{
  "id": 11581,
  "label": "Bruton-type agammaglobulinemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010421",
  "properties": {
    "xrefs": [
      "DOID:14179",
      "GARD:0001033",
      "MEDGEN:65123",
      "MESH:C537409",
      "MedDRA:10060360",
      "NANDO:1200343",
      "NANDO:2200716",
      "NCIT:C3822",
      "OMIM:300755",
      "Orphanet:47",
      "SCTID:65880007",
      "UMLS:C0221026"
    ],
    "synonyms": [
      "BTK-deficiency",
      "Bruton type agammaglobulinemia",
      "Bruton's Sex-linked agammaglobulinemia",
      "Bruton's X-linked agammaglobulinemia",
      "Bruton-type agammaglobulinemia",
      "X-linked agammaglobulinemia",
      "agammaglobulinemia, X-linked 1, X-linked recessive",
      "Bruton's agammaglobulinemia",
      "XLA",
      "agammaglobulinemia, BTK",
      "agammaglobulinemia, Bruton tyrosine kinase",
      "agammaglobulinemia, X-linked",
      "agammaglobulinemia, X-linked, type 1",
      "hypogammaglobulinemia, X-linked",
      "immunodeficiency 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "X-linked agammaglobulinemia (XLA) is a clinically variable form of isolated agammaglobulinemia, an inherited immunodeficiency disorder, and is characterized in affected males by recurrent bacterial infections during infancy."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16973,
      "label": "isolated agammaglobulinemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16629
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017155",
          "MEDGEN:1639972",
          "Orphanet:229717",
          "SCTID:764858009",
          "UMLS:C4707181"
        ],
        "synonyms": [
          "isolated hypogammaglobulinemia",
          "nonsyndromic agammaglobulinemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Isolated agammaglobulinemia (IA) is the non-syndromic form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy."
      },
      "child_count": 2,
      "reference_id": "MONDO:0016462"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16973,
      "label": "isolated agammaglobulinemia"
    }
  ]
}