CodeSystem MDS Question Tag Genomics

Usage

A set of codes used to map MDS Dataset to FHIR Resources.This is intended to be used on Resource.meta.tag.

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Concepts

This code system https://fhir.nhs.uk/CodeSystem/mds-questiontag-genomics defines the following codes:

LvlCodeDisplayDefinition
1datagroup-healthcare-professionalHealthcare ProfessionalData group - Healthcare professional
2  HCP-1HCP - Genomic test order roleHCP's function within the genomic test ordering process
2  HCP-2HCP - First nameHCP's first name.
2  HCP-13HCP - surnameHCP'surname
2  HCP-3HCP - Job titleHCP's job title.
2  HCP-4HCP - Current specialtyHCP's current specialty.
2  HCP-5HCP - Telephone numberHCP's telephone number.
2  HCP-6HCP - Email addressHCP's email address.
2  HCP-7HCP - Organisation nameHCP's requesting organisation name.
2  HCP-9HCP - Organisation ODS codeHCP's organisation ODS code
2  HCP-10HCP - Department nameHCP's department name.
2  HCP-11HCP - Professional registration numberHCP's professional registration number such as their GMC number.
2  HCP-12HCP - Professional registration number typeHCP's professional registration number type such as 'GMC'.
1datagroup-patientPatientData group - Patient
2  P-1Patient - TitlePatient's title.
2  P-2Patient - First namePatient's first name.
2  P-40Patient - MiddlenamePatient's middle name.
2  P-3Patient - SurnamePatient's last name.
2  P-41Patient - Name useLinks each patient name entry to confirm if current, previous or what the patient is known as.
2  P-4Patient - Date of birthPatient's date of birth.
2  P-6Patient - PostcodePatient's home postcode.
2  P-7Patient - Country of residencePatient's home country.
2  P-9Patient - EthnicityPatient's ethnicity.
2  P-10Patient - Sex defined at birthPatient's phenotypic sex classification as defined at birth based on physical characteristic.
2  P-12Patient - GP practice's ODS CodePatient's GP practice ODS code.
2  P-13Patient - Is from consanguineous unionThe fact of the patient's biological parents being descended from the same ancestor.
2  P-15Patient - NHS numberPatient's NHS number.
2  P-16Patient - Local identifierPatient's identification code other than NHS number.
2  P-42Patient - ODS code of organisation which assigned local identifierODS code of the organisation which assigned the local identifier P-16.
2  P-17Patient - Reason for unavailable NHS numberReason for an NHS number not being provided.
2  P-18Patient - Relationship to probandThis patient's relationship to the primary patient.
2  P-19Patient - Gender IdentityPatient's stated gender, determined by the patient.
2  P-20Patient - Deceased datePatient's date of death.
2  P-21Patient - Chromosomal sexPatient's genomic / karyotypic characteristic. Determined by genomic testing.
2  P-35Patient - Withheld identity reasonConfirmation why the patient is withholding identity details.
2  P-37Patient - Local Pedigree / Family identifierPatient's pedigree or family identifying id.
2  P-39Patient - Reason for inclusion in genomic test requestReason patient has been included in genomic test request, such as to support proband testing or providing own genomic reporting
1datagroup-fetusFetusData group - Fetus
2  F-1Fetus - Local identifierFetus' identification code other than NHS number.
2  F-7Fetus - ODS code of organisation which assigned local identifierODS code of the organisation which assigned the local identifier F-1.
2  F-2Fetus - Observed sexFetus' phenotypic sex classification. Estimated physical characteristic. Currently determined by ultrasound. Gender for PLCM.
2  F-3Fetus - Chromosomal sexFetus' genomic / karyotypic characteristic. Determined by genomic testing.
2  F-6Fetus - Life status at time of requestFetus' alive or deceased status details at the point of test ordering.
2  F-8Fetus - Pregnancy idThe id of a given pregnancy which this fetus belongs to.
1datagroup-test-requestTest RequestData group - Test Request
2  TR-2Test Request - Payment statusHow the test request is funded
2  TR-4Test Request - Requesting reason rare diseaseThe reason for a rare disease genomic test.
2  TR-38Test Request - Requesting reason cancerThe reason for a cancer genomic test.
2  TR-5Test Request - High level test identifierLegacy high level ids which identify the requested test. Options provided by old Test Directory.
2  TR-6Test Request - High level test identifier descriptionLegacy high level name of the id requested
2  TR-7Test Request - Low level test identifierThe low level CITT code which identifies the requested test. Options provided by Test Directory (TEST IDENTIFIER OR TEST CODE).
2  TR-8Test Request - Low level test identifier descriptionThe low level CITT name of the considered test.
2  TR-9Test Request - Low level multipurpose test identifierThe low level code which identifies the test to be actioned when the CITT code is multipurpose (CLINICAL INDICATION).
2  TR-10Test Request - Low level multipurpose test identifier descriptionThe low level name of the test to be actioned when the CITT code is multipurpose.
2  TR-21Test Request - Genomic package idId of the package requested.
2  TR-22Test Request - Genomic package nameName of the package requested.
2  TR-23Test Request - Genomic package versionVersion of the package requested.
2  TR-24Test Request - Genomic test idId of the test requested.
2  TR-25Test Request - Genomic test nameName of the test requested.
2  TR-26Test Request - Genomic test versionVersion of the test requested.
2  TR-27Test Request - Additional panelsAdditional panels to test.
2  TR-28Test request - Target typeType of target to test.
2  TR-29Test request - Target detailDetail of target to test.
2  TR-11Test Request - Count of patients to be testedCount of patients to be tested including the proband/primary patient.
2  TR-12Test Request - Urgency reasonThe test request urgency reason.
2  TR-13Test Request - Reanalysis reasonThe reason reanalysis has been requested.
2  TR-14Test Request - Detail of reason for requestFurther detail associated to the reason reanalysis has been requested.
2  TR-15Test Request - Type of reanalysisThe type of reanalysis which has been requested.
2  TR-17Test Request - Is urgentConfirmation if the test request is urgent.
2  TR-35Test Request - Purpose of linkingThe reason a given test request has been linked to another test request.
2  TR-36Test Request - Central email address for reportingCentral email address for contingency in the event of not being able to obtain a report via the requester.
2  TR-20Test Request - Genomic report delivery methodTest Request - Genomic report delivery method
2  TR-30Test Request - Add private genomic request and report to NHS recordConfirmation if the content of a private genomic test request should be added to an NHS record.
2  TR-31Test Request - Test request form versionVersion of the test order form completed and submitted.
2  TR-32Test Request - File / Link to fileUpload of a file or a link to a file for adding documents such as previous genomic reports to a test order.
2  TR-33Test Request - File detailDetail to provide context to an uploaded file or document link.
2  TR-34Test Request - Clinical utilityClinical benefit to patient of obtaining a requested genomic report.
2  TR-39Test Request - Linked test request referenceThe reference to any associated test requests
1datagroup-ngrl-consentNGRL-consentData group - NGRL consent
2  NGRL-1NGRL consent - Date of NGRL consentThe date NGRL consent was provided.
2  NGRL-2NGRL consent - Patient has made their own choice to consent to the NGRLConfirmation if the patient to be tested has provided NGRL consent themselves.
2  NGRL-3NGRL consent - Patient representative name (if patient cannot make their own choice)The name of the patient representative.
2  NGRL-4NGRL consent - I confirm that the patient (or their representative) agree to have their genomic and healthcare data used for researchThe outcome of the patient or their representative’s choice in consenting to including their data used for research in the NGRL.
2  NGRL-5NGRL consent - NGRL consent document linkA URL where a copy of a completed NGRL consent form may be found.
1datagroup-primary-samplePrimary SampleData group - Primary Sample
2  PS-2Primary Sample - Local identifierLocal ids applied to a sample
2  PS-3Primary Sample - ODS code of organisation which assigned local idODS code of the organisation which assigned the local sample id.
2  PS-10Primary Sample - Obtained dateDate at which a specimen/biopsy was obtained from patient.
2  PS-11Primary Sample - Primary sampleThe primary sample material.
2  PS-12Primary Sample - Primary sample stateThe state of the primary sample.
2  PS-25Primary Sample - Preservative/ContainerHow the primary sample is preserved.
2  PS-30Primary Sample - Block identifierSample block identifier
2  PS-31Primary Sample - Fixative typeSample fixative type
2  PS-32Primary Sample - Hours to fixationSample hours to fixation
2  PS-33Primary Sample - Hours in fixativeSample hours in fixative
2  PS-34Primary Sample - Tumour enrichment methodMethod used for tumour enrichment.
2  PS-13Primary Sample - Necrosis% necrotic (dead) cells in primary sample.
2  PS-14Primary Sample - Nucleated cell countNucleated (with nucleous) cell (non tumour and tumour) count in the primary sample (Solid Tumour and Haem-Onc).
2  PS-15Primary Sample - Tumour nuclear content in whole sectionNeoplastic (tumour) cell content in the primary sample whole section(Solid Tumour) - sourced at local lab. (%)
2  PS-26Primary Sample - Tumour nuclear content in marked areaNeoplastic (tumour) cell content in the primary sample marked area(Solid Tumour) - sourced at local lab. (%)
2  PS-17Primary Sample - Solid tumour morphologyThe histology and likely course of development of a tumour.
2  PS-18Primary Sample - Solid tumour topographyThe tumour sample site. e.g. from colon, stomach etc.
2  PS-29Primary Sample - Is biopsyPrimary Sample - Is biopsy
2  PS-19Primary Sample - Biopsy siteDigital confirmation that the sample is a biopsy.
2  PS-21Primary Sample - Observed maternal cell contamination (MCC)An observed outcome which may indicate MCC
2  PS-27Primary Sample - Test confirmed maternal cell contamination (MCC)Analytically confirmed MCC levels
2  PS-22Primary Sample - Option for all products of conceptionPrimary Sample - Option for all products of conception
2  PS-23Primary Sample - Blasts %Future management for products of conception.
2  PS-24Primary Sample - High infection risk reasonThe high contamination risk reason for a primary sample.
2  PS-28Primary Sample - Patient life status at the time of collectionIf the patient was alive or deceased at the point of collecting a sample.
2  PS-35Primary Sample - Solid tumour typeThe origin or context of a tumour sample.
1datagroup-patient-clinical-informationPatient Clinical InformationData group - Patient Clinical Information
2  PCI-1Patient clinical information - Genomic EthnicityPatient's ethnicity where 'Patient - Ethnicity field' doesn't provide an adequate description. E.g Ashkenazi Jewish
2  PCI-2Patient clinical information - Disease StatusIf the patient is affected, unaffected, or it is unknown.
2  PCI-4Patient clinical information - Age at disease onsetThe age when a change in patients' health was first noted in line with suspected diagnosis.
2  PCI-5Patient clinical information - Known/Suspected DiseaseDisease a patient is believed, known to have, or be at risk of developing.
2  PCI-6Patient clinical information - Phenotypic detailsThe HPO (or alternative ontology as appropriate) term names for the observable disease traits.
2  PCI-7Patient clinical information - SymptomsThe patient's symptoms
2  PCI-10Patient clinical information - Count of tumoursHow many tumours the patient has.
2  PCI-11Patient clinical information - Site of tumourLocation of the tumours on the body.
2  PCI-14Patient clinical information - Tumour sites - Body image diagramImage attachment of body with tumour sites highlighted.
2  PCI-15Patient clinical information - Pedigree details / Relevant family historyThe patient's pedigree/family history details (inc family history of cancer).
2  PCI-16Patient clinical information - Pedigree diagramImage attachment of pedigree details
2  PCI-17Patient clinical information - Laterality of hearing lossLaterality of the hearing loss i.e. bilateral or unilateral.
2  PCI-18Patient clinical information - Fetal haemoglobinopathy maternal screening genotypeMaternal screening genotype for haemoglobinopathy testing.
2  PCI-21Patient clinical information - Legal considerationsLegal considerations for a given request.
2  PCI-22Patient clinical information - Fetal haemoglobinopathy paternal screening genotypePaternal screening genotype for haemoglobinopathy testing
2  PCI-23Patient clinical information - Expected Maternity Unit - Organisation nameRequesting clinician's organisation name.
2  PCI-24Patient clinical information - Expected Maternity Unit - Organisation addressRequesting clinician's organisation address.
2  PCI-25Patient clinical information - Expected Maternity Unit - Organisation ODS codeRequesting clinician's organisation ODS code.
2  PCI-26Patient clinical information - Expected Maternity Unit - Department nameRequesting clinician's department name.
2  PCI-27Patient clinical information - Growth historySummary passage of text to highlight patient centile history e.g. head circumference, weight, etc.
2  PCI-28Patient clinical information - Severity of hearing lossFree text regarding hearing loss
2  PCI-29Patient clinical information - Retinal degenerationFree text regarding retinal degeneration
2  PCI-30Patient clinical information - Risk factorsToxic medication - Prematurity (risk factor for hearing loss) e.g. Baby early birth - Ototoxic medication.
2  PCI-31Patient clinical information - Suspected inborn error type(s)Suspected inborn error type(s)
2  PCI-32Patient clinical information - Abnormal infection history siteAbnormal infection history site organism
2  PCI-33Patient clinical information - Abnormal infection history site organismAbnormal infection history site organism
2  PCI-34Is on ig replacementIf the patient is on immunoglobin replacement treatment.
2  PCI-35Patient clinical information - Current and previous treatment detailDetail regarding relevant current and previous medical treatments.
2  PCI-36Patient clinical information - Pregnancy statusPatient`s pregnancy status
2  PCI-37Patient clinical information - Pregnancy typeType of conception
2  PCI-38Patient clinical information - Pregnancy gestation periodPatient's term of active pregnancy at point of test request.
2  PCI-39Patient clinical information - Fetal gestationStage during patient pregnancy at which it terminated.
2  PCI-40Patient clinical information - Estimated delivery date (EDD)Patient's estimated delivery date.
2  PCI-41Patient clinical information - IVF age of egg donorThe age of the patient who donated the egg at the time of donation.
2  PCI-42Patient clinical information - Had transplantHas the patient ever had a transplant.
2  PCI-43Patient clinical information - Type of transplantWhat type of transplant the patient had.
2  PCI-44Patient clinical information - Transplant dateWhen the patient had the transplant.
2  PCI-45Patient clinical information - Had transfusion in the last 6 weeksHas the patient had a transfusion in the last 6 weeks.
2  PCI-46Patient clinical information - Type of transfusionWhat type of transfusion the patient has had.
2  PCI-47Patient clinical information - Transfusion dateWhen the patient had the transfusion.
2  PCI-48Patient clinical information - Height (m)Patient's height.
1datagroup-miscellaneousMiscellaneousData group - Miscellaneous
2  MIS-1Further supporting informationSupporting information which has not been captured elsewhere.
1datagroup-hospital-encounterHospital encounterData group - Hospital encounter
2  HE-1Treatment function code (TFC)The identifier for the clinical specialty or service under which the patient is being treated.
2  HE-2Hospital provider spell identifierThe identifier for the patient's continuous period of care in a hospital provider setting, from admission to discharge.
2  HE-3Outpatient attendance identifierThe identifier for the patient's specific outpatient appointment at which the genomic test may have been ordered.
2  HE-4Hospital point of delivery codeThe identifier that defines the type of care setting in which the genomic test was requested.

Table View

CodeSystem.id[0]mds-questiontag-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/mds-questiontag-genomics
CodeSystem.version[0]0.1.1
CodeSystem.name[0]MDSQuestionTagGenomics
CodeSystem.title[0]MDS Question Tag Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2025-12-15T00:00:00.000Z
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.description[0]A set of codes used to map MDS Dataset to FHIR Resources.This is intended to be used on Resource.meta.tag.
CodeSystem.copyright[0]Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.hierarchyMeaning[0]grouped-by
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]datagroup-healthcare-professional
CodeSystem.concept[0].display[0]Healthcare Professional
CodeSystem.concept[0].definition[0]Data group - Healthcare professional
CodeSystem.concept[0].concept[0].code[0]HCP-1
CodeSystem.concept[0].concept[0].display[0]HCP - Genomic test order role
CodeSystem.concept[0].concept[0].definition[0]HCP's function within the genomic test ordering process
CodeSystem.concept[0].concept[1].code[0]HCP-2
CodeSystem.concept[0].concept[1].display[0]HCP - First name
CodeSystem.concept[0].concept[1].definition[0]HCP's first name.
CodeSystem.concept[0].concept[2].code[0]HCP-13
CodeSystem.concept[0].concept[2].display[0]HCP - surname
CodeSystem.concept[0].concept[2].definition[0]HCP'surname
CodeSystem.concept[0].concept[3].code[0]HCP-3
CodeSystem.concept[0].concept[3].display[0]HCP - Job title
CodeSystem.concept[0].concept[3].definition[0]HCP's job title.
CodeSystem.concept[0].concept[4].code[0]HCP-4
CodeSystem.concept[0].concept[4].display[0]HCP - Current specialty
CodeSystem.concept[0].concept[4].definition[0]HCP's current specialty.
CodeSystem.concept[0].concept[5].code[0]HCP-5
CodeSystem.concept[0].concept[5].display[0]HCP - Telephone number
CodeSystem.concept[0].concept[5].definition[0]HCP's telephone number.
CodeSystem.concept[0].concept[6].code[0]HCP-6
CodeSystem.concept[0].concept[6].display[0]HCP - Email address
CodeSystem.concept[0].concept[6].definition[0]HCP's email address.
CodeSystem.concept[0].concept[7].code[0]HCP-7
CodeSystem.concept[0].concept[7].display[0]HCP - Organisation name
CodeSystem.concept[0].concept[7].definition[0]HCP's requesting organisation name.
CodeSystem.concept[0].concept[8].code[0]HCP-9
CodeSystem.concept[0].concept[8].display[0]HCP - Organisation ODS code
CodeSystem.concept[0].concept[8].definition[0]HCP's organisation ODS code
CodeSystem.concept[0].concept[9].code[0]HCP-10
CodeSystem.concept[0].concept[9].display[0]HCP - Department name
CodeSystem.concept[0].concept[9].definition[0]HCP's department name.
CodeSystem.concept[0].concept[10].code[0]HCP-11
CodeSystem.concept[0].concept[10].display[0]HCP - Professional registration number
CodeSystem.concept[0].concept[10].definition[0]HCP's professional registration number such as their GMC number.
CodeSystem.concept[0].concept[11].code[0]HCP-12
CodeSystem.concept[0].concept[11].display[0]HCP - Professional registration number type
CodeSystem.concept[0].concept[11].definition[0]HCP's professional registration number type such as 'GMC'.
CodeSystem.concept[1].code[0]datagroup-patient
CodeSystem.concept[1].display[0]Patient
CodeSystem.concept[1].definition[0]Data group - Patient
CodeSystem.concept[1].concept[0].code[0]P-1
CodeSystem.concept[1].concept[0].display[0]Patient - Title
CodeSystem.concept[1].concept[0].definition[0]Patient's title.
CodeSystem.concept[1].concept[1].code[0]P-2
CodeSystem.concept[1].concept[1].display[0]Patient - First name
CodeSystem.concept[1].concept[1].definition[0]Patient's first name.
CodeSystem.concept[1].concept[2].code[0]P-40
CodeSystem.concept[1].concept[2].display[0]Patient - Middlename
CodeSystem.concept[1].concept[2].definition[0]Patient's middle name.
CodeSystem.concept[1].concept[3].code[0]P-3
CodeSystem.concept[1].concept[3].display[0]Patient - Surname
CodeSystem.concept[1].concept[3].definition[0]Patient's last name.
CodeSystem.concept[1].concept[4].code[0]P-41
CodeSystem.concept[1].concept[4].display[0]Patient - Name use
CodeSystem.concept[1].concept[4].definition[0]Links each patient name entry to confirm if current, previous or what the patient is known as.
CodeSystem.concept[1].concept[5].code[0]P-4
CodeSystem.concept[1].concept[5].display[0]Patient - Date of birth
CodeSystem.concept[1].concept[5].definition[0]Patient's date of birth.
CodeSystem.concept[1].concept[6].code[0]P-6
CodeSystem.concept[1].concept[6].display[0]Patient - Postcode
CodeSystem.concept[1].concept[6].definition[0]Patient's home postcode.
CodeSystem.concept[1].concept[7].code[0]P-7
CodeSystem.concept[1].concept[7].display[0]Patient - Country of residence
CodeSystem.concept[1].concept[7].definition[0]Patient's home country.
CodeSystem.concept[1].concept[8].code[0]P-9
CodeSystem.concept[1].concept[8].display[0]Patient - Ethnicity
CodeSystem.concept[1].concept[8].definition[0]Patient's ethnicity.
CodeSystem.concept[1].concept[9].code[0]P-10
CodeSystem.concept[1].concept[9].display[0]Patient - Sex defined at birth
CodeSystem.concept[1].concept[9].definition[0]Patient's phenotypic sex classification as defined at birth based on physical characteristic.
CodeSystem.concept[1].concept[10].code[0]P-12
CodeSystem.concept[1].concept[10].display[0]Patient - GP practice's ODS Code
CodeSystem.concept[1].concept[10].definition[0]Patient's GP practice ODS code.
CodeSystem.concept[1].concept[11].code[0]P-13
CodeSystem.concept[1].concept[11].display[0]Patient - Is from consanguineous union
CodeSystem.concept[1].concept[11].definition[0]The fact of the patient's biological parents being descended from the same ancestor.
CodeSystem.concept[1].concept[12].code[0]P-15
CodeSystem.concept[1].concept[12].display[0]Patient - NHS number
CodeSystem.concept[1].concept[12].definition[0]Patient's NHS number.
CodeSystem.concept[1].concept[13].code[0]P-16
CodeSystem.concept[1].concept[13].display[0]Patient - Local identifier
CodeSystem.concept[1].concept[13].definition[0]Patient's identification code other than NHS number.
CodeSystem.concept[1].concept[14].code[0]P-42
CodeSystem.concept[1].concept[14].display[0]Patient - ODS code of organisation which assigned local identifier
CodeSystem.concept[1].concept[14].definition[0]ODS code of the organisation which assigned the local identifier P-16.
CodeSystem.concept[1].concept[15].code[0]P-17
CodeSystem.concept[1].concept[15].display[0]Patient - Reason for unavailable NHS number
CodeSystem.concept[1].concept[15].definition[0]Reason for an NHS number not being provided.
CodeSystem.concept[1].concept[16].code[0]P-18
CodeSystem.concept[1].concept[16].display[0]Patient - Relationship to proband
CodeSystem.concept[1].concept[16].definition[0]This patient's relationship to the primary patient.
CodeSystem.concept[1].concept[17].code[0]P-19
CodeSystem.concept[1].concept[17].display[0]Patient - Gender Identity
CodeSystem.concept[1].concept[17].definition[0]Patient's stated gender, determined by the patient.
CodeSystem.concept[1].concept[18].code[0]P-20
CodeSystem.concept[1].concept[18].display[0]Patient - Deceased date
CodeSystem.concept[1].concept[18].definition[0]Patient's date of death.
CodeSystem.concept[1].concept[19].code[0]P-21
CodeSystem.concept[1].concept[19].display[0]Patient - Chromosomal sex
CodeSystem.concept[1].concept[19].definition[0]Patient's genomic / karyotypic characteristic. Determined by genomic testing.
CodeSystem.concept[1].concept[20].code[0]P-35
CodeSystem.concept[1].concept[20].display[0]Patient - Withheld identity reason
CodeSystem.concept[1].concept[20].definition[0]Confirmation why the patient is withholding identity details.
CodeSystem.concept[1].concept[21].code[0]P-37
CodeSystem.concept[1].concept[21].display[0]Patient - Local Pedigree / Family identifier
CodeSystem.concept[1].concept[21].definition[0]Patient's pedigree or family identifying id.
CodeSystem.concept[1].concept[22].code[0]P-39
CodeSystem.concept[1].concept[22].display[0]Patient - Reason for inclusion in genomic test request
CodeSystem.concept[1].concept[22].definition[0]Reason patient has been included in genomic test request, such as to support proband testing or providing own genomic reporting
CodeSystem.concept[2].code[0]datagroup-fetus
CodeSystem.concept[2].display[0]Fetus
CodeSystem.concept[2].definition[0]Data group - Fetus
CodeSystem.concept[2].concept[0].code[0]F-1
CodeSystem.concept[2].concept[0].display[0]Fetus - Local identifier
CodeSystem.concept[2].concept[0].definition[0]Fetus' identification code other than NHS number.
CodeSystem.concept[2].concept[1].code[0]F-7
CodeSystem.concept[2].concept[1].display[0]Fetus - ODS code of organisation which assigned local identifier
CodeSystem.concept[2].concept[1].definition[0]ODS code of the organisation which assigned the local identifier F-1.
CodeSystem.concept[2].concept[2].code[0]F-2
CodeSystem.concept[2].concept[2].display[0]Fetus - Observed sex
CodeSystem.concept[2].concept[2].definition[0]Fetus' phenotypic sex classification. Estimated physical characteristic. Currently determined by ultrasound. Gender for PLCM.
CodeSystem.concept[2].concept[3].code[0]F-3
CodeSystem.concept[2].concept[3].display[0]Fetus - Chromosomal sex
CodeSystem.concept[2].concept[3].definition[0]Fetus' genomic / karyotypic characteristic. Determined by genomic testing.
CodeSystem.concept[2].concept[4].code[0]F-6
CodeSystem.concept[2].concept[4].display[0]Fetus - Life status at time of request
CodeSystem.concept[2].concept[4].definition[0]Fetus' alive or deceased status details at the point of test ordering.
CodeSystem.concept[2].concept[5].code[0]F-8
CodeSystem.concept[2].concept[5].display[0]Fetus - Pregnancy id
CodeSystem.concept[2].concept[5].definition[0]The id of a given pregnancy which this fetus belongs to.
CodeSystem.concept[3].code[0]datagroup-test-request
CodeSystem.concept[3].display[0]Test Request
CodeSystem.concept[3].definition[0]Data group - Test Request
CodeSystem.concept[3].concept[0].code[0]TR-2
CodeSystem.concept[3].concept[0].display[0]Test Request - Payment status
CodeSystem.concept[3].concept[0].definition[0]How the test request is funded
CodeSystem.concept[3].concept[1].code[0]TR-4
CodeSystem.concept[3].concept[1].display[0]Test Request - Requesting reason rare disease
CodeSystem.concept[3].concept[1].definition[0]The reason for a rare disease genomic test.
CodeSystem.concept[3].concept[2].code[0]TR-38
CodeSystem.concept[3].concept[2].display[0]Test Request - Requesting reason cancer
CodeSystem.concept[3].concept[2].definition[0]The reason for a cancer genomic test.
CodeSystem.concept[3].concept[3].code[0]TR-5
CodeSystem.concept[3].concept[3].display[0]Test Request - High level test identifier
CodeSystem.concept[3].concept[3].definition[0]Legacy high level ids which identify the requested test. Options provided by old Test Directory.
CodeSystem.concept[3].concept[4].code[0]TR-6
CodeSystem.concept[3].concept[4].display[0]Test Request - High level test identifier description
CodeSystem.concept[3].concept[4].definition[0]Legacy high level name of the id requested
CodeSystem.concept[3].concept[5].code[0]TR-7
CodeSystem.concept[3].concept[5].display[0]Test Request - Low level test identifier
CodeSystem.concept[3].concept[5].definition[0]The low level CITT code which identifies the requested test. Options provided by Test Directory (TEST IDENTIFIER OR TEST CODE).
CodeSystem.concept[3].concept[6].code[0]TR-8
CodeSystem.concept[3].concept[6].display[0]Test Request - Low level test identifier description
CodeSystem.concept[3].concept[6].definition[0]The low level CITT name of the considered test.
CodeSystem.concept[3].concept[7].code[0]TR-9
CodeSystem.concept[3].concept[7].display[0]Test Request - Low level multipurpose test identifier
CodeSystem.concept[3].concept[7].definition[0]The low level code which identifies the test to be actioned when the CITT code is multipurpose (CLINICAL INDICATION).
CodeSystem.concept[3].concept[8].code[0]TR-10
CodeSystem.concept[3].concept[8].display[0]Test Request - Low level multipurpose test identifier description
CodeSystem.concept[3].concept[8].definition[0]The low level name of the test to be actioned when the CITT code is multipurpose.
CodeSystem.concept[3].concept[9].code[0]TR-21
CodeSystem.concept[3].concept[9].display[0]Test Request - Genomic package id
CodeSystem.concept[3].concept[9].definition[0]Id of the package requested.
CodeSystem.concept[3].concept[10].code[0]TR-22
CodeSystem.concept[3].concept[10].display[0]Test Request - Genomic package name
CodeSystem.concept[3].concept[10].definition[0]Name of the package requested.
CodeSystem.concept[3].concept[11].code[0]TR-23
CodeSystem.concept[3].concept[11].display[0]Test Request - Genomic package version
CodeSystem.concept[3].concept[11].definition[0]Version of the package requested.
CodeSystem.concept[3].concept[12].code[0]TR-24
CodeSystem.concept[3].concept[12].display[0]Test Request - Genomic test id
CodeSystem.concept[3].concept[12].definition[0]Id of the test requested.
CodeSystem.concept[3].concept[13].code[0]TR-25
CodeSystem.concept[3].concept[13].display[0]Test Request - Genomic test name
CodeSystem.concept[3].concept[13].definition[0]Name of the test requested.
CodeSystem.concept[3].concept[14].code[0]TR-26
CodeSystem.concept[3].concept[14].display[0]Test Request - Genomic test version
CodeSystem.concept[3].concept[14].definition[0]Version of the test requested.
CodeSystem.concept[3].concept[15].code[0]TR-27
CodeSystem.concept[3].concept[15].display[0]Test Request - Additional panels
CodeSystem.concept[3].concept[15].definition[0]Additional panels to test.
CodeSystem.concept[3].concept[16].code[0]TR-28
CodeSystem.concept[3].concept[16].display[0]Test request - Target type
CodeSystem.concept[3].concept[16].definition[0]Type of target to test.
CodeSystem.concept[3].concept[17].code[0]TR-29
CodeSystem.concept[3].concept[17].display[0]Test request - Target detail
CodeSystem.concept[3].concept[17].definition[0]Detail of target to test.
CodeSystem.concept[3].concept[18].code[0]TR-11
CodeSystem.concept[3].concept[18].display[0]Test Request - Count of patients to be tested
CodeSystem.concept[3].concept[18].definition[0]Count of patients to be tested including the proband/primary patient.
CodeSystem.concept[3].concept[19].code[0]TR-12
CodeSystem.concept[3].concept[19].display[0]Test Request - Urgency reason
CodeSystem.concept[3].concept[19].definition[0]The test request urgency reason.
CodeSystem.concept[3].concept[20].code[0]TR-13
CodeSystem.concept[3].concept[20].display[0]Test Request - Reanalysis reason
CodeSystem.concept[3].concept[20].definition[0]The reason reanalysis has been requested.
CodeSystem.concept[3].concept[21].code[0]TR-14
CodeSystem.concept[3].concept[21].display[0]Test Request - Detail of reason for request
CodeSystem.concept[3].concept[21].definition[0]Further detail associated to the reason reanalysis has been requested.
CodeSystem.concept[3].concept[22].code[0]TR-15
CodeSystem.concept[3].concept[22].display[0]Test Request - Type of reanalysis
CodeSystem.concept[3].concept[22].definition[0]The type of reanalysis which has been requested.
CodeSystem.concept[3].concept[23].code[0]TR-17
CodeSystem.concept[3].concept[23].display[0]Test Request - Is urgent
CodeSystem.concept[3].concept[23].definition[0]Confirmation if the test request is urgent.
CodeSystem.concept[3].concept[24].code[0]TR-35
CodeSystem.concept[3].concept[24].display[0]Test Request - Purpose of linking
CodeSystem.concept[3].concept[24].definition[0]The reason a given test request has been linked to another test request.
CodeSystem.concept[3].concept[25].code[0]TR-36
CodeSystem.concept[3].concept[25].display[0]Test Request - Central email address for reporting
CodeSystem.concept[3].concept[25].definition[0]Central email address for contingency in the event of not being able to obtain a report via the requester.
CodeSystem.concept[3].concept[26].code[0]TR-20
CodeSystem.concept[3].concept[26].display[0]Test Request - Genomic report delivery method
CodeSystem.concept[3].concept[26].definition[0]Test Request - Genomic report delivery method
CodeSystem.concept[3].concept[27].code[0]TR-30
CodeSystem.concept[3].concept[27].display[0]Test Request - Add private genomic request and report to NHS record
CodeSystem.concept[3].concept[27].definition[0]Confirmation if the content of a private genomic test request should be added to an NHS record.
CodeSystem.concept[3].concept[28].code[0]TR-31
CodeSystem.concept[3].concept[28].display[0]Test Request - Test request form version
CodeSystem.concept[3].concept[28].definition[0]Version of the test order form completed and submitted.
CodeSystem.concept[3].concept[29].code[0]TR-32
CodeSystem.concept[3].concept[29].display[0]Test Request - File / Link to file
CodeSystem.concept[3].concept[29].definition[0]Upload of a file or a link to a file for adding documents such as previous genomic reports to a test order.
CodeSystem.concept[3].concept[30].code[0]TR-33
CodeSystem.concept[3].concept[30].display[0]Test Request - File detail
CodeSystem.concept[3].concept[30].definition[0]Detail to provide context to an uploaded file or document link.
CodeSystem.concept[3].concept[31].code[0]TR-34
CodeSystem.concept[3].concept[31].display[0]Test Request - Clinical utility
CodeSystem.concept[3].concept[31].definition[0]Clinical benefit to patient of obtaining a requested genomic report.
CodeSystem.concept[3].concept[32].code[0]TR-39
CodeSystem.concept[3].concept[32].display[0]Test Request - Linked test request reference
CodeSystem.concept[3].concept[32].definition[0]The reference to any associated test requests
CodeSystem.concept[4].code[0]datagroup-ngrl-consent
CodeSystem.concept[4].display[0]NGRL-consent
CodeSystem.concept[4].definition[0]Data group - NGRL consent
CodeSystem.concept[4].concept[0].code[0]NGRL-1
CodeSystem.concept[4].concept[0].display[0]NGRL consent - Date of NGRL consent
CodeSystem.concept[4].concept[0].definition[0]The date NGRL consent was provided.
CodeSystem.concept[4].concept[1].code[0]NGRL-2
CodeSystem.concept[4].concept[1].display[0]NGRL consent - Patient has made their own choice to consent to the NGRL
CodeSystem.concept[4].concept[1].definition[0]Confirmation if the patient to be tested has provided NGRL consent themselves.
CodeSystem.concept[4].concept[2].code[0]NGRL-3
CodeSystem.concept[4].concept[2].display[0]NGRL consent - Patient representative name (if patient cannot make their own choice)
CodeSystem.concept[4].concept[2].definition[0]The name of the patient representative.
CodeSystem.concept[4].concept[3].code[0]NGRL-4
CodeSystem.concept[4].concept[3].display[0]NGRL consent - I confirm that the patient (or their representative) agree to have their genomic and healthcare data used for research
CodeSystem.concept[4].concept[3].definition[0]The outcome of the patient or their representative’s choice in consenting to including their data used for research in the NGRL.
CodeSystem.concept[4].concept[4].code[0]NGRL-5
CodeSystem.concept[4].concept[4].display[0]NGRL consent - NGRL consent document link
CodeSystem.concept[4].concept[4].definition[0]A URL where a copy of a completed NGRL consent form may be found.
CodeSystem.concept[5].code[0]datagroup-primary-sample
CodeSystem.concept[5].display[0]Primary Sample
CodeSystem.concept[5].definition[0]Data group - Primary Sample
CodeSystem.concept[5].concept[0].code[0]PS-2
CodeSystem.concept[5].concept[0].display[0]Primary Sample - Local identifier
CodeSystem.concept[5].concept[0].definition[0]Local ids applied to a sample
CodeSystem.concept[5].concept[1].code[0]PS-3
CodeSystem.concept[5].concept[1].display[0]Primary Sample - ODS code of organisation which assigned local id
CodeSystem.concept[5].concept[1].definition[0]ODS code of the organisation which assigned the local sample id.
CodeSystem.concept[5].concept[2].code[0]PS-10
CodeSystem.concept[5].concept[2].display[0]Primary Sample - Obtained date
CodeSystem.concept[5].concept[2].definition[0]Date at which a specimen/biopsy was obtained from patient.
CodeSystem.concept[5].concept[3].code[0]PS-11
CodeSystem.concept[5].concept[3].display[0]Primary Sample - Primary sample
CodeSystem.concept[5].concept[3].definition[0]The primary sample material.
CodeSystem.concept[5].concept[4].code[0]PS-12
CodeSystem.concept[5].concept[4].display[0]Primary Sample - Primary sample state
CodeSystem.concept[5].concept[4].definition[0]The state of the primary sample.
CodeSystem.concept[5].concept[5].code[0]PS-25
CodeSystem.concept[5].concept[5].display[0]Primary Sample - Preservative/Container
CodeSystem.concept[5].concept[5].definition[0]How the primary sample is preserved.
CodeSystem.concept[5].concept[6].code[0]PS-30
CodeSystem.concept[5].concept[6].display[0]Primary Sample - Block identifier
CodeSystem.concept[5].concept[6].definition[0]Sample block identifier
CodeSystem.concept[5].concept[7].code[0]PS-31
CodeSystem.concept[5].concept[7].display[0]Primary Sample - Fixative type
CodeSystem.concept[5].concept[7].definition[0]Sample fixative type
CodeSystem.concept[5].concept[8].code[0]PS-32
CodeSystem.concept[5].concept[8].display[0]Primary Sample - Hours to fixation
CodeSystem.concept[5].concept[8].definition[0]Sample hours to fixation
CodeSystem.concept[5].concept[9].code[0]PS-33
CodeSystem.concept[5].concept[9].display[0]Primary Sample - Hours in fixative
CodeSystem.concept[5].concept[9].definition[0]Sample hours in fixative
CodeSystem.concept[5].concept[10].code[0]PS-34
CodeSystem.concept[5].concept[10].display[0]Primary Sample - Tumour enrichment method
CodeSystem.concept[5].concept[10].definition[0]Method used for tumour enrichment.
CodeSystem.concept[5].concept[11].code[0]PS-13
CodeSystem.concept[5].concept[11].display[0]Primary Sample - Necrosis
CodeSystem.concept[5].concept[11].definition[0]% necrotic (dead) cells in primary sample.
CodeSystem.concept[5].concept[12].code[0]PS-14
CodeSystem.concept[5].concept[12].display[0]Primary Sample - Nucleated cell count
CodeSystem.concept[5].concept[12].definition[0]Nucleated (with nucleous) cell (non tumour and tumour) count in the primary sample (Solid Tumour and Haem-Onc).
CodeSystem.concept[5].concept[13].code[0]PS-15
CodeSystem.concept[5].concept[13].display[0]Primary Sample - Tumour nuclear content in whole section
CodeSystem.concept[5].concept[13].definition[0]Neoplastic (tumour) cell content in the primary sample whole section(Solid Tumour) - sourced at local lab. (%)
CodeSystem.concept[5].concept[14].code[0]PS-26
CodeSystem.concept[5].concept[14].display[0]Primary Sample - Tumour nuclear content in marked area
CodeSystem.concept[5].concept[14].definition[0]Neoplastic (tumour) cell content in the primary sample marked area(Solid Tumour) - sourced at local lab. (%)
CodeSystem.concept[5].concept[15].code[0]PS-17
CodeSystem.concept[5].concept[15].display[0]Primary Sample - Solid tumour morphology
CodeSystem.concept[5].concept[15].definition[0]The histology and likely course of development of a tumour.
CodeSystem.concept[5].concept[16].code[0]PS-18
CodeSystem.concept[5].concept[16].display[0]Primary Sample - Solid tumour topography
CodeSystem.concept[5].concept[16].definition[0]The tumour sample site. e.g. from colon, stomach etc.
CodeSystem.concept[5].concept[17].code[0]PS-29
CodeSystem.concept[5].concept[17].display[0]Primary Sample - Is biopsy
CodeSystem.concept[5].concept[17].definition[0]Primary Sample - Is biopsy
CodeSystem.concept[5].concept[18].code[0]PS-19
CodeSystem.concept[5].concept[18].display[0]Primary Sample - Biopsy site
CodeSystem.concept[5].concept[18].definition[0]Digital confirmation that the sample is a biopsy.
CodeSystem.concept[5].concept[19].code[0]PS-21
CodeSystem.concept[5].concept[19].display[0]Primary Sample - Observed maternal cell contamination (MCC)
CodeSystem.concept[5].concept[19].definition[0]An observed outcome which may indicate MCC
CodeSystem.concept[5].concept[20].code[0]PS-27
CodeSystem.concept[5].concept[20].display[0]Primary Sample - Test confirmed maternal cell contamination (MCC)
CodeSystem.concept[5].concept[20].definition[0]Analytically confirmed MCC levels
CodeSystem.concept[5].concept[21].code[0]PS-22
CodeSystem.concept[5].concept[21].display[0]Primary Sample - Option for all products of conception
CodeSystem.concept[5].concept[21].definition[0]Primary Sample - Option for all products of conception
CodeSystem.concept[5].concept[22].code[0]PS-23
CodeSystem.concept[5].concept[22].display[0]Primary Sample - Blasts %
CodeSystem.concept[5].concept[22].definition[0]Future management for products of conception.
CodeSystem.concept[5].concept[23].code[0]PS-24
CodeSystem.concept[5].concept[23].display[0]Primary Sample - High infection risk reason
CodeSystem.concept[5].concept[23].definition[0]The high contamination risk reason for a primary sample.
CodeSystem.concept[5].concept[24].code[0]PS-28
CodeSystem.concept[5].concept[24].display[0]Primary Sample - Patient life status at the time of collection
CodeSystem.concept[5].concept[24].definition[0]If the patient was alive or deceased at the point of collecting a sample.
CodeSystem.concept[5].concept[25].code[0]PS-35
CodeSystem.concept[5].concept[25].display[0]Primary Sample - Solid tumour type
CodeSystem.concept[5].concept[25].definition[0]The origin or context of a tumour sample.
CodeSystem.concept[6].code[0]datagroup-patient-clinical-information
CodeSystem.concept[6].display[0]Patient Clinical Information
CodeSystem.concept[6].definition[0]Data group - Patient Clinical Information
CodeSystem.concept[6].concept[0].code[0]PCI-1
CodeSystem.concept[6].concept[0].display[0]Patient clinical information - Genomic Ethnicity
CodeSystem.concept[6].concept[0].definition[0]Patient's ethnicity where 'Patient - Ethnicity field' doesn't provide an adequate description. E.g Ashkenazi Jewish
CodeSystem.concept[6].concept[1].code[0]PCI-2
CodeSystem.concept[6].concept[1].display[0]Patient clinical information - Disease Status
CodeSystem.concept[6].concept[1].definition[0]If the patient is affected, unaffected, or it is unknown.
CodeSystem.concept[6].concept[2].code[0]PCI-4
CodeSystem.concept[6].concept[2].display[0]Patient clinical information - Age at disease onset
CodeSystem.concept[6].concept[2].definition[0]The age when a change in patients' health was first noted in line with suspected diagnosis.
CodeSystem.concept[6].concept[3].code[0]PCI-5
CodeSystem.concept[6].concept[3].display[0]Patient clinical information - Known/Suspected Disease
CodeSystem.concept[6].concept[3].definition[0]Disease a patient is believed, known to have, or be at risk of developing.
CodeSystem.concept[6].concept[4].code[0]PCI-6
CodeSystem.concept[6].concept[4].display[0]Patient clinical information - Phenotypic details
CodeSystem.concept[6].concept[4].definition[0]The HPO (or alternative ontology as appropriate) term names for the observable disease traits.
CodeSystem.concept[6].concept[5].code[0]PCI-7
CodeSystem.concept[6].concept[5].display[0]Patient clinical information - Symptoms
CodeSystem.concept[6].concept[5].definition[0]The patient's symptoms
CodeSystem.concept[6].concept[6].code[0]PCI-10
CodeSystem.concept[6].concept[6].display[0]Patient clinical information - Count of tumours
CodeSystem.concept[6].concept[6].definition[0]How many tumours the patient has.
CodeSystem.concept[6].concept[7].code[0]PCI-11
CodeSystem.concept[6].concept[7].display[0]Patient clinical information - Site of tumour
CodeSystem.concept[6].concept[7].definition[0]Location of the tumours on the body.
CodeSystem.concept[6].concept[8].code[0]PCI-14
CodeSystem.concept[6].concept[8].display[0]Patient clinical information - Tumour sites - Body image diagram
CodeSystem.concept[6].concept[8].definition[0]Image attachment of body with tumour sites highlighted.
CodeSystem.concept[6].concept[9].code[0]PCI-15
CodeSystem.concept[6].concept[9].display[0]Patient clinical information - Pedigree details / Relevant family history
CodeSystem.concept[6].concept[9].definition[0]The patient's pedigree/family history details (inc family history of cancer).
CodeSystem.concept[6].concept[10].code[0]PCI-16
CodeSystem.concept[6].concept[10].display[0]Patient clinical information - Pedigree diagram
CodeSystem.concept[6].concept[10].definition[0]Image attachment of pedigree details
CodeSystem.concept[6].concept[11].code[0]PCI-17
CodeSystem.concept[6].concept[11].display[0]Patient clinical information - Laterality of hearing loss
CodeSystem.concept[6].concept[11].definition[0]Laterality of the hearing loss i.e. bilateral or unilateral.
CodeSystem.concept[6].concept[12].code[0]PCI-18
CodeSystem.concept[6].concept[12].display[0]Patient clinical information - Fetal haemoglobinopathy maternal screening genotype
CodeSystem.concept[6].concept[12].definition[0]Maternal screening genotype for haemoglobinopathy testing.
CodeSystem.concept[6].concept[13].code[0]PCI-21
CodeSystem.concept[6].concept[13].display[0]Patient clinical information - Legal considerations
CodeSystem.concept[6].concept[13].definition[0]Legal considerations for a given request.
CodeSystem.concept[6].concept[14].code[0]PCI-22
CodeSystem.concept[6].concept[14].display[0]Patient clinical information - Fetal haemoglobinopathy paternal screening genotype
CodeSystem.concept[6].concept[14].definition[0]Paternal screening genotype for haemoglobinopathy testing
CodeSystem.concept[6].concept[15].code[0]PCI-23
CodeSystem.concept[6].concept[15].display[0]Patient clinical information - Expected Maternity Unit - Organisation name
CodeSystem.concept[6].concept[15].definition[0]Requesting clinician's organisation name.
CodeSystem.concept[6].concept[16].code[0]PCI-24
CodeSystem.concept[6].concept[16].display[0]Patient clinical information - Expected Maternity Unit - Organisation address
CodeSystem.concept[6].concept[16].definition[0]Requesting clinician's organisation address.
CodeSystem.concept[6].concept[17].code[0]PCI-25
CodeSystem.concept[6].concept[17].display[0]Patient clinical information - Expected Maternity Unit - Organisation ODS code
CodeSystem.concept[6].concept[17].definition[0]Requesting clinician's organisation ODS code.
CodeSystem.concept[6].concept[18].code[0]PCI-26
CodeSystem.concept[6].concept[18].display[0]Patient clinical information - Expected Maternity Unit - Department name
CodeSystem.concept[6].concept[18].definition[0]Requesting clinician's department name.
CodeSystem.concept[6].concept[19].code[0]PCI-27
CodeSystem.concept[6].concept[19].display[0]Patient clinical information - Growth history
CodeSystem.concept[6].concept[19].definition[0]Summary passage of text to highlight patient centile history e.g. head circumference, weight, etc.
CodeSystem.concept[6].concept[20].code[0]PCI-28
CodeSystem.concept[6].concept[20].display[0]Patient clinical information - Severity of hearing loss
CodeSystem.concept[6].concept[20].definition[0]Free text regarding hearing loss
CodeSystem.concept[6].concept[21].code[0]PCI-29
CodeSystem.concept[6].concept[21].display[0]Patient clinical information - Retinal degeneration
CodeSystem.concept[6].concept[21].definition[0]Free text regarding retinal degeneration
CodeSystem.concept[6].concept[22].code[0]PCI-30
CodeSystem.concept[6].concept[22].display[0]Patient clinical information - Risk factors
CodeSystem.concept[6].concept[22].definition[0]Toxic medication - Prematurity (risk factor for hearing loss) e.g. Baby early birth - Ototoxic medication.
CodeSystem.concept[6].concept[23].code[0]PCI-31
CodeSystem.concept[6].concept[23].display[0]Patient clinical information - Suspected inborn error type(s)
CodeSystem.concept[6].concept[23].definition[0]Suspected inborn error type(s)
CodeSystem.concept[6].concept[24].code[0]PCI-32
CodeSystem.concept[6].concept[24].display[0]Patient clinical information - Abnormal infection history site
CodeSystem.concept[6].concept[24].definition[0]Abnormal infection history site organism
CodeSystem.concept[6].concept[25].code[0]PCI-33
CodeSystem.concept[6].concept[25].display[0]Patient clinical information - Abnormal infection history site organism
CodeSystem.concept[6].concept[25].definition[0]Abnormal infection history site organism
CodeSystem.concept[6].concept[26].code[0]PCI-34
CodeSystem.concept[6].concept[26].display[0]Is on ig replacement
CodeSystem.concept[6].concept[26].definition[0]If the patient is on immunoglobin replacement treatment.
CodeSystem.concept[6].concept[27].code[0]PCI-35
CodeSystem.concept[6].concept[27].display[0]Patient clinical information - Current and previous treatment detail
CodeSystem.concept[6].concept[27].definition[0]Detail regarding relevant current and previous medical treatments.
CodeSystem.concept[6].concept[28].code[0]PCI-36
CodeSystem.concept[6].concept[28].display[0]Patient clinical information - Pregnancy status
CodeSystem.concept[6].concept[28].definition[0]Patient`s pregnancy status
CodeSystem.concept[6].concept[29].code[0]PCI-37
CodeSystem.concept[6].concept[29].display[0]Patient clinical information - Pregnancy type
CodeSystem.concept[6].concept[29].definition[0]Type of conception
CodeSystem.concept[6].concept[30].code[0]PCI-38
CodeSystem.concept[6].concept[30].display[0]Patient clinical information - Pregnancy gestation period
CodeSystem.concept[6].concept[30].definition[0]Patient's term of active pregnancy at point of test request.
CodeSystem.concept[6].concept[31].code[0]PCI-39
CodeSystem.concept[6].concept[31].display[0]Patient clinical information - Fetal gestation
CodeSystem.concept[6].concept[31].definition[0]Stage during patient pregnancy at which it terminated.
CodeSystem.concept[6].concept[32].code[0]PCI-40
CodeSystem.concept[6].concept[32].display[0]Patient clinical information - Estimated delivery date (EDD)
CodeSystem.concept[6].concept[32].definition[0]Patient's estimated delivery date.
CodeSystem.concept[6].concept[33].code[0]PCI-41
CodeSystem.concept[6].concept[33].display[0]Patient clinical information - IVF age of egg donor
CodeSystem.concept[6].concept[33].definition[0]The age of the patient who donated the egg at the time of donation.
CodeSystem.concept[6].concept[34].code[0]PCI-42
CodeSystem.concept[6].concept[34].display[0]Patient clinical information - Had transplant
CodeSystem.concept[6].concept[34].definition[0]Has the patient ever had a transplant.
CodeSystem.concept[6].concept[35].code[0]PCI-43
CodeSystem.concept[6].concept[35].display[0]Patient clinical information - Type of transplant
CodeSystem.concept[6].concept[35].definition[0]What type of transplant the patient had.
CodeSystem.concept[6].concept[36].code[0]PCI-44
CodeSystem.concept[6].concept[36].display[0]Patient clinical information - Transplant date
CodeSystem.concept[6].concept[36].definition[0]When the patient had the transplant.
CodeSystem.concept[6].concept[37].code[0]PCI-45
CodeSystem.concept[6].concept[37].display[0]Patient clinical information - Had transfusion in the last 6 weeks
CodeSystem.concept[6].concept[37].definition[0]Has the patient had a transfusion in the last 6 weeks.
CodeSystem.concept[6].concept[38].code[0]PCI-46
CodeSystem.concept[6].concept[38].display[0]Patient clinical information - Type of transfusion
CodeSystem.concept[6].concept[38].definition[0]What type of transfusion the patient has had.
CodeSystem.concept[6].concept[39].code[0]PCI-47
CodeSystem.concept[6].concept[39].display[0]Patient clinical information - Transfusion date
CodeSystem.concept[6].concept[39].definition[0]When the patient had the transfusion.
CodeSystem.concept[6].concept[40].code[0]PCI-48
CodeSystem.concept[6].concept[40].display[0]Patient clinical information - Height (m)
CodeSystem.concept[6].concept[40].definition[0]Patient's height.
CodeSystem.concept[7].code[0]datagroup-miscellaneous
CodeSystem.concept[7].display[0]Miscellaneous
CodeSystem.concept[7].definition[0]Data group - Miscellaneous
CodeSystem.concept[7].concept[0].code[0]MIS-1
CodeSystem.concept[7].concept[0].display[0]Further supporting information
CodeSystem.concept[7].concept[0].definition[0]Supporting information which has not been captured elsewhere.
CodeSystem.concept[8].code[0]datagroup-hospital-encounter
CodeSystem.concept[8].display[0]Hospital encounter
CodeSystem.concept[8].definition[0]Data group - Hospital encounter
CodeSystem.concept[8].concept[0].code[0]HE-1
CodeSystem.concept[8].concept[0].display[0]Treatment function code (TFC)
CodeSystem.concept[8].concept[0].definition[0]The identifier for the clinical specialty or service under which the patient is being treated.
CodeSystem.concept[8].concept[1].code[0]HE-2
CodeSystem.concept[8].concept[1].display[0]Hospital provider spell identifier
CodeSystem.concept[8].concept[1].definition[0]The identifier for the patient's continuous period of care in a hospital provider setting, from admission to discharge.
CodeSystem.concept[8].concept[2].code[0]HE-3
CodeSystem.concept[8].concept[2].display[0]Outpatient attendance identifier
CodeSystem.concept[8].concept[2].definition[0]The identifier for the patient's specific outpatient appointment at which the genomic test may have been ordered.
CodeSystem.concept[8].concept[3].code[0]HE-4
CodeSystem.concept[8].concept[3].display[0]Hospital point of delivery code
CodeSystem.concept[8].concept[3].definition[0]The identifier that defines the type of care setting in which the genomic test was requested.

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="mds-questiontag-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/mds-questiontag-genomics" />
<version value="0.1.1" />
<name value="MDSQuestionTagGenomics" />
<title value="MDS Question Tag Genomics" />
<status value="draft" />
<date value="2025-12-15T00:00:00.000Z" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
</telecom>
</contact>
<description value="A set of codes used to map MDS Dataset to FHIR Resources.This is intended to be used on Resource.meta.tag." />
<copyright value="Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<hierarchyMeaning value="grouped-by" />
<content value="complete" />
<code value="datagroup-healthcare-professional" />
<display value="Healthcare Professional" />
<definition value="Data group - Healthcare professional" />
<code value="HCP-1" />
<display value="HCP - Genomic test order role" />
<definition value="HCP's function within the genomic test ordering process" />
</concept>
<code value="HCP-2" />
<display value="HCP - First name" />
<definition value="HCP's first name." />
</concept>
<code value="HCP-13" />
<display value="HCP - surname" />
<definition value="HCP'surname " />
</concept>
<code value="HCP-3" />
<display value="HCP - Job title" />
<definition value="HCP's job title." />
</concept>
<code value="HCP-4" />
<display value="HCP - Current specialty" />
<definition value="HCP's current specialty." />
</concept>
<code value="HCP-5" />
<display value="HCP - Telephone number" />
<definition value="HCP's telephone number." />
</concept>
<code value="HCP-6" />
<display value="HCP - Email address" />
<definition value="HCP's email address." />
</concept>
<code value="HCP-7" />
<display value="HCP - Organisation name" />
<definition value="HCP's requesting organisation name." />
</concept>
<code value="HCP-9" />
<display value="HCP - Organisation ODS code" />
<definition value="HCP's organisation ODS code" />
</concept>
<code value="HCP-10" />
<display value="HCP - Department name" />
<definition value="HCP's department name." />
</concept>
<code value="HCP-11" />
<display value="HCP - Professional registration number" />
<definition value="HCP's professional registration number such as their GMC number." />
</concept>
<code value="HCP-12" />
<display value="HCP - Professional registration number type" />
<definition value="HCP's professional registration number type such as 'GMC'." />
</concept>
</concept>
<code value="datagroup-patient" />
<display value="Patient" />
<definition value="Data group - Patient" />
<code value="P-1" />
<display value="Patient - Title" />
<definition value="Patient's title." />
</concept>
<code value="P-2" />
<display value="Patient - First name" />
<definition value="Patient's first name." />
</concept>
<code value="P-40" />
<display value="Patient - Middlename" />
<definition value="Patient's middle name." />
</concept>
<code value="P-3" />
<display value="Patient - Surname" />
<definition value="Patient's last name." />
</concept>
<code value="P-41" />
<display value="Patient - Name use" />
<definition value="Links each patient name entry to confirm if current, previous or what the patient is known as." />
</concept>
<code value="P-4" />
<display value="Patient - Date of birth" />
<definition value="Patient's date of birth." />
</concept>
<code value="P-6" />
<display value="Patient - Postcode" />
<definition value="Patient's home postcode." />
</concept>
<code value="P-7" />
<display value="Patient - Country of residence" />
<definition value="Patient's home country." />
</concept>
<code value="P-9" />
<display value="Patient - Ethnicity" />
<definition value="Patient's ethnicity." />
</concept>
<code value="P-10" />
<display value="Patient - Sex defined at birth" />
<definition value="Patient's phenotypic sex classification as defined at birth based on physical characteristic." />
</concept>
<code value="P-12" />
<display value="Patient - GP practice's ODS Code" />
<definition value="Patient's GP practice ODS code." />
</concept>
<code value="P-13" />
<display value="Patient - Is from consanguineous union" />
<definition value="The fact of the patient's biological parents being descended from the same ancestor." />
</concept>
<code value="P-15" />
<display value="Patient - NHS number" />
<definition value="Patient's NHS number." />
</concept>
<code value="P-16" />
<display value="Patient - Local identifier" />
<definition value="Patient's identification code other than NHS number." />
</concept>
<code value="P-42" />
<display value="Patient - ODS code of organisation which assigned local identifier" />
<definition value="ODS code of the organisation which assigned the local identifier P-16." />
</concept>
<code value="P-17" />
<display value="Patient - Reason for unavailable NHS number" />
<definition value="Reason for an NHS number not being provided." />
</concept>
<code value="P-18" />
<display value="Patient - Relationship to proband" />
<definition value="This patient's relationship to the primary patient." />
</concept>
<code value="P-19" />
<display value="Patient - Gender Identity" />
<definition value="Patient's stated gender, determined by the patient." />
</concept>
<code value="P-20" />
<display value="Patient - Deceased date" />
<definition value="Patient's date of death." />
</concept>
<code value="P-21" />
<display value="Patient - Chromosomal sex" />
<definition value="Patient's genomic / karyotypic characteristic. Determined by genomic testing." />
</concept>
<code value="P-35" />
<display value="Patient - Withheld identity reason" />
<definition value="Confirmation why the patient is withholding identity details." />
</concept>
<code value="P-37" />
<display value="Patient - Local Pedigree / Family identifier" />
<definition value="Patient's pedigree or family identifying id." />
</concept>
<code value="P-39" />
<display value="Patient - Reason for inclusion in genomic test request" />
<definition value="Reason patient has been included in genomic test request, such as to support proband testing or providing own genomic reporting" />
</concept>
</concept>
<code value="datagroup-fetus" />
<display value="Fetus" />
<definition value="Data group - Fetus" />
<code value="F-1" />
<display value="Fetus - Local identifier" />
<definition value="Fetus' identification code other than NHS number." />
</concept>
<code value="F-7" />
<display value="Fetus - ODS code of organisation which assigned local identifier" />
<definition value="ODS code of the organisation which assigned the local identifier F-1." />
</concept>
<code value="F-2" />
<display value="Fetus - Observed sex" />
<definition value="Fetus' phenotypic sex classification. Estimated physical characteristic. Currently determined by ultrasound. Gender for PLCM." />
</concept>
<code value="F-3" />
<display value="Fetus - Chromosomal sex" />
<definition value="Fetus' genomic / karyotypic characteristic. Determined by genomic testing." />
</concept>
<code value="F-6" />
<display value="Fetus - Life status at time of request" />
<definition value="Fetus' alive or deceased status details at the point of test ordering." />
</concept>
<code value="F-8" />
<display value="Fetus - Pregnancy id" />
<definition value="The id of a given pregnancy which this fetus belongs to." />
</concept>
</concept>
<code value="datagroup-test-request" />
<display value="Test Request" />
<definition value="Data group - Test Request" />
<code value="TR-2" />
<display value="Test Request - Payment status" />
<definition value="How the test request is funded" />
</concept>
<code value="TR-4" />
<display value="Test Request - Requesting reason rare disease" />
<definition value="The reason for a rare disease genomic test." />
</concept>
<code value="TR-38" />
<display value="Test Request - Requesting reason cancer" />
<definition value="The reason for a cancer genomic test." />
</concept>
<code value="TR-5" />
<display value="Test Request - High level test identifier" />
<definition value="Legacy high level ids which identify the requested test. Options provided by old Test Directory." />
</concept>
<code value="TR-6" />
<display value="Test Request - High level test identifier description" />
<definition value="Legacy high level name of the id requested" />
</concept>
<code value="TR-7" />
<display value="Test Request - Low level test identifier" />
<definition value="The low level CITT code which identifies the requested test. Options provided by Test Directory (TEST IDENTIFIER OR TEST CODE)." />
</concept>
<code value="TR-8" />
<display value="Test Request - Low level test identifier description" />
<definition value="The low level CITT name of the considered test." />
</concept>
<code value="TR-9" />
<display value="Test Request - Low level multipurpose test identifier" />
<definition value="The low level code which identifies the test to be actioned when the CITT code is multipurpose (CLINICAL INDICATION)." />
</concept>
<code value="TR-10" />
<display value="Test Request - Low level multipurpose test identifier description" />
<definition value="The low level name of the test to be actioned when the CITT code is multipurpose." />
</concept>
<code value="TR-21" />
<display value="Test Request - Genomic package id" />
<definition value="Id of the package requested." />
</concept>
<code value="TR-22" />
<display value="Test Request - Genomic package name" />
<definition value="Name of the package requested." />
</concept>
<code value="TR-23" />
<display value="Test Request - Genomic package version" />
<definition value="Version of the package requested." />
</concept>
<code value="TR-24" />
<display value="Test Request - Genomic test id" />
<definition value="Id of the test requested." />
</concept>
<code value="TR-25" />
<display value="Test Request - Genomic test name" />
<definition value="Name of the test requested." />
</concept>
<code value="TR-26" />
<display value="Test Request - Genomic test version" />
<definition value="Version of the test requested." />
</concept>
<code value="TR-27" />
<display value="Test Request - Additional panels" />
<definition value="Additional panels to test." />
</concept>
<code value="TR-28" />
<display value="Test request - Target type" />
<definition value="Type of target to test." />
</concept>
<code value="TR-29" />
<display value="Test request - Target detail" />
<definition value="Detail of target to test." />
</concept>
<code value="TR-11" />
<display value="Test Request - Count of patients to be tested" />
<definition value="Count of patients to be tested including the proband/primary patient." />
</concept>
<code value="TR-12" />
<display value="Test Request - Urgency reason" />
<definition value="The test request urgency reason." />
</concept>
<code value="TR-13" />
<display value="Test Request - Reanalysis reason" />
<definition value="The reason reanalysis has been requested." />
</concept>
<code value="TR-14" />
<display value="Test Request - Detail of reason for request" />
<definition value="Further detail associated to the reason reanalysis has been requested." />
</concept>
<code value="TR-15" />
<display value="Test Request - Type of reanalysis" />
<definition value="The type of reanalysis which has been requested." />
</concept>
<code value="TR-17" />
<display value="Test Request - Is urgent" />
<definition value="Confirmation if the test request is urgent." />
</concept>
<code value="TR-35" />
<display value="Test Request - Purpose of linking" />
<definition value="The reason a given test request has been linked to another test request." />
</concept>
<code value="TR-36" />
<display value="Test Request - Central email address for reporting" />
<definition value="Central email address for contingency in the event of not being able to obtain a report via the requester." />
</concept>
<code value="TR-20" />
<display value="Test Request - Genomic report delivery method" />
<definition value="Test Request - Genomic report delivery method" />
</concept>
<code value="TR-30" />
<display value="Test Request - Add private genomic request and report to NHS record" />
<definition value="Confirmation if the content of a private genomic test request should be added to an NHS record." />
</concept>
<code value="TR-31" />
<display value="Test Request - Test request form version" />
<definition value="Version of the test order form completed and submitted." />
</concept>
<code value="TR-32" />
<display value="Test Request - File / Link to file" />
<definition value="Upload of a file or a link to a file for adding documents such as previous genomic reports to a test order." />
</concept>
<code value="TR-33" />
<display value="Test Request - File detail" />
<definition value="Detail to provide context to an uploaded file or document link." />
</concept>
<code value="TR-34" />
<display value="Test Request - Clinical utility" />
<definition value="Clinical benefit to patient of obtaining a requested genomic report." />
</concept>
<code value="TR-39" />
<display value="Test Request - Linked test request reference" />
<definition value="The reference to any associated test requests" />
</concept>
</concept>
<code value="datagroup-ngrl-consent" />
<display value="NGRL-consent" />
<definition value="Data group - NGRL consent" />
<code value="NGRL-1" />
<display value="NGRL consent - Date of NGRL consent" />
<definition value="The date NGRL consent was provided." />
</concept>
<code value="NGRL-2" />
<display value="NGRL consent - Patient has made their own choice to consent to the NGRL" />
<definition value="Confirmation if the patient to be tested has provided NGRL consent themselves." />
</concept>
<code value="NGRL-3" />
<display value="NGRL consent - Patient representative name (if patient cannot make their own choice)" />
<definition value="The name of the patient representative." />
</concept>
<code value="NGRL-4" />
<display value="NGRL consent - I confirm that the patient (or their representative) agree to have their genomic and healthcare data used for research" />
<definition value="The outcome of the patient or their representative’s choice in consenting to including their data used for research in the NGRL." />
</concept>
<code value="NGRL-5" />
<display value="NGRL consent - NGRL consent document link" />
<definition value="A URL where a copy of a completed NGRL consent form may be found." />
</concept>
</concept>
<code value="datagroup-primary-sample" />
<display value="Primary Sample" />
<definition value="Data group - Primary Sample" />
<code value="PS-2" />
<display value="Primary Sample - Local identifier" />
<definition value="Local ids applied to a sample" />
</concept>
<code value="PS-3" />
<display value="Primary Sample - ODS code of organisation which assigned local id" />
<definition value="ODS code of the organisation which assigned the local sample id." />
</concept>
<code value="PS-10" />
<display value="Primary Sample - Obtained date" />
<definition value="Date at which a specimen/biopsy was obtained from patient." />
</concept>
<code value="PS-11" />
<display value="Primary Sample - Primary sample" />
<definition value="The primary sample material." />
</concept>
<code value="PS-12" />
<display value="Primary Sample - Primary sample state" />
<definition value="The state of the primary sample." />
</concept>
<code value="PS-25" />
<display value="Primary Sample - Preservative/Container" />
<definition value="How the primary sample is preserved." />
</concept>
<code value="PS-30" />
<display value="Primary Sample - Block identifier" />
<definition value="Sample block identifier" />
</concept>
<code value="PS-31" />
<display value="Primary Sample - Fixative type" />
<definition value="Sample fixative type" />
</concept>
<code value="PS-32" />
<display value="Primary Sample - Hours to fixation" />
<definition value="Sample hours to fixation" />
</concept>
<code value="PS-33" />
<display value="Primary Sample - Hours in fixative" />
<definition value="Sample hours in fixative" />
</concept>
<code value="PS-34" />
<display value="Primary Sample - Tumour enrichment method" />
<definition value="Method used for tumour enrichment." />
</concept>
<code value="PS-13" />
<display value="Primary Sample - Necrosis" />
<definition value="% necrotic (dead) cells in primary sample." />
</concept>
<code value="PS-14" />
<display value="Primary Sample - Nucleated cell count" />
<definition value="Nucleated (with nucleous) cell (non tumour and tumour) count in the primary sample (Solid Tumour and Haem-Onc)." />
</concept>
<code value="PS-15" />
<display value="Primary Sample - Tumour nuclear content in whole section" />
<definition value="Neoplastic (tumour) cell content in the primary sample whole section(Solid Tumour) - sourced at local lab. (%)" />
</concept>
<code value="PS-26" />
<display value="Primary Sample - Tumour nuclear content in marked area" />
<definition value="Neoplastic (tumour) cell content in the primary sample marked area(Solid Tumour) - sourced at local lab. (%)" />
</concept>
<code value="PS-17" />
<display value="Primary Sample - Solid tumour morphology" />
<definition value="The histology and likely course of development of a tumour." />
</concept>
<code value="PS-18" />
<display value="Primary Sample - Solid tumour topography" />
<definition value="The tumour sample site. e.g. from colon, stomach etc." />
</concept>
<code value="PS-29" />
<display value="Primary Sample - Is biopsy" />
<definition value="Primary Sample - Is biopsy" />
</concept>
<code value="PS-19" />
<display value="Primary Sample - Biopsy site" />
<definition value="Digital confirmation that the sample is a biopsy." />
</concept>
<code value="PS-21" />
<display value="Primary Sample - Observed maternal cell contamination (MCC)" />
<definition value="An observed outcome which may indicate MCC" />
</concept>
<code value="PS-27" />
<display value="Primary Sample - Test confirmed maternal cell contamination (MCC)" />
<definition value="Analytically confirmed MCC levels" />
</concept>
<code value="PS-22" />
<display value="Primary Sample - Option for all products of conception" />
<definition value="Primary Sample - Option for all products of conception" />
</concept>
<code value="PS-23" />
<display value="Primary Sample - Blasts %" />
<definition value="Future management for products of conception." />
</concept>
<code value="PS-24" />
<display value="Primary Sample - High infection risk reason" />
<definition value="The high contamination risk reason for a primary sample." />
</concept>
<code value="PS-28" />
<display value="Primary Sample - Patient life status at the time of collection" />
<definition value="If the patient was alive or deceased at the point of collecting a sample." />
</concept>
<code value="PS-35" />
<display value="Primary Sample - Solid tumour type" />
<definition value="The origin or context of a tumour sample." />
</concept>
</concept>
<code value="datagroup-patient-clinical-information" />
<display value="Patient Clinical Information" />
<definition value="Data group - Patient Clinical Information" />
<code value="PCI-1" />
<display value="Patient clinical information - Genomic Ethnicity" />
<definition value="Patient's ethnicity where 'Patient - Ethnicity field' doesn't provide an adequate description. E.g Ashkenazi Jewish" />
</concept>
<code value="PCI-2" />
<display value="Patient clinical information - Disease Status" />
<definition value="If the patient is affected, unaffected, or it is unknown." />
</concept>
<code value="PCI-4" />
<display value="Patient clinical information - Age at disease onset" />
<definition value="The age when a change in patients' health was first noted in line with suspected diagnosis." />
</concept>
<code value="PCI-5" />
<display value="Patient clinical information - Known/Suspected Disease" />
<definition value="Disease a patient is believed, known to have, or be at risk of developing." />
</concept>
<code value="PCI-6" />
<display value="Patient clinical information - Phenotypic details" />
<definition value="The HPO (or alternative ontology as appropriate) term names for the observable disease traits." />
</concept>
<code value="PCI-7" />
<display value="Patient clinical information - Symptoms" />
<definition value="The patient's symptoms" />
</concept>
<code value="PCI-10" />
<display value="Patient clinical information - Count of tumours" />
<definition value="How many tumours the patient has." />
</concept>
<code value="PCI-11" />
<display value="Patient clinical information - Site of tumour" />
<definition value="Location of the tumours on the body." />
</concept>
<code value="PCI-14" />
<display value="Patient clinical information - Tumour sites - Body image diagram" />
<definition value="Image attachment of body with tumour sites highlighted." />
</concept>
<code value="PCI-15" />
<display value="Patient clinical information - Pedigree details / Relevant family history" />
<definition value="The patient's pedigree/family history details (inc family history of cancer)." />
</concept>
<code value="PCI-16" />
<display value="Patient clinical information - Pedigree diagram" />
<definition value="Image attachment of pedigree details" />
</concept>
<code value="PCI-17" />
<display value="Patient clinical information - Laterality of hearing loss" />
<definition value="Laterality of the hearing loss i.e. bilateral or unilateral." />
</concept>
<code value="PCI-18" />
<display value="Patient clinical information - Fetal haemoglobinopathy maternal screening genotype" />
<definition value="Maternal screening genotype for haemoglobinopathy testing." />
</concept>
<code value="PCI-21" />
<display value="Patient clinical information - Legal considerations" />
<definition value="Legal considerations for a given request." />
</concept>
<code value="PCI-22" />
<display value="Patient clinical information - Fetal haemoglobinopathy paternal screening genotype" />
<definition value="Paternal screening genotype for haemoglobinopathy testing" />
</concept>
<code value="PCI-23" />
<display value="Patient clinical information - Expected Maternity Unit - Organisation name" />
<definition value="Requesting clinician's organisation name." />
</concept>
<code value="PCI-24" />
<display value="Patient clinical information - Expected Maternity Unit - Organisation address" />
<definition value="Requesting clinician's organisation address." />
</concept>
<code value="PCI-25" />
<display value="Patient clinical information - Expected Maternity Unit - Organisation ODS code" />
<definition value="Requesting clinician's organisation ODS code." />
</concept>
<code value="PCI-26" />
<display value="Patient clinical information - Expected Maternity Unit - Department name" />
<definition value="Requesting clinician's department name." />
</concept>
<code value="PCI-27" />
<display value="Patient clinical information - Growth history" />
<definition value="Summary passage of text to highlight patient centile history e.g. head circumference, weight, etc." />
</concept>
<code value="PCI-28" />
<display value="Patient clinical information - Severity of hearing loss" />
<definition value="Free text regarding hearing loss" />
</concept>
<code value="PCI-29" />
<display value="Patient clinical information - Retinal degeneration" />
<definition value="Free text regarding retinal degeneration" />
</concept>
<code value="PCI-30" />
<display value="Patient clinical information - Risk factors" />
<definition value="Toxic medication - Prematurity (risk factor for hearing loss) e.g. Baby early birth - Ototoxic medication." />
</concept>
<code value="PCI-31" />
<display value="Patient clinical information - Suspected inborn error type(s)" />
<definition value="Suspected inborn error type(s)" />
</concept>
<code value="PCI-32" />
<display value="Patient clinical information - Abnormal infection history site" />
<definition value="Abnormal infection history site organism" />
</concept>
<code value="PCI-33" />
<display value="Patient clinical information - Abnormal infection history site organism" />
<definition value="Abnormal infection history site organism" />
</concept>
<code value="PCI-34" />
<display value="Is on ig replacement" />
<definition value="If the patient is on immunoglobin replacement treatment." />
</concept>
<code value="PCI-35" />
<display value="Patient clinical information - Current and previous treatment detail" />
<definition value="Detail regarding relevant current and previous medical treatments." />
</concept>
<code value="PCI-36" />
<display value="Patient clinical information - Pregnancy status" />
<definition value="Patient`s pregnancy status" />
</concept>
<code value="PCI-37" />
<display value="Patient clinical information - Pregnancy type" />
<definition value="Type of conception" />
</concept>
<code value="PCI-38" />
<display value="Patient clinical information - Pregnancy gestation period" />
<definition value="Patient's term of active pregnancy at point of test request." />
</concept>
<code value="PCI-39" />
<display value="Patient clinical information - Fetal gestation" />
<definition value="Stage during patient pregnancy at which it terminated." />
</concept>
<code value="PCI-40" />
<display value="Patient clinical information - Estimated delivery date (EDD)" />
<definition value="Patient's estimated delivery date." />
</concept>
<code value="PCI-41" />
<display value="Patient clinical information - IVF age of egg donor" />
<definition value="The age of the patient who donated the egg at the time of donation." />
</concept>
<code value="PCI-42" />
<display value="Patient clinical information - Had transplant" />
<definition value="Has the patient ever had a transplant." />
</concept>
<code value="PCI-43" />
<display value="Patient clinical information - Type of transplant" />
<definition value="What type of transplant the patient had." />
</concept>
<code value="PCI-44" />
<display value="Patient clinical information - Transplant date" />
<definition value="When the patient had the transplant." />
</concept>
<code value="PCI-45" />
<display value="Patient clinical information - Had transfusion in the last 6 weeks" />
<definition value="Has the patient had a transfusion in the last 6 weeks." />
</concept>
<code value="PCI-46" />
<display value="Patient clinical information - Type of transfusion" />
<definition value="What type of transfusion the patient has had." />
</concept>
<code value="PCI-47" />
<display value="Patient clinical information - Transfusion date" />
<definition value="When the patient had the transfusion." />
</concept>
<code value="PCI-48" />
<display value="Patient clinical information - Height (m)" />
<definition value="Patient's height." />
</concept>
</concept>
<code value="datagroup-miscellaneous" />
<display value="Miscellaneous" />
<definition value="Data group - Miscellaneous" />
<code value="MIS-1" />
<display value="Further supporting information" />
<definition value="Supporting information which has not been captured elsewhere." />
</concept>
</concept>
<code value="datagroup-hospital-encounter" />
<display value="Hospital encounter" />
<definition value="Data group - Hospital encounter" />
<code value="HE-1" />
<display value="Treatment function code (TFC)" />
<definition value="The identifier for the clinical specialty or service under which the patient is being treated." />
</concept>
<code value="HE-2" />
<display value="Hospital provider spell identifier" />
<definition value="The identifier for the patient's continuous period of care in a hospital provider setting, from admission to discharge." />
</concept>
<code value="HE-3" />
<display value="Outpatient attendance identifier" />
<definition value="The identifier for the patient's specific outpatient appointment at which the genomic test may have been ordered." />
</concept>
<code value="HE-4" />
<display value="Hospital point of delivery code" />
<definition value="The identifier that defines the type of care setting in which the genomic test was requested." />
</concept>
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "mds-questiontag-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/mds-questiontag-genomics",
"version": "0.1.1",
"name": "MDSQuestionTagGenomics",
"title": "MDS Question Tag Genomics",
"status": "draft",
"date": "2025-12-15T00:00:00.000Z",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net"
}
]
}
],
"description": "A set of codes used to map MDS Dataset to FHIR Resources.This is intended to be used on Resource.meta.tag.",
"copyright": "Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"hierarchyMeaning": "grouped-by",
"content": "complete",
"concept": [
{
"code": "datagroup-healthcare-professional",
"display": "Healthcare Professional",
"definition": "Data group - Healthcare professional",
"concept": [
{
"code": "HCP-1",
"display": "HCP - Genomic test order role",
"definition": "HCP's function within the genomic test ordering process"
},
{
"code": "HCP-2",
"display": "HCP - First name",
"definition": "HCP's first name."
},
{
"code": "HCP-13",
"display": "HCP - surname",
"definition": "HCP'surname"
},
{
"code": "HCP-3",
"display": "HCP - Job title",
"definition": "HCP's job title."
},
{
"code": "HCP-4",
"display": "HCP - Current specialty",
"definition": "HCP's current specialty."
},
{
"code": "HCP-5",
"display": "HCP - Telephone number",
"definition": "HCP's telephone number."
},
{
"code": "HCP-6",
"display": "HCP - Email address",
"definition": "HCP's email address."
},
{
"code": "HCP-7",
"display": "HCP - Organisation name",
"definition": "HCP's requesting organisation name."
},
{
"code": "HCP-9",
"display": "HCP - Organisation ODS code",
"definition": "HCP's organisation ODS code"
},
{
"code": "HCP-10",
"display": "HCP - Department name",
"definition": "HCP's department name."
},
{
"code": "HCP-11",
"display": "HCP - Professional registration number",
"definition": "HCP's professional registration number such as their GMC number."
},
{
"code": "HCP-12",
"display": "HCP - Professional registration number type",
"definition": "HCP's professional registration number type such as 'GMC'."
}
]
},
{
"code": "datagroup-patient",
"display": "Patient",
"definition": "Data group - Patient",
"concept": [
{
"code": "P-1",
"display": "Patient - Title",
"definition": "Patient's title."
},
{
"code": "P-2",
"display": "Patient - First name",
"definition": "Patient's first name."
},
{
"code": "P-40",
"display": "Patient - Middlename",
"definition": "Patient's middle name."
},
{
"code": "P-3",
"display": "Patient - Surname",
"definition": "Patient's last name."
},
{
"code": "P-41",
"display": "Patient - Name use",
"definition": "Links each patient name entry to confirm if current, previous or what the patient is known as."
},
{
"code": "P-4",
"display": "Patient - Date of birth",
"definition": "Patient's date of birth."
},
{
"code": "P-6",
"display": "Patient - Postcode",
"definition": "Patient's home postcode."
},
{
"code": "P-7",
"display": "Patient - Country of residence",
"definition": "Patient's home country."
},
{
"code": "P-9",
"display": "Patient - Ethnicity",
"definition": "Patient's ethnicity."
},
{
"code": "P-10",
"display": "Patient - Sex defined at birth",
"definition": "Patient's phenotypic sex classification as defined at birth based on physical characteristic."
},
{
"code": "P-12",
"display": "Patient - GP practice's ODS Code",
"definition": "Patient's GP practice ODS code."
},
{
"code": "P-13",
"display": "Patient - Is from consanguineous union",
"definition": "The fact of the patient's biological parents being descended from the same ancestor."
},
{
"code": "P-15",
"display": "Patient - NHS number",
"definition": "Patient's NHS number."
},
{
"code": "P-16",
"display": "Patient - Local identifier",
"definition": "Patient's identification code other than NHS number."
},
{
"code": "P-42",
"display": "Patient - ODS code of organisation which assigned local identifier",
"definition": "ODS code of the organisation which assigned the local identifier P-16."
},
{
"code": "P-17",
"display": "Patient - Reason for unavailable NHS number",
"definition": "Reason for an NHS number not being provided."
},
{
"code": "P-18",
"display": "Patient - Relationship to proband",
"definition": "This patient's relationship to the primary patient."
},
{
"code": "P-19",
"display": "Patient - Gender Identity",
"definition": "Patient's stated gender, determined by the patient."
},
{
"code": "P-20",
"display": "Patient - Deceased date",
"definition": "Patient's date of death."
},
{
"code": "P-21",
"display": "Patient - Chromosomal sex",
"definition": "Patient's genomic / karyotypic characteristic. Determined by genomic testing."
},
{
"code": "P-35",
"display": "Patient - Withheld identity reason",
"definition": "Confirmation why the patient is withholding identity details."
},
{
"code": "P-37",
"display": "Patient - Local Pedigree / Family identifier",
"definition": "Patient's pedigree or family identifying id."
},
{
"code": "P-39",
"display": "Patient - Reason for inclusion in genomic test request",
"definition": "Reason patient has been included in genomic test request, such as to support proband testing or providing own genomic reporting"
}
]
},
{
"code": "datagroup-fetus",
"display": "Fetus",
"definition": "Data group - Fetus",
"concept": [
{
"code": "F-1",
"display": "Fetus - Local identifier",
"definition": "Fetus' identification code other than NHS number."
},
{
"code": "F-7",
"display": "Fetus - ODS code of organisation which assigned local identifier",
"definition": "ODS code of the organisation which assigned the local identifier F-1."
},
{
"code": "F-2",
"display": "Fetus - Observed sex",
"definition": "Fetus' phenotypic sex classification. Estimated physical characteristic. Currently determined by ultrasound. Gender for PLCM."
},
{
"code": "F-3",
"display": "Fetus - Chromosomal sex",
"definition": "Fetus' genomic / karyotypic characteristic. Determined by genomic testing."
},
{
"code": "F-6",
"display": "Fetus - Life status at time of request",
"definition": "Fetus' alive or deceased status details at the point of test ordering."
},
{
"code": "F-8",
"display": "Fetus - Pregnancy id",
"definition": "The id of a given pregnancy which this fetus belongs to."
}
]
},
{
"code": "datagroup-test-request",
"display": "Test Request",
"definition": "Data group - Test Request",
"concept": [
{
"code": "TR-2",
"display": "Test Request - Payment status",
"definition": "How the test request is funded"
},
{
"code": "TR-4",
"display": "Test Request - Requesting reason rare disease",
"definition": "The reason for a rare disease genomic test."
},
{
"code": "TR-38",
"display": "Test Request - Requesting reason cancer",
"definition": "The reason for a cancer genomic test."
},
{
"code": "TR-5",
"display": "Test Request - High level test identifier",
"definition": "Legacy high level ids which identify the requested test. Options provided by old Test Directory."
},
{
"code": "TR-6",
"display": "Test Request - High level test identifier description",
"definition": "Legacy high level name of the id requested"
},
{
"code": "TR-7",
"display": "Test Request - Low level test identifier",
"definition": "The low level CITT code which identifies the requested test. Options provided by Test Directory (TEST IDENTIFIER OR TEST CODE)."
},
{
"code": "TR-8",
"display": "Test Request - Low level test identifier description",
"definition": "The low level CITT name of the considered test."
},
{
"code": "TR-9",
"display": "Test Request - Low level multipurpose test identifier",
"definition": "The low level code which identifies the test to be actioned when the CITT code is multipurpose (CLINICAL INDICATION)."
},
{
"code": "TR-10",
"display": "Test Request - Low level multipurpose test identifier description",
"definition": "The low level name of the test to be actioned when the CITT code is multipurpose."
},
{
"code": "TR-21",
"display": "Test Request - Genomic package id",
"definition": "Id of the package requested."
},
{
"code": "TR-22",
"display": "Test Request - Genomic package name",
"definition": "Name of the package requested."
},
{
"code": "TR-23",
"display": "Test Request - Genomic package version",
"definition": "Version of the package requested."
},
{
"code": "TR-24",
"display": "Test Request - Genomic test id",
"definition": "Id of the test requested."
},
{
"code": "TR-25",
"display": "Test Request - Genomic test name",
"definition": "Name of the test requested."
},
{
"code": "TR-26",
"display": "Test Request - Genomic test version",
"definition": "Version of the test requested."
},
{
"code": "TR-27",
"display": "Test Request - Additional panels",
"definition": "Additional panels to test."
},
{
"code": "TR-28",
"display": "Test request - Target type",
"definition": "Type of target to test."
},
{
"code": "TR-29",
"display": "Test request - Target detail",
"definition": "Detail of target to test."
},
{
"code": "TR-11",
"display": "Test Request - Count of patients to be tested",
"definition": "Count of patients to be tested including the proband/primary patient."
},
{
"code": "TR-12",
"display": "Test Request - Urgency reason",
"definition": "The test request urgency reason."
},
{
"code": "TR-13",
"display": "Test Request - Reanalysis reason",
"definition": "The reason reanalysis has been requested."
},
{
"code": "TR-14",
"display": "Test Request - Detail of reason for request",
"definition": "Further detail associated to the reason reanalysis has been requested."
},
{
"code": "TR-15",
"display": "Test Request - Type of reanalysis",
"definition": "The type of reanalysis which has been requested."
},
{
"code": "TR-17",
"display": "Test Request - Is urgent",
"definition": "Confirmation if the test request is urgent."
},
{
"code": "TR-35",
"display": "Test Request - Purpose of linking",
"definition": "The reason a given test request has been linked to another test request."
},
{
"code": "TR-36",
"display": "Test Request - Central email address for reporting",
"definition": "Central email address for contingency in the event of not being able to obtain a report via the requester."
},
{
"code": "TR-20",
"display": "Test Request - Genomic report delivery method",
"definition": "Test Request - Genomic report delivery method"
},
{
"code": "TR-30",
"display": "Test Request - Add private genomic request and report to NHS record",
"definition": "Confirmation if the content of a private genomic test request should be added to an NHS record."
},
{
"code": "TR-31",
"display": "Test Request - Test request form version",
"definition": "Version of the test order form completed and submitted."
},
{
"code": "TR-32",
"display": "Test Request - File / Link to file",
"definition": "Upload of a file or a link to a file for adding documents such as previous genomic reports to a test order."
},
{
"code": "TR-33",
"display": "Test Request - File detail",
"definition": "Detail to provide context to an uploaded file or document link."
},
{
"code": "TR-34",
"display": "Test Request - Clinical utility",
"definition": "Clinical benefit to patient of obtaining a requested genomic report."
},
{
"code": "TR-39",
"display": "Test Request - Linked test request reference",
"definition": "The reference to any associated test requests"
}
]
},
{
"code": "datagroup-ngrl-consent",
"display": "NGRL-consent",
"definition": "Data group - NGRL consent",
"concept": [
{
"code": "NGRL-1",
"display": "NGRL consent - Date of NGRL consent",
"definition": "The date NGRL consent was provided."
},
{
"code": "NGRL-2",
"display": "NGRL consent - Patient has made their own choice to consent to the NGRL",
"definition": "Confirmation if the patient to be tested has provided NGRL consent themselves."
},
{
"code": "NGRL-3",
"display": "NGRL consent - Patient representative name (if patient cannot make their own choice)",
"definition": "The name of the patient representative."
},
{
"code": "NGRL-4",
"display": "NGRL consent - I confirm that the patient (or their representative) agree to have their genomic and healthcare data used for research",
"definition": "The outcome of the patient or their representative’s choice in consenting to including their data used for research in the NGRL."
},
{
"code": "NGRL-5",
"display": "NGRL consent - NGRL consent document link",
"definition": "A URL where a copy of a completed NGRL consent form may be found."
}
]
},
{
"code": "datagroup-primary-sample",
"display": "Primary Sample",
"definition": "Data group - Primary Sample",
"concept": [
{
"code": "PS-2",
"display": "Primary Sample - Local identifier",
"definition": "Local ids applied to a sample"
},
{
"code": "PS-3",
"display": "Primary Sample - ODS code of organisation which assigned local id",
"definition": "ODS code of the organisation which assigned the local sample id."
},
{
"code": "PS-10",
"display": "Primary Sample - Obtained date",
"definition": "Date at which a specimen/biopsy was obtained from patient."
},
{
"code": "PS-11",
"display": "Primary Sample - Primary sample",
"definition": "The primary sample material."
},
{
"code": "PS-12",
"display": "Primary Sample - Primary sample state",
"definition": "The state of the primary sample."
},
{
"code": "PS-25",
"display": "Primary Sample - Preservative/Container",
"definition": "How the primary sample is preserved."
},
{
"code": "PS-30",
"display": "Primary Sample - Block identifier",
"definition": "Sample block identifier"
},
{
"code": "PS-31",
"display": "Primary Sample - Fixative type",
"definition": "Sample fixative type"
},
{
"code": "PS-32",
"display": "Primary Sample - Hours to fixation",
"definition": "Sample hours to fixation"
},
{
"code": "PS-33",
"display": "Primary Sample - Hours in fixative",
"definition": "Sample hours in fixative"
},
{
"code": "PS-34",
"display": "Primary Sample - Tumour enrichment method",
"definition": "Method used for tumour enrichment."
},
{
"code": "PS-13",
"display": "Primary Sample - Necrosis",
"definition": "% necrotic (dead) cells in primary sample."
},
{
"code": "PS-14",
"display": "Primary Sample - Nucleated cell count",
"definition": "Nucleated (with nucleous) cell (non tumour and tumour) count in the primary sample (Solid Tumour and Haem-Onc)."
},
{
"code": "PS-15",
"display": "Primary Sample - Tumour nuclear content in whole section",
"definition": "Neoplastic (tumour) cell content in the primary sample whole section(Solid Tumour) - sourced at local lab. (%)"
},
{
"code": "PS-26",
"display": "Primary Sample - Tumour nuclear content in marked area",
"definition": "Neoplastic (tumour) cell content in the primary sample marked area(Solid Tumour) - sourced at local lab. (%)"
},
{
"code": "PS-17",
"display": "Primary Sample - Solid tumour morphology",
"definition": "The histology and likely course of development of a tumour."
},
{
"code": "PS-18",
"display": "Primary Sample - Solid tumour topography",
"definition": "The tumour sample site. e.g. from colon, stomach etc."
},
{
"code": "PS-29",
"display": "Primary Sample - Is biopsy",
"definition": "Primary Sample - Is biopsy"
},
{
"code": "PS-19",
"display": "Primary Sample - Biopsy site",
"definition": "Digital confirmation that the sample is a biopsy."
},
{
"code": "PS-21",
"display": "Primary Sample - Observed maternal cell contamination (MCC)",
"definition": "An observed outcome which may indicate MCC"
},
{
"code": "PS-27",
"display": "Primary Sample - Test confirmed maternal cell contamination (MCC)",
"definition": "Analytically confirmed MCC levels"
},
{
"code": "PS-22",
"display": "Primary Sample - Option for all products of conception",
"definition": "Primary Sample - Option for all products of conception"
},
{
"code": "PS-23",
"display": "Primary Sample - Blasts %",
"definition": "Future management for products of conception."
},
{
"code": "PS-24",
"display": "Primary Sample - High infection risk reason",
"definition": "The high contamination risk reason for a primary sample."
},
{
"code": "PS-28",
"display": "Primary Sample - Patient life status at the time of collection",
"definition": "If the patient was alive or deceased at the point of collecting a sample."
},
{
"code": "PS-35",
"display": "Primary Sample - Solid tumour type",
"definition": "The origin or context of a tumour sample."
}
]
},
{
"code": "datagroup-patient-clinical-information",
"display": "Patient Clinical Information",
"definition": "Data group - Patient Clinical Information",
"concept": [
{
"code": "PCI-1",
"display": "Patient clinical information - Genomic Ethnicity",
"definition": "Patient's ethnicity where 'Patient - Ethnicity field' doesn't provide an adequate description. E.g Ashkenazi Jewish"
},
{
"code": "PCI-2",
"display": "Patient clinical information - Disease Status",
"definition": "If the patient is affected, unaffected, or it is unknown."
},
{
"code": "PCI-4",
"display": "Patient clinical information - Age at disease onset",
"definition": "The age when a change in patients' health was first noted in line with suspected diagnosis."
},
{
"code": "PCI-5",
"display": "Patient clinical information - Known/Suspected Disease",
"definition": "Disease a patient is believed, known to have, or be at risk of developing."
},
{
"code": "PCI-6",
"display": "Patient clinical information - Phenotypic details",
"definition": "The HPO (or alternative ontology as appropriate) term names for the observable disease traits."
},
{
"code": "PCI-7",
"display": "Patient clinical information - Symptoms",
"definition": "The patient's symptoms"
},
{
"code": "PCI-10",
"display": "Patient clinical information - Count of tumours",
"definition": "How many tumours the patient has."
},
{
"code": "PCI-11",
"display": "Patient clinical information - Site of tumour",
"definition": "Location of the tumours on the body."
},
{
"code": "PCI-14",
"display": "Patient clinical information - Tumour sites - Body image diagram",
"definition": "Image attachment of body with tumour sites highlighted."
},
{
"code": "PCI-15",
"display": "Patient clinical information - Pedigree details / Relevant family history",
"definition": "The patient's pedigree/family history details (inc family history of cancer)."
},
{
"code": "PCI-16",
"display": "Patient clinical information - Pedigree diagram",
"definition": "Image attachment of pedigree details"
},
{
"code": "PCI-17",
"display": "Patient clinical information - Laterality of hearing loss",
"definition": "Laterality of the hearing loss i.e. bilateral or unilateral."
},
{
"code": "PCI-18",
"display": "Patient clinical information - Fetal haemoglobinopathy maternal screening genotype",
"definition": "Maternal screening genotype for haemoglobinopathy testing."
},
{
"code": "PCI-21",
"display": "Patient clinical information - Legal considerations",
"definition": "Legal considerations for a given request."
},
{
"code": "PCI-22",
"display": "Patient clinical information - Fetal haemoglobinopathy paternal screening genotype",
"definition": "Paternal screening genotype for haemoglobinopathy testing"
},
{
"code": "PCI-23",
"display": "Patient clinical information - Expected Maternity Unit - Organisation name",
"definition": "Requesting clinician's organisation name."
},
{
"code": "PCI-24",
"display": "Patient clinical information - Expected Maternity Unit - Organisation address",
"definition": "Requesting clinician's organisation address."
},
{
"code": "PCI-25",
"display": "Patient clinical information - Expected Maternity Unit - Organisation ODS code",
"definition": "Requesting clinician's organisation ODS code."
},
{
"code": "PCI-26",
"display": "Patient clinical information - Expected Maternity Unit - Department name",
"definition": "Requesting clinician's department name."
},
{
"code": "PCI-27",
"display": "Patient clinical information - Growth history",
"definition": "Summary passage of text to highlight patient centile history e.g. head circumference, weight, etc."
},
{
"code": "PCI-28",
"display": "Patient clinical information - Severity of hearing loss",
"definition": "Free text regarding hearing loss"
},
{
"code": "PCI-29",
"display": "Patient clinical information - Retinal degeneration",
"definition": "Free text regarding retinal degeneration"
},
{
"code": "PCI-30",
"display": "Patient clinical information - Risk factors",
"definition": "Toxic medication - Prematurity (risk factor for hearing loss) e.g. Baby early birth - Ototoxic medication."
},
{
"code": "PCI-31",
"display": "Patient clinical information - Suspected inborn error type(s)",
"definition": "Suspected inborn error type(s)"
},
{
"code": "PCI-32",
"display": "Patient clinical information - Abnormal infection history site",
"definition": "Abnormal infection history site organism"
},
{
"code": "PCI-33",
"display": "Patient clinical information - Abnormal infection history site organism",
"definition": "Abnormal infection history site organism"
},
{
"code": "PCI-34",
"display": "Is on ig replacement",
"definition": "If the patient is on immunoglobin replacement treatment."
},
{
"code": "PCI-35",
"display": "Patient clinical information - Current and previous treatment detail",
"definition": "Detail regarding relevant current and previous medical treatments."
},
{
"code": "PCI-36",
"display": "Patient clinical information - Pregnancy status",
"definition": "Patient`s pregnancy status"
},
{
"code": "PCI-37",
"display": "Patient clinical information - Pregnancy type",
"definition": "Type of conception"
},
{
"code": "PCI-38",
"display": "Patient clinical information - Pregnancy gestation period",
"definition": "Patient's term of active pregnancy at point of test request."
},
{
"code": "PCI-39",
"display": "Patient clinical information - Fetal gestation",
"definition": "Stage during patient pregnancy at which it terminated."
},
{
"code": "PCI-40",
"display": "Patient clinical information - Estimated delivery date (EDD)",
"definition": "Patient's estimated delivery date."
},
{
"code": "PCI-41",
"display": "Patient clinical information - IVF age of egg donor",
"definition": "The age of the patient who donated the egg at the time of donation."
},
{
"code": "PCI-42",
"display": "Patient clinical information - Had transplant",
"definition": "Has the patient ever had a transplant."
},
{
"code": "PCI-43",
"display": "Patient clinical information - Type of transplant",
"definition": "What type of transplant the patient had."
},
{
"code": "PCI-44",
"display": "Patient clinical information - Transplant date",
"definition": "When the patient had the transplant."
},
{
"code": "PCI-45",
"display": "Patient clinical information - Had transfusion in the last 6 weeks",
"definition": "Has the patient had a transfusion in the last 6 weeks."
},
{
"code": "PCI-46",
"display": "Patient clinical information - Type of transfusion",
"definition": "What type of transfusion the patient has had."
},
{
"code": "PCI-47",
"display": "Patient clinical information - Transfusion date",
"definition": "When the patient had the transfusion."
},
{
"code": "PCI-48",
"display": "Patient clinical information - Height (m)",
"definition": "Patient's height."
}
]
},
{
"code": "datagroup-miscellaneous",
"display": "Miscellaneous",
"definition": "Data group - Miscellaneous",
"concept": [
{
"code": "MIS-1",
"display": "Further supporting information",
"definition": "Supporting information which has not been captured elsewhere."
}
]
},
{
"code": "datagroup-hospital-encounter",
"display": "Hospital encounter",
"definition": "Data group - Hospital encounter",
"concept": [
{
"code": "HE-1",
"display": "Treatment function code (TFC)",
"definition": "The identifier for the clinical specialty or service under which the patient is being treated."
},
{
"code": "HE-2",
"display": "Hospital provider spell identifier",
"definition": "The identifier for the patient's continuous period of care in a hospital provider setting, from admission to discharge."
},
{
"code": "HE-3",
"display": "Outpatient attendance identifier",
"definition": "The identifier for the patient's specific outpatient appointment at which the genomic test may have been ordered."
},
{
"code": "HE-4",
"display": "Hospital point of delivery code",
"definition": "The identifier that defines the type of care setting in which the genomic test was requested."
}
]
}
]
}