{
  "id": 11752,
  "label": "hemophilia A with vascular abnormality",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010603",
  "properties": {
    "xrefs": [
      "GARD:0024740",
      "MEDGEN:336105",
      "MESH:C564415",
      "OMIM:306800",
      "UMLS:C1844137"
    ],
    "synonyms": [
      "hemophilia A with vascular abnormality"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "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"
    }
  ]
}