{
  "id": 20023,
  "label": "factor V deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020586",
  "properties": {
    "xrefs": [
      "GARD:0025179",
      "MEDGEN:1369551",
      "MESH:D005166",
      "NANDO:2200674",
      "NCIT:C131738",
      "SCTID:4320005",
      "UMLS:C4317320"
    ],
    "synonyms": [
      "factor V deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "A coagulation disorder characterized by the partial or complete absence of factor V 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"
    }
  ],
  "children": [
    {
      "id": 10453,
      "label": "congenital factor V deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4360,
        20023,
        20411
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2216",
          "GARD:0002237",
          "MEDGEN:4633",
          "MedDRA:10048930",
          "NCIT:C98938",
          "OMIM:227400",
          "Orphanet:326",
          "SCTID:88776002",
          "UMLS:C0015499"
        ],
        "synonyms": [
          "Owren disease",
          "Parahemophilia",
          "Proaccelerin deficiency",
          "congenital factor V deficiency",
          "hereditary Factor V deficiency",
          "hereditary factor V deficiency",
          "labile factor deficiency",
          "Owren Parahemophilia",
          "factor 5 deficiency",
          "factor V deficiency",
          "labile Factor deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital factor V deficiency is an inherited bleeding disorder due to reduced plasma levels of factor V (FV) and characterized by mild to severe bleeding symptoms."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009210"
    },
    {
      "id": 22899,
      "label": "acquired factor V deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20023,
        20034
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022408",
          "MEDGEN:1380582",
          "NCIT:C131624",
          "Orphanet:599490",
          "UMLS:C4329256",
          "icd11.foundation:99894028"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0035737"
    }
  ],
  "roots": [
    {
      "id": 4359,
      "label": "coagulation protein disease"
    }
  ]
}