{
  "id": 10010,
  "label": "congenital afibrinogenemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008737",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 15452,
      "label": "familial dysfibrinogenemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18223
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002004",
          "ICD9:286.3",
          "MEDGEN:82901",
          "NCIT:C131659",
          "OMIM:616004",
          "Orphanet:98881",
          "SCTID:111589005",
          "UMLS:C0272350"
        ],
        "synonyms": [
          "dysfibrinogenemia",
          "familial dysfibrinogenemia",
          "hypodysfibrinogenemia",
          "congenital dysfibrinogenemia",
          "dysfibrinogenemia, congenital",
          "dysfibrinogenemia, familial",
          "hypodysfibrinogenemia, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen."
      },
      "child_count": 1,
      "reference_id": "MONDO:0014452"
    }
  ],
  "children": [
    {
      "id": 16062,
      "label": "familial hypofibrinogenemia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10010
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002887",
          "MEDGEN:1826143",
          "Orphanet:101041",
          "UMLS:C5681803"
        ],
        "synonyms": [
          "hypofibrinogenemia, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Familial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015096"
    },
    {
      "id": 17110,
      "label": "familial hypodysfibrinogenemia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10010
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017202",
          "MEDGEN:347987",
          "Orphanet:248408",
          "UMLS:C1859970"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0016638"
    }
  ],
  "roots": [
    {
      "id": 15452,
      "label": "familial dysfibrinogenemia"
    }
  ]
}