Paget's Disease

PH3623 / 8721

OpenSAFELY

Jan 26, 2026

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OpenCodelists Phenotype
  1. Overview

    Codelist ID
    opensafely/pagets-disease
    Version ID
    1c199d13
    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.

    Identifies codes which refer to Paget's disease of the bone.

    © 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. Methodology

    Search terms / synonyms / search strategy: Paget, Osteitis deformans

    Inclusion criteria for codes: Code indicates patient has Paget's disease of bone

    Exclusion criteria for codes: Code does not indicate patient has Paget's disease of bone. Note that Paget’s disease can refer to two entirely different conditions, depending on the context: Paget's disease of bone, or Paget's disease of skin - this codelist excludes any codes that likely refer to the latter.

  4. References

  5. Clinical Codelist

  6. API

    To Export Phenotype Details:

    FormatAPI
    JSON site_root/api/v1/phenotypes/PH3623/version/8721/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(
     'PH3623',
     version_id=8721
    )

    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(
     'PH3623',
     version_id=8721
    )

    To Export Phenotype Code List:

    FormatAPI
    JSON site_root/api/v1/phenotypes/PH3623/version/8721/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(
     'PH3623',
     version_id=8721
    )

    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(
     'PH3623',
     version_id=8721
    )

  7. Version History

    Version IDNameOwnerPublish date
    Paget's Disease ieuan.scanlon2026-01-26 23:26