{
  "id": 21340,
  "label": "prothrombin deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024307",
  "properties": {
    "xrefs": [
      "GARD:0025386",
      "MEDGEN:1651913",
      "UMLS:C4722227"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "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": 14394,
      "label": "congenital prothrombin deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7611,
        16482,
        21340
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013361"
    },
    {
      "id": 17402,
      "label": "acquired prothrombin deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21340
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000475",
          "MEDGEN:140275",
          "MESH:C538174",
          "NCIT:C131622",
          "Orphanet:26348",
          "SCTID:4152002",
          "UMLS:C0392610"
        ],
        "synonyms": [
          "acquired hypoprothrombinemia",
          "acquired prothrombin deficiency",
          "acquired factor II deficiency",
          "hypoprothrombinemia, acquired"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An instance of prothrombin deficiency that is acquired during the lifetime of the individual."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016990"
    }
  ],
  "roots": [
    {
      "id": 4360,
      "label": "hemorrhagic disease"
    }
  ]
}