{
  "id": 16479,
  "label": "severe hemophilia A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015719",
  "properties": {
    "xrefs": [
      "GARD:0017059",
      "MEDGEN:543973",
      "Orphanet:169802",
      "SCTID:16872008",
      "UMLS:C0272322"
    ],
    "synonyms": [
      "severe factor VIII deficiency",
      "severe haemophilia type A",
      "severe hemophilia type A"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Severe hemophilia A is a form of hemophilia A characterized by a large deficiency of factor VIII leading to frequent spontaneous hemorrhage and abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11751,
      "label": "hemophilia A",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2902,
        4360,
        18652,
        20411
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12134",
          "GARD:0006591",
          "ICD10CM:D66",
          "ICD9:286.0",
          "MEDGEN:5501",
          "MESH:D006467",
          "MedDRA:10016080",
          "NANDO:2200676",
          "NCIT:C27146",
          "NORD:1221",
          "OMIM:134500",
          "OMIM:306700",
          "Orphanet:98878",
          "SCTID:234440005",
          "UMLS:C0019069",
          "icd11.foundation:337607970"
        ],
        "synonyms": [
          "congenital factor VIII disorder",
          "factor VIII deficiency",
          "haemophilia a, X-linked recessive",
          "haemophilia type A",
          "haemophilia type a",
          "hemophilia A",
          "hemophilia a, X-linked recessive",
          "hemophilia type A",
          "hemophilia type a",
          "hereditary Factor VIII deficiency",
          "hereditary Factor VIII deficiency disease",
          "HEMA",
          "Haemophilia A",
          "autosomal haemophilia a",
          "autosomal hemophilia a",
          "classic haemophilia",
          "classic hemophilia",
          "classical haemophilia",
          "classical hemophilia",
          "factor 8 deficiency",
          "haemophilia A, congenital",
          "hem A",
          "hemophilia A, congenital",
          "hemophilia, classic"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "The most common form of hemophilia characterized by spontaneous or prolonged hemorrhages due to factor VIII deficiency."
      },
      "child_count": 20,
      "reference_id": "MONDO:0010602"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11751,
      "label": "hemophilia A"
    }
  ]
}