{
  "id": 4364,
  "label": "factor X deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002247",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4359,
      "label": "coagulation protein disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3738
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2212",
          "GARD:0023096",
          "MEDGEN:108723",
          "MESH:D020147",
          "NCIT:C27215",
          "SCTID:86075001",
          "UMLS:C0600503"
        ],
        "synonyms": [
          "coagulation factor deficiency",
          "coagulation factor deficiency syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital or acquired deficiency of one of the coagulation factors. It results in bleeding."
      },
      "child_count": 28,
      "reference_id": "MONDO:0002242"
    },
    {
      "id": 4360,
      "label": "hemorrhagic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7217
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2213",
          "ICD9:287.9",
          "MEDGEN:6799",
          "MESH:D006474",
          "NCIT:C115221",
          "UMLS:C0019087"
        ],
        "synonyms": [
          "bleeding diathesis",
          "bleeding disorder",
          "bleeding predisposition",
          "bleeding tendency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (blood coagulation disorders) or another abnormality causing a structural flaw in the blood vessels (hemostatic disorders)."
      },
      "child_count": 28,
      "reference_id": "MONDO:0002243"
    }
  ],
  "children": [
    {
      "id": 10455,
      "label": "congenital factor X deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4364,
        16482
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2222",
          "GARD:0006404",
          "ICD9:286.3",
          "MEDGEN:543976",
          "NCIT:C98940",
          "OMIM:227600",
          "Orphanet:328",
          "SCTID:37350004",
          "UMLS:C0272327",
          "icd11.foundation:1886781445"
        ],
        "synonyms": [
          "Stuart-Prower factor deficiency",
          "congenital Stuart factor deficiency",
          "congenital factor X deficiency",
          "hereditary Factor X deficiency",
          "F10 deficiency",
          "Stuart factor deficiency, congenital",
          "Stuart-Prower Factor deficiency",
          "factor 10 deficiency",
          "factor X deficiency",
          "factor X deficiency, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009212"
    },
    {
      "id": 20372,
      "label": "acquired factor X deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4364,
        20034
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0021134"
    }
  ],
  "roots": [
    {
      "id": 4359,
      "label": "coagulation protein disease"
    },
    {
      "id": 4360,
      "label": "hemorrhagic disease"
    }
  ]
}