North West Genomic Medicine Service Alliance
0.0.7 - ci-build United Kingdom flag

North West Genomic Medicine Service Alliance - Local Development build (v0.0.7) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

ValueSet: Genomic Rare and Inherited Disease Test Directory

Official URL: https://nw-gmsa.github.io/ValueSet/GenomicRareAndInheritedDisease Version: 0.0.7
Draft as of 2025-08-20 Computable Name: GenomicRareAndInheritedDisease

References

Logical Definition (CLD)

  • Include these codes as defined in https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory
    CodeDisplay
    R14.1Acutely unwell children with a likely monogenic disorder
    R133.1Arrhythmogenic right ventricular cardiomyopathy
    R391.1Barth syndrome
    R128.1Brugada syndrome and cardiac sodium channel disease
    R129.1Catecholaminergic polymorphic VT
    R132.1Dilated and Arrhythmogenic cardiomyopathy
    R140.1Elastin-related phenotypes
    R384.1Generalised arterial calcification in infancy
    R131.1Hypertrophic cardiomyopathy
    R127.1Long QT syndrome
    R135.2Paediatric or syndromic cardiomyopathy
    R135.3Paediatric or syndromic cardiomyopathy
    R136.1Primary lymphoedema
    R328.1Progressive cardiac conduction disease
    R130.1Short QT syndrome
    R138.1Sudden unexplained death or survivors of a cardiac event
    R240.1Diagnostic testing for known variant(s)
    R242.1Predictive testing for known familial variant(s)

 

Expansion

Expansion performed internally based on codesystem Genomic Test Directory v0.0.7 (CodeSystem)

This value set contains 18 concepts

CodeSystemDisplay
  R14.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryAcutely unwell children with a likely monogenic disorder
  R133.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryArrhythmogenic right ventricular cardiomyopathy
  R391.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryBarth syndrome
  R128.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryBrugada syndrome and cardiac sodium channel disease
  R129.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryCatecholaminergic polymorphic VT
  R132.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryDilated and Arrhythmogenic cardiomyopathy
  R140.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryElastin-related phenotypes
  R384.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryGeneralised arterial calcification in infancy
  R131.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryHypertrophic cardiomyopathy
  R127.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryLong QT syndrome
  R135.2https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryPaediatric or syndromic cardiomyopathy
  R135.3https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryPaediatric or syndromic cardiomyopathy
  R136.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryPrimary lymphoedema
  R328.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryProgressive cardiac conduction disease
  R130.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryShort QT syndrome
  R138.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectorySudden unexplained death or survivors of a cardiac event
  R240.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryDiagnostic testing for known variant(s)
  R242.1https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectoryPredictive testing for known familial variant(s)

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code