{
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      "namespace_iri": "http://purl.bioontology.org/ontology/SNOMEDCT/",
      "version": "2025AB",
      "title": "Systematized Nomenclature of Medicine – Clinical Terms (SNOMED CT)"
    },
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      "id": "LOINC",
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      "title": "Logical Observation Identifiers Names and Codes (LOINC)"
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      "id": "HP",
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      "version": "2026-02-16",
      "title": "Human Phenotype Ontology (HPO)"
    },
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      "id": "NCIT",
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      "title": "NCI Thesaurus (NCIT) OBO Edition"
    },
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      "id": "HL7FHIR",
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      "title": "Health Level Seven Fast Healthcare Interoperability Resources, Release 4"
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      "title": "Global Alliance for Genomics and Health Phenopackets Schema"
    },
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      "id": "CustomCode",
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      "title": "Custom Code System RD CDM v2.0"
    },
    {
      "id": "NCBITAXON",
      "namespace_iri": "http://purl.obolibrary.org/obo/NCBITAXON/",
      "version": "2025_04_10",
      "title": "NCBI organismal classification"
    },
    {
      "id": "GENO",
      "namespace_iri": "http://purl.obolibrary.org/obo/GENO/",
      "version": "2026-02-02",
      "title": "GENO – The Genotype Ontology"
    },
    {
      "id": "SO",
      "namespace_iri": "http://purl.obolibrary.org/obo/SO/",
      "version": "2.6",
      "title": "Sequence Ontology"
    },
    {
      "id": "UO",
      "namespace_iri": "http://purl.obolibrary.org/obo/UO/",
      "version": "2026-01-16",
      "title": "Units Ontology (UO)"
    },
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      "id": "ECO",
      "namespace_iri": "http://purl.obolibrary.org/obo/ECO/",
      "version": "releases/2025-06-23",
      "title": "Evidence & Conclusion Ontology (ECO)"
    },
    {
      "id": "ICD10CM",
      "namespace_iri": "http://purl.bioontology.org/ontology/ICD10CM/",
      "version": "2026",
      "title": "International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM)"
    },
    {
      "id": "MONDO",
      "namespace_iri": "http://purl.obolibrary.org/obo/MONDO/",
      "version": "2026-03-03",
      "title": "Mondo Disease Ontology"
    },
    {
      "id": "ORDO",
      "namespace_iri": "http://purl.obolibrary.org/obo/ORDO/",
      "version": "4.8",
      "title": "Orphanet Rare Disease Ontology (ORDO)"
    },
    {
      "id": "HGNC",
      "namespace_iri": "http://identifiers.org/hgnc/",
      "version": "2024-08-23",
      "title": "HUGO Gene Nomenclature Committee (HGNC)"
    },
    {
      "id": "OMIM",
      "namespace_iri": "http://purl.bioontology.org/ontology/OMIM/",
      "version": "2025_08_04",
      "title": "Online Mendelian Inheritance in Man (OMIM)"
    },
    {
      "id": "HGVS",
      "namespace_iri": "https://varnomen.hgvs.org/",
      "version": "21.0.0",
      "title": "Human Genome Variation Society Nomenclature"
    },
    {
      "id": "ICD11",
      "namespace_iri": "http://id.who.int/icd/release/11/mms/",
      "version": "2024-09-01",
      "title": "International Classification of Diseases, Eleventh Revision (ICD-11)"
    },
    {
      "id": "ISO3166",
      "namespace_iri": "https://www.iso.org/iso-3166-country-codes.html",
      "version": "2020(en)",
      "title": "International Organization for Standardization – ISO 3166 Country Codes"
    },
    {
      "id": "ICF",
      "namespace_iri": "https://www.who.int/standards/classifications/international-classification-of-functioning-disability-and-health",
      "version": "1.0.2",
      "title": "International Classification of Functioning, Disability and Health (ICF)"
    }
  ],
  "@type": "RdCdm"
}