{
  "id": 10455,
  "label": "congenital factor X deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009212",
  "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."
  },
  "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": 16482,
      "label": "congenital vitamin K-dependent coagulation factors deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4359,
        4360,
        10564,
        20411
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112172",
          "GARD:0020121",
          "MEDGEN:1378036",
          "OMIMPS:277450",
          "Orphanet:169826",
          "Orphanet:98434",
          "UMLS:C4510617",
          "icd11.foundation:54644599"
        ],
        "synonyms": [
          "congenital vitamin K-dependent coagulation factors combined deficiency",
          "vitamin K-dependent clotting factors, combined deficiency of"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital vitamin K-dependent coagulation factors deficiency involving multiple coagulation factors."
      },
      "child_count": 20,
      "reference_id": "MONDO:0015722"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4364,
      "label": "factor X deficiency"
    },
    {
      "id": 16482,
      "label": "congenital vitamin K-dependent coagulation factors deficiency"
    }
  ]
}