{
  "id": 14394,
  "label": "congenital prothrombin deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013361",
  "properties": {
    "xrefs": [
      "DOID:2235",
      "GARD:0002926",
      "ICD9:286.3",
      "MEDGEN:124425",
      "MESH:D007020",
      "NANDO:2200673",
      "NCIT:C131737",
      "OMIM:613679",
      "Orphanet:325",
      "SCTID:73975000",
      "UMLS:C0272317"
    ],
    "synonyms": [
      "factor 2 deficiency",
      "factor II deficiency",
      "hypoprothrombinemia",
      "prothrombin deficiency",
      "Dysprothrombinemia",
      "congenital prothrombin deficiency",
      "hereditary prothrombin deficiency",
      "congenital factor II deficiency",
      "prothrombin deficiency, congenital"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7611,
      "label": "autosomal recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050737",
          "EFO:1000017",
          "ICD9:758.5",
          "MEDGEN:539209",
          "SCTID:85995004",
          "UMLS:C0265388"
        ],
        "synonyms": [
          "autosomal recessive disease or disorder",
          "autosomal recessive hereditary disease",
          "autosomal recessive hereditary disorder",
          "autosomal recessive inherited disease",
          "autosomal recessive inherited disorder",
          "disease or disorder, autosomal recessive",
          "disease, autosomal recessive",
          "recessive hereditary disorder (autosomal)"
        ],
        "definition": "Autosomal recessive form of disease."
      },
      "child_count": 219,
      "reference_id": "MONDO:0006025"
    },
    {
      "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"
    },
    {
      "id": 21340,
      "label": "prothrombin deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025386",
          "MEDGEN:1651913",
          "UMLS:C4722227"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0024307"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 16482,
      "label": "congenital vitamin K-dependent coagulation factors deficiency"
    },
    {
      "id": 21340,
      "label": "prothrombin deficiency"
    }
  ]
}