{
  "id": 16480,
  "label": "moderately severe hemophilia A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015720",
  "properties": {
    "xrefs": [
      "GARD:0017060",
      "MEDGEN:543974",
      "Orphanet:169805",
      "UMLS:C0272323"
    ],
    "synonyms": [
      "moderately severe factor VIII deficiency",
      "moderately severe haemophilia type A",
      "moderately severe hemophilia type A"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Moderately severe hemophilia A is a form of hemophilia A characterized by factor VIII deficiency leading to 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"
    }
  ]
}