Rare genetic metabolic and autoimmune disease codes

PH2294 / 5370

NHSD Primary Care Domain Refsets

Jan 26, 2026

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OpenCodelists Phenotype

  1. Overview

    Codelist ID
    nhsd-primary-care-domain-refsets/c19rgmadiag_cod
    Version ID
    7da53558
    Version Tag
    20250912
    Coding System
    SNOMED CT codes
    Collections
    OpenCodelistPhenotype Library
    Tags
    No data

  2. Definition

    This codelist was taken from OpenCodelists, created by OpenSAFELY. We recommend viewing this Phenotype on the OpenCodelist website to view the most recent version.

    Taken from the C19RGMADIAG_COD refset published by NHSD. Contains public sector information licensed under the UK Open Government Licence v3.0 (https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).

    © University of Oxford for the Bennett Institute for Applied Data Science 2025. This work may be copied freely for non-commercial research and study.

  3. References

    Source Reference

    https://www.opencodelists.org/codelist/nhsd-primary-care-domain-refsets/c19rgmadiag_cod/20250912

    References

  4. Clinical Codelist

  5. API

    To Export Phenotype Details:

    FormatAPI
    JSON site_root/api/v1/phenotypes/PH2294/version/5370/detail/?format=json
    R Package

    # Download here

    library(ConceptLibraryClient)


    # Connect to API

    client = ConceptLibraryClient::Connection$new(public=TRUE)


    # Get details of Phenotype

    phenotype_details = client$phenotypes$get_detail(
     'PH2294',
     version_id=5370
    )

    Py Package

    # Download here

    from pyconceptlibraryclient import Client


    # Connect to API

    client = Client(public=True)


    # Get details of Phenotype

    phenotype_detail = client.phenotypes.get_detail(
     'PH2294',
     version_id=5370
    )

    To Export Phenotype Code List:

    FormatAPI
    JSON site_root/api/v1/phenotypes/PH2294/version/5370/export/codes/?format=json
    R Package

    # Download here

    library(ConceptLibraryClient)


    # Connect to API

    client = ConceptLibraryClient::Connection$new(public=TRUE)


    # Get codelist of Phenotype

    phenotype_codelist = client$phenotypes$get_codelist(
     'PH2294',
     version_id=5370
    )

    Py Package

    # Download here

    from pyconceptlibraryclient import Client


    # Connect to API

    client = Client(public=True)


    # Get codelist of Phenotype

    phenotype_codelist = client.phenotypes.get_codelist(
     'PH2294',
     version_id=5370
    )

  6. Version History

    Version IDNameOwnerPublish date
    Rare genetic metabolic and autoimmune disease codes ieuan.scanlon2026-01-26 22:02
    5369 Rare genetic metabolic and autoimmune disease codes ieuan.scanlon2026-01-26 22:02
    5368 Rare genetic metabolic and autoimmune disease codes ieuan.scanlon2026-01-26 22:02
    5367 Rare genetic metabolic and autoimmune disease codes ieuan.scanlon2026-01-26 22:02
    5366 Rare genetic metabolic and autoimmune disease codes ieuan.scanlon2026-01-26 22:02