{
  "id": 17110,
  "label": "familial hypodysfibrinogenemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016638",
  "properties": {
    "xrefs": [
      "GARD:0017202",
      "MEDGEN:347987",
      "Orphanet:248408",
      "UMLS:C1859970"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10010,
      "label": "congenital afibrinogenemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        15452
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2236",
          "GARD:0005761",
          "MEDGEN:749036",
          "MESH:D000347",
          "NANDO:2200672",
          "NCIT:C98130",
          "NORD:739",
          "OMIM:202400",
          "Orphanet:98880",
          "SCTID:154818001",
          "UMLS:C2584774"
        ],
        "synonyms": [
          "factor I deficiency",
          "afibrinogenemia",
          "afibrinogenemia congenital",
          "afibrinogenemia, congenital",
          "familial afibrinogenemia",
          "hypofibrinogenemia, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Familial afibrinogenemia is a coagulation disorder characterized by bleeding symptoms due to a complete absence of circulating fibrinogen."
      },
      "child_count": 2,
      "reference_id": "MONDO:0008737"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10010,
      "label": "congenital afibrinogenemia"
    }
  ]
}