{
  "id": 20372,
  "label": "acquired factor X deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0021134",
  "properties": {
    "xrefs": [
      "GARD:0022410",
      "ICD9:286.9",
      "MEDGEN:543977",
      "NANDO:1201048",
      "NCIT:C131626",
      "Orphanet:599501",
      "SCTID:33820001",
      "UMLS:C0272328"
    ],
    "synonyms": [
      "aFX",
      "acquired factor X deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "An bleeding disorder with a decreased antigen and/or activity of factor X (FX) that is acquired. Acquired factor X deficiency is a rare disorder, commonly associated with a preceding viral illness and a circulating FX inhibitor. Although multiple treatment modalities have been described with variable success, in many cases, it is a self-limited condition."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4364,
      "label": "factor X deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4359,
        4360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0023100",
          "MEDGEN:4635",
          "MESH:D005171",
          "NANDO:2200678",
          "NCIT:C131632",
          "SCTID:76642003",
          "UMLS:C0015519"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A coagulation disorder characterized by the partial or complete absence of factor X activity in the blood."
      },
      "child_count": 4,
      "reference_id": "MONDO:0002247"
    },
    {
      "id": 20034,
      "label": "acquired coagulation factor deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4359
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025183",
          "ICD10CM:D68.4",
          "MEDGEN:98",
          "NANDO:1200896",
          "NCIT:C34347",
          "SCTID:25904003",
          "UMLS:C0001169"
        ],
        "synonyms": [
          "acquired coagulation factor deficiency",
          "acquired coagulation protein disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Deficiency of a coagulation factor that is not caused by genetic alterations. Causes include vitamin K deficiency, amyloidosis, and severe liver disease."
      },
      "child_count": 6,
      "reference_id": "MONDO:0020599"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4364,
      "label": "factor X deficiency"
    },
    {
      "id": 20034,
      "label": "acquired coagulation factor deficiency"
    }
  ]
}