{
  "concept_id": 4153,
  "concept_version_id": 11513,
  "coding_system": {
    "id": 5,
    "name": "Read codes v2",
    "description": "Read codes v2"
  },
  "name": "Immunological (Read v2)",
  "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": 9980,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 534854,
          "code": "C390A00",
          "description": "Dysimmunoglobulinaemia NEC"
        },
        {
          "id": 534838,
          "code": "C30yy11",
          "description": "Adenosine-deaminase deficiency"
        },
        {
          "id": 534839,
          "code": "C373C00",
          "description": "AL amyloidosis"
        },
        {
          "id": 534840,
          "code": "C376000",
          "description": "Hereditary angio-oedema"
        },
        {
          "id": 534841,
          "code": "C390.00",
          "description": "Deficiencies of humoral immunity"
        },
        {
          "id": 534842,
          "code": "C390.11",
          "description": "Agammaglobulinaemia"
        },
        {
          "id": 534843,
          "code": "C390000",
          "description": "Hypogammaglobulinaemia NOS"
        },
        {
          "id": 534844,
          "code": "C390100",
          "description": "Selective IgA immunodeficiency"
        },
        {
          "id": 534845,
          "code": "C390200",
          "description": "Selective IgM immunodeficiency"
        },
        {
          "id": 534846,
          "code": "C390300",
          "description": "Selective IgG immunodeficiency"
        },
        {
          "id": 534847,
          "code": "C390500",
          "description": "Congenital hypogammaglobulinaemia"
        },
        {
          "id": 534848,
          "code": "C390511",
          "description": "Bruton's agammaglobulinaemia"
        },
        {
          "id": 534849,
          "code": "C390512",
          "description": "Congenital X-linked agammaglobulinaemia"
        },
        {
          "id": 534850,
          "code": "C390513",
          "description": "Congenital sex-linked agammaglobulinaemia"
        },
        {
          "id": 534851,
          "code": "C390600",
          "description": "Immunodeficiency with IgM hypergammaglobulinaemia"
        },
        {
          "id": 534852,
          "code": "C390700",
          "description": "Common variable immunodeficiency"
        },
        {
          "id": 534853,
          "code": "C390900",
          "description": "Agammaglobulinaemia NEC"
        },
        {
          "id": 534855,
          "code": "C390A11",
          "description": "Dysgammaglobulinaemia NEC"
        },
        {
          "id": 534856,
          "code": "C390C00",
          "description": "Immunoglobulin G4 deficiency"
        },
        {
          "id": 534857,
          "code": "C390C11",
          "description": "IgG4 deficiency"
        },
        {
          "id": 534858,
          "code": "C390y00",
          "description": "Other specified deficiency of humoral immunity"
        },
        {
          "id": 534859,
          "code": "C390z00",
          "description": "Deficiency of humoral immunity NOS"
        },
        {
          "id": 534860,
          "code": "C391100",
          "description": "Di George syndrome"
        },
        {
          "id": 534861,
          "code": "C391200",
          "description": "Wiskott - Aldrich syndrome"
        },
        {
          "id": 534862,
          "code": "C391211",
          "description": "Thrombocytopenic eczema with immunodeficiency"
        },
        {
          "id": 534863,
          "code": "C391300",
          "description": "Nezelof's syndrome"
        },
        {
          "id": 534864,
          "code": "C392.00",
          "description": "Combined immunity deficiency"
        },
        {
          "id": 534865,
          "code": "C392000",
          "description": "Recessive agammaglobulinaemia"
        },
        {
          "id": 534866,
          "code": "C392100",
          "description": "Severe combined immunodeficiency"
        },
        {
          "id": 534867,
          "code": "C392111",
          "description": "Swiss type agammaglobulinaemia"
        },
        {
          "id": 534868,
          "code": "C392200",
          "description": "Thymic aplasia or dysplasia with immunodeficiency"
        },
        {
          "id": 534869,
          "code": "C392300",
          "description": "Severe combined immunodefiency with reticular dysgenesis"
        },
        {
          "id": 534870,
          "code": "C392400",
          "description": "Severe combined immunodeficiency with low T- and B-cell numbers"
        },
        {
          "id": 534871,
          "code": "C392500",
          "description": "Severe combined immunodeficiency with low or normal B-cell numbers"
        },
        {
          "id": 534872,
          "code": "C392600",
          "description": "Adenosine deaminase deficiency"
        },
        {
          "id": 534873,
          "code": "C392700",
          "description": "Purine nucleoside phosphorylase deficiency"
        },
        {
          "id": 534874,
          "code": "C392800",
          "description": "Major histocompatibility complex class I deficiency"
        },
        {
          "id": 534875,
          "code": "C392900",
          "description": "Major histocompatibility complex class II deficiency"
        },
        {
          "id": 534876,
          "code": "C392z00",
          "description": "Combined immunity deficiency NOS"
        },
        {
          "id": 534877,
          "code": "C393.00",
          "description": "Unspecified immunity deficiency"
        },
        {
          "id": 534878,
          "code": "C396.00",
          "description": "Immunodeficiency following hereditary defective response to Epstein-Barr virus"
        },
        {
          "id": 534879,
          "code": "C397.00",
          "description": "Hyperimmunoglobulin E syndrome"
        },
        {
          "id": 534880,
          "code": "C398.00",
          "description": "Common variable immunodeficiency"
        },
        {
          "id": 534881,
          "code": "C398000",
          "description": "Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions"
        },
        {
          "id": 534882,
          "code": "C398100",
          "description": "Common variable immunodeficiency with predominant immunoregulatory T-cell disorders"
        },
        {
          "id": 534883,
          "code": "C398200",
          "description": "Common variable immunodeficiency with autoantibodies to B- or T-cells"
        },
        {
          "id": 534884,
          "code": "C399.00",
          "description": "Defects in the complement system"
        },
        {
          "id": 534885,
          "code": "C399000",
          "description": "Mannose-binding lectin deficiency"
        },
        {
          "id": 534886,
          "code": "C39X.00",
          "description": "Immunodeficiency associated with major defect, unspecified"
        },
        {
          "id": 534887,
          "code": "C39y000",
          "description": "Lymphocyte function antigen-1 defect"
        },
        {
          "id": 534888,
          "code": "Cyu0000",
          "description": "[X]Other immunodeficiencies with predominantly antibody defects"
        },
        {
          "id": 534889,
          "code": "Cyu0100",
          "description": "[X]Other combined immunodeficiency disorders"
        },
        {
          "id": 534890,
          "code": "Cyu0200",
          "description": "[X]Immunodeficiency associated with other specified major defects"
        },
        {
          "id": 534891,
          "code": "Cyu0300",
          "description": "[X]Immunodeficiency associated with major defect, unspecified"
        },
        {
          "id": 534892,
          "code": "Cyu0400",
          "description": "[X]Other common variable immunodeficiencies"
        },
        {
          "id": 534893,
          "code": "Cyu0500",
          "description": "[X]Other specified immunodeficiency disorders"
        },
        {
          "id": 534894,
          "code": "D401.00",
          "description": "Functional disorders of polymorphonuclear neutrophils"
        },
        {
          "id": 534895,
          "code": "D401.11",
          "description": "Job's syndrome"
        },
        {
          "id": 534896,
          "code": "D401000",
          "description": "Congenital dysphagocytosis"
        },
        {
          "id": 534897,
          "code": "D401200",
          "description": "Chronic granulomatous disease"
        },
        {
          "id": 534898,
          "code": "D401z00",
          "description": "Polymorphonuclear neutrophil disorder NOS"
        },
        {
          "id": 534899,
          "code": "D402.00",
          "description": "Genetic leukocyte anomalies"
        },
        {
          "id": 534900,
          "code": "D402.13",
          "description": "Genetic leucocyte anomalies"
        },
        {
          "id": 534901,
          "code": "M15y300",
          "description": "Leiner's disease"
        },
        {
          "id": 534902,
          "code": "PJ3y000",
          "description": "Shprintzen syndrome"
        },
        {
          "id": 534903,
          "code": "PJ3y011",
          "description": "Velocardiofacial syndrome"
        },
        {
          "id": 534904,
          "code": "SN51000",
          "description": "Acquired C1 esterase inhibitor deficiency"
        },
        {
          "id": 534905,
          "code": "SN51100",
          "description": "Hereditary C1 esterase inhibitor deficiency"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11513,
      "version_name": "Immunological (Read v2)",
      "version_date": "2025-01-19T16:22:01.706852Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}