{
  "concept_id": 4152,
  "concept_version_id": 11512,
  "coding_system": {
    "id": 4,
    "name": "ICD10 codes",
    "description": "ICD10 Codes"
  },
  "name": "Immunological (ICD-10)",
  "description": null,
  "author": "",
  "entry_date": "2025-01-19",
  "validation_performed": false,
  "validation_description": null,
  "publication_doi": "",
  "publication_link": "",
  "secondary_publication_links": null,
  "paper_published": false,
  "source_reference": "",
  "citation_requirements": null,
  "owner_access": 3,
  "group_access": 1,
  "world_access": 1,
  "tags": null,
  "collections": null,
  "created_by": null,
  "modified_by": null,
  "owner": null,
  "group": null,
  "phenotype_owner": "PH1706",
  "phenotype_owner_history_id": 3631,
  "requested_entity_id": null,
  "components": [
    {
      "id": 9979,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 534795,
          "code": "D71",
          "description": "Functional disorders of polymorphonuclear neutrophils"
        },
        {
          "id": 534796,
          "code": "D72",
          "description": "Other disorders of white blood cells"
        },
        {
          "id": 534797,
          "code": "D720",
          "description": "Genetic anomalies of leukocytes"
        },
        {
          "id": 534798,
          "code": "D728",
          "description": "Other specified disorders of white blood cells"
        },
        {
          "id": 534799,
          "code": "D729",
          "description": "Disorder of white blood cells, unspecified"
        },
        {
          "id": 534800,
          "code": "D800",
          "description": "Hereditary hypogammaglobulinaemia"
        },
        {
          "id": 534801,
          "code": "D801",
          "description": "Nonfamilial hypogammaglobulinaemia"
        },
        {
          "id": 534802,
          "code": "D802",
          "description": "Selective deficiency of immunoglobulin A [IgA]"
        },
        {
          "id": 534803,
          "code": "D803",
          "description": "Selective deficiency of immunoglobulin G [IgG] subclasses"
        },
        {
          "id": 534804,
          "code": "D804",
          "description": "Selective deficiency of immunoglobulin M [IgM]"
        },
        {
          "id": 534805,
          "code": "D805",
          "description": "Immunodeficiency with increased immunoglobulin M"
        },
        {
          "id": 534806,
          "code": "D808",
          "description": "Other immunodeficiencies with predominantly antibody defects"
        },
        {
          "id": 534807,
          "code": "D809",
          "description": "Immunodeficiency with predominantly antibody defects, unspecified"
        },
        {
          "id": 534808,
          "code": "D81",
          "description": "Combined immunodeficiencies"
        },
        {
          "id": 534809,
          "code": "D810",
          "description": "Severe combined immunodeficiency [SCID] with reticular dysgenesis"
        },
        {
          "id": 534810,
          "code": "D811",
          "description": "Severe combined immunodeficiency [SCID] with low T- and B-cell numbers"
        },
        {
          "id": 534811,
          "code": "D812",
          "description": "Severe combined immunodeficiency [SCID] with low or normal B-cell numbers"
        },
        {
          "id": 534812,
          "code": "D813",
          "description": "Adenosine deaminase [ADA] deficiency"
        },
        {
          "id": 534813,
          "code": "D814",
          "description": "Nezelof syndrome"
        },
        {
          "id": 534814,
          "code": "D815",
          "description": "Purine nucleoside phosphorylase [PNP] deficiency"
        },
        {
          "id": 534815,
          "code": "D816",
          "description": "Major histocompatibility complex class I deficiency"
        },
        {
          "id": 534816,
          "code": "D817",
          "description": "Major histocompatibility complex class II deficiency"
        },
        {
          "id": 534817,
          "code": "D818",
          "description": "Other combined immunodeficiencies"
        },
        {
          "id": 534818,
          "code": "D819",
          "description": "Combined immunodeficiency, unspecified"
        },
        {
          "id": 534819,
          "code": "D82",
          "description": "Immunodeficiency associated with other major defects"
        },
        {
          "id": 534820,
          "code": "D820",
          "description": "Wiskott-Aldrich syndrome"
        },
        {
          "id": 534821,
          "code": "D821",
          "description": "Di George syndrome"
        },
        {
          "id": 534822,
          "code": "D822",
          "description": "Immunodeficiency with short-limbed stature"
        },
        {
          "id": 534823,
          "code": "D823",
          "description": "Immunodeficiency following hereditary defective response to Epstein-Barr virus"
        },
        {
          "id": 534824,
          "code": "D824",
          "description": "Hyperimmunoglobulin E [IgE] syndrome"
        },
        {
          "id": 534825,
          "code": "D828",
          "description": "Immunodeficiency associated with other specified major defects"
        },
        {
          "id": 534826,
          "code": "D829",
          "description": "Immunodeficiency associated with major defect, unspecified"
        },
        {
          "id": 534827,
          "code": "D83",
          "description": "Common variable immunodeficiency"
        },
        {
          "id": 534828,
          "code": "D830",
          "description": "Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function"
        },
        {
          "id": 534829,
          "code": "D831",
          "description": "Common variable immunodeficiency with predominant immunoregulatory T-cell disorders"
        },
        {
          "id": 534830,
          "code": "D832",
          "description": "Common variable immunodeficiency with autoantibodies to B- or T-cells"
        },
        {
          "id": 534831,
          "code": "D838",
          "description": "Other common variable immunodeficiencies"
        },
        {
          "id": 534832,
          "code": "D839",
          "description": "Common variable immunodeficiency, unspecified"
        },
        {
          "id": 534833,
          "code": "D84",
          "description": "Other immunodeficiencies"
        },
        {
          "id": 534834,
          "code": "D840",
          "description": "Lymphocyte function antigen-1 [LFA-1] defect"
        },
        {
          "id": 534835,
          "code": "D841",
          "description": "Defects in the complement system"
        },
        {
          "id": 534836,
          "code": "D848",
          "description": "Other specified immunodeficiencies"
        },
        {
          "id": 534837,
          "code": "D849",
          "description": "Immunodeficiency, unspecified"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11512,
      "version_name": "Immunological (ICD-10)",
      "version_date": "2025-01-19T16:22:01.135782Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}