904008",
            "display": "Congenital anomaly of cardiovascular system (disorder)"
          },
          {
            "code": "204470001",
            "display": "Single umbilical artery (disorder)"
          },
          {
            "code": "204296002",
            "display": "Discordant ventriculoarterial connection (disorder)"
          },
          {
            "code": "86299006",
            "display": "Tetralogy of Fallot (disorder)"
          },
          {
            "code": "30288003",
            "display": "Ventricular septal defect (disorder)"
          },
          {
            "code": "62067003",
            "display": "Hypoplastic left heart syndrome (disorder)"
          },
          {
            "code": "7305005",
            "display": "Coarctation of aorta (disorder)"
          },
          {
            "code": "4374004",
            "display": "Congenital anomaly of tricuspid valve (disorder)"
          },
          {
            "code": "94702005",
            "display": "Multiple congenital cardiac defects (disorder)"
          },
          {
            "code": "95470009",
            "display": "Congenital anomaly of digestive tract (disorder)"
          },
          {
            "code": "80281008",
            "display": "Cleft lip (disorder)"
          },
          {
            "code": "87979003",
            "display": "Cleft palate (disorder)"
          },
          {
            "code": "69771008",
            "display": "Congenital anomaly of esophagus (disorder)"
          },
          {
            "code": "84296002",
            "display": "Congenital atresia of small intestine (disorder)"
          },
          {
            "code": "204711007",
            "display": "Atresia of large intestine (disorder)"
          },
          {
            "code": "204712000",
            "display": "Anal atresia (disorder)"
          },
          {
            "code": "204739008",
            "display": "Hirschsprung's disease (disorder)"
          },
          {
            "code": "29980002",
            "display": "Congenital malrotation of intestine (disorder)"
          },
          {
            "code": "9707006",
            "display": "Intestinal volvulus (disorder)"
          },
          {
            "code": "77868001",
            "display": "Congenital anomaly of respiratory system (disorder)"
          },
          {
            "code": "204508009",
            "display": "Choanal atresia (disorder)"
          },
          {
            "code": "14532008",
            "display": "Congenital anomaly of trachea (disorder)"
          },
          {
            "code": "80825009",
            "display": "Congenital hypoplasia of lung (disorder)"
          },
          {
            "code": "66987001",
            "display": "Congenital lobar emphysema (disorder)"
          },
          {
            "code": "111318005",
            "display": "Congenital cystic adenomatoid malformation of lung (disorder)"
          },
          {
            "code": "79231000",
            "display": "Hydrothorax (disorder)"
          },
          {
            "code": "83035003",
            "display": "Chylothorax (disorder)"
          },
          {
            "code": "17190001",
            "display": "Congenital diaphragmatic hernia (disorder)"
          },
          {
            "code": "21524000",
            "display": "Relaxation of diaphragm (disorder)"
          },
          {
            "code": "287085006",
            "display": "Genitourinary congenital anomalies (disorder)"
          },
          {
            "code": "416010008",
            "display": "Hypospadias (disorder)"
          },
          {
            "code": "406476007",
            "display": "Epispadias (disorder)"
          },
          {
            "code": "204878001",
            "display": "Undescended testicle (disorder)"
          },
          {
            "code": "61758007",
            "display": "Exstrophy of bladder sequence (disorder)"
          },
          {
            "code": "41962002",
            "display": "Oligohydramnios sequence (disorder)"
          },
          {
            "code": "82525005",
            "display": "Congenital cystic kidney disease (disorder)"
          },
          {
            "code": "7163005",
            "display": "Urinary tract obstruction (disorder)"
          },
          {
            "code": "39179006",
            "display": "Disorder of sexual differentiation (disorder)"
          },
          {
            "code": "199879009",
            "display": "Congenital anomaly of skin (disorder)"
          },
          {
            "code": "93471006",
            "display": "Hemangioma of skin (disorder)"
          },
          {
            "code": "398943008",
            "display": "Congenital pigmented melanocytic nevus of skin (disorder)"
          },
          {
            "code": "81336004",
            "display": "Congenital anomaly of abdominal wall (disorder)"
          },
          {
            "code": "72951007",
            "display": "Gastroschisis (disorder)"
          },
          {
            "code": "18735004",
            "display": "Congenital omphalocele (disorder)"
          },
          {
            "code": "396347007",
            "display": "Umbilical hernia (disorder)"
          },
          {
            "code": "429200006",
            "display": "Congenital inguinal hernia (disorder)"
          },
          {
            "code": "73573004",
            "display": "Congenital anomaly of musculoskeletal system (disorder)"
          },
          {
            "code": "367506006",
            "display": "Polydactyly (disorder)"
          },
          {
            "code": "373413006",
            "display": "Syndactyly (disorder)"
          },
          {
            "code": "302297009",
            "display": "Congenital deformity of foot (disorder)"
          },
          {
            "code": "45806008",
            "display": "Reduction deformity of upper limb (disorder)"
          },
          {
            "code": "77595004",
            "display": "Reduction deformity of lower limb (disorder)"
          },
          {
            "code": "36172001",
            "display": "Congenital subluxation of hip (disorder)"
          },
          {
            "code": "276720006",
            "display": "Dysmorphism (disorder)"
          },
          {
            "code": "43876007",
            "display": "Situs inversus viscerum (disorder)"
          },
          {
            "code": "444406006",
            "display": "Multiple congenital anomalies (disorder)"
          },
          {
            "code": "82354003",
            "display": "Multiple system malformation syndrome (disorder)"
          },
          {
            "code": "217710005",
            "display": "Congenital iodine deficiency syndrome (disorder)"
          },
          {
            "code": "86095007",
            "display": "Inborn error of metabolism (disorder)"
          },
          {
            "code": "363346000:246454002=255399007",
            "display": "Congenital malignant neoplastic disease (disorder)"
          }
        ]
      },
      {
        "system": "http://hl7.org/fhir/v3/NullFlavor",
        "concept": [
          {
            "code": "OTH",
            "display": "Overig"
          },
          {
            "code": "NI",
            "display": "Geen informatie"
          }
        ]
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "concept": [
          {
            "code": "09",
            "display": "Overige congenitale afwijkingen zenuwstelsel"
          },
          {
            "code": "B",
            "display": "Zintuigen"
          },
          {
            "code": "11",
            "display": "Overige congenitale afwijkingen ogen"
          },
          {
            "code": "13",
            "display": "Overige congenitale afwijkingen zintuigen"
          },
          {
            "code": "22",
            "display": "Overige congenitale afwijking hart en bloedvaten"
          },
          {
            "code": "30",
            "display": "Overige congenitale afwijking tractus digestivus"
          },
          {
            "code": "38",
            "display": "Overige congenitale afwijking tractus respiratorius"
          },
          {
            "code": "69",
            "display": "Overige congenitale afwijking tractus urogenitalis"
          },
          {
            "code": "74",
            "display": "Overige congenitale huidafwijking"
          },
          {
            "code": "85",
            "display": "Overige congenitale afwijking buikwand"
          },
          {
            "code": "96",
            "display": "Overige congenitale afwijking extremiteiten"
          },
          {
            "code": "98",
            "display": "Overige congenitale afwijking skelet en spierstelsel"
          },
          {
            "code": "J",
            "display": "Multipele/syndromale congenitale afwijkingen (niet chromosomaal)"
          },
          {
            "code": "104",
            "display": "Overige multipele/syndromale afwijkingen"
          },
          {
            "code": "K",
            "display": "Overige congenitale afwijkingen"
          },
          {
            "code": "112",
            "display": "Andere endocrinologische afwijkingen"
          }
        ]
      }
    ]
  },
  "expansion": {
    "identifier": "urn:uuid:c39b2d0d-61bb-40c9-a14f-25e345f53871",
    "timestamp": "2020-11-23T14:39:43.978+00:00",
    "total": 93,
    "contains": [
      {
        "system": "http://snomed.info/sct",
        "code": "276508000",
        "display": "Hydrops foetalis"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "88425004",
        "display": "Congenital anomaly of nervous system (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "609417004",
        "display": "Fetal anencephaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "431265009",
        "display": "Fetal microcephaly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "76916001",
        "display": "Spina bifida occulta (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "414667000",
        "display": "Meningomyelocele (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "171131006",
        "display": "Meningocele (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "47032000",
        "display": "Congenital hydrocephalus (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "30915001",
        "display": "Holoprosencephaly sequence (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "55999004",
        "display": "Encephalocele (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "363222009",
        "display": "Neonatal neuromuscular disorder (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "09",
        "display": "Overige congenitale afwijkingen zenuwstelsel"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "B",
        "display": "Zintuigen"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "19416009",
        "display": "Congenital anomaly of eye (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "61142002",
        "display": "Microphthalmos (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "11",
        "display": "Overige congenitale afwijkingen ogen"
      },
      {
        "system": "http://snomed.info/sct",
        "inactive": true,
        "code": "8380000",
        "display": "Congenital anomaly of ear (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "275259005",
        "display": "Congenital malformation of ear (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "13",
        "display": "Overige congenitale afwijkingen zintuigen"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "9904008",
        "display": "Congenital anomaly of cardiovascular system (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "204470001",
        "display": "Single umbilical artery (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "204296002",
        "display": "Discordant ventriculoarterial connection (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "86299006",
        "display": "Tetralogy of Fallot (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "30288003",
        "display": "Ventricular septal defect (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "62067003",
        "display": "Hypoplastic left heart syndrome (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "7305005",
        "display": "Coarctation of aorta (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "4374004",
        "display": "Congenital anomaly of tricuspid valve (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "94702005",
        "display": "Multiple congenital cardiac defects (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "22",
        "display": "Overige congenitale afwijking hart en bloedvaten"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "95470009",
        "display": "Congenital anomaly of digestive tract (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "80281008",
        "display": "Cleft lip (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "87979003",
        "display": "Cleft palate (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "69771008",
        "display": "Congenital anomaly of esophagus (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "84296002",
        "display": "Congenital atresia of small intestine (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "204711007",
        "display": "Atresia of large intestine (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "204712000",
        "display": "Anal atresia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "204739008",
        "display": "Hirschsprung's disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "29980002",
        "display": "Congenital malrotation of intestine (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "9707006",
        "display": "Intestinal volvulus (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "30",
        "display": "Overige congenitale afwijking tractus digestivus"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "77868001",
        "display": "Congenital anomaly of respiratory system (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "204508009",
        "display": "Choanal atresia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "14532008",
        "display": "Congenital anomaly of trachea (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "80825009",
        "display": "Congenital hypoplasia of lung (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "66987001",
        "display": "Congenital lobar emphysema (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "111318005",
        "display": "Congenital cystic adenomatoid malformation of lung (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "79231000",
        "display": "Hydrothorax (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "83035003",
        "display": "Chylothorax (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "17190001",
        "display": "Congenital diaphragmatic hernia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "21524000",
        "display": "Relaxation of diaphragm (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "38",
        "display": "Overige congenitale afwijking tractus respiratorius"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "287085006",
        "display": "Genitourinary congenital anomalies (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "416010008",
        "display": "Hypospadias (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "406476007",
        "display": "Epispadias (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "204878001",
        "display": "Undescended testicle (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "61758007",
        "display": "Exstrophy of bladder sequence (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "41962002",
        "display": "Oligohydramnios sequence (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "82525005",
        "display": "Congenital cystic kidney disease (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "7163005",
        "display": "Urinary tract obstruction (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "39179006",
        "display": "Disorder of sexual differentiation (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "69",
        "display": "Overige congenitale afwijking tractus urogenitalis"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "199879009",
        "display": "Congenital anomaly of skin (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "93471006",
        "display": "Hemangioma of skin (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "398943008",
        "display": "Congenital pigmented melanocytic nevus of skin (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "74",
        "display": "Overige congenitale huidafwijking"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "81336004",
        "display": "Congenital anomaly of abdominal wall (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "72951007",
        "display": "Gastroschisis (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "18735004",
        "display": "Congenital omphalocele (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "396347007",
        "display": "Umbilical hernia (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "429200006",
        "display": "Congenital inguinal hernia (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "85",
        "display": "Overige congenitale afwijking buikwand"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "73573004",
        "display": "Congenital anomaly of musculoskeletal system (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "367506006",
        "display": "Polydactyly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "373413006",
        "display": "Syndactyly (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "302297009",
        "display": "Congenital deformity of foot (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "45806008",
        "display": "Reduction deformity of upper limb (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "77595004",
        "display": "Reduction deformity of lower limb (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "96",
        "display": "Overige congenitale afwijking extremiteiten"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "36172001",
        "display": "Congenital subluxation of hip (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "98",
        "display": "Overige congenitale afwijking skelet en spierstelsel"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "J",
        "display": "Multipele/syndromale congenitale afwijkingen (niet chromosomaal)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "276720006",
        "display": "Dysmorphism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "43876007",
        "display": "Situs inversus viscerum (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "444406006",
        "display": "Multiple congenital anomalies (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "82354003",
        "display": "Multiple system malformation syndrome (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "104",
        "display": "Overige multipele/syndromale afwijkingen"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "K",
        "display": "Overige congenitale afwijkingen"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "217710005",
        "display": "Congenital iodine deficiency syndrome (disorder)"
      },
      {
        "system": "urn:oid:2.16.840.1.113883.2.4.4.13.8",
        "code": "112",
        "display": "Andere endocrinologische afwijkingen"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "86095007",
        "display": "Inborn error of metabolism (disorder)"
      },
      {
        "system": "http://snomed.info/sct",
        "code": "363346000:246454002=255399007",
        "display": "Congenital malignant neoplastic disease (disorder)"
      },
      {
        "system": "http://hl7.org/fhir/v3/NullFlavor",
        "code": "OTH",
        "display": "Overig"
      },
      {
        "system": "http://hl7.org/fhir/v3/NullFlavor",
        "code": "NI",
        "display": "Geen informatie"
      }
    ]
  }
}

name : CongenitaleAfwijking22

{

}