{
  "id": 14874,
  "label": "immunodeficiency, common variable, 7",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013862",
  "properties": {
    "xrefs": [
      "DOID:0081150",
      "GARD:0015836",
      "MEDGEN:762276",
      "NANDO:2200801",
      "OMIM:614699",
      "Orphanet:696894",
      "UMLS:C3542922"
    ],
    "synonyms": [
      "immunodeficiency, common variable, 7",
      "immunodeficiency, common variable, type 7",
      "CVID7"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16333,
      "label": "common variable immunodeficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16974
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12177",
          "GARD:0006140",
          "ICD10CM:D83",
          "ICD10WHO:D83",
          "ICD9:279.06",
          "MEDGEN:40407",
          "MESH:D017074",
          "MedDRA:10021449",
          "NANDO:1200344",
          "NANDO:2200717",
          "NCIT:C26725",
          "NORD:990",
          "OMIMPS:607594",
          "Orphanet:1572",
          "SCTID:23238000",
          "UMLS:C0009447",
          "icd11.foundation:1908371517"
        ],
        "synonyms": [
          "Common Variable Immune Deficiency",
          "idiopathic immunoglobulin deficiency",
          "primary antibody deficiency",
          "primary hypogammaglobulinemia",
          "secondary hypogammaglobulinemia",
          "Immunoglobulin deficiency, late-onset",
          "acquired agammaglobulinemia",
          "acquired hypogammaglobulinemia",
          "common variable hypogamma-globulinemia",
          "common variable immune deficiency",
          "hypogamma-globulinemia, acquired"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Common variable immunodeficiency (CVID) comprises a heterogeneous group of diseases characterized by a significant hypogammaglobulinemia of unknown cause, failure to produce specific antibodies after immunizations and susceptibility to bacterial infections, predominantly caused by encapsulated bacteria."
      },
      "child_count": 16,
      "reference_id": "MONDO:0015517"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16333,
      "label": "common variable immunodeficiency"
    }
  ]
}