{
  "id": 4361,
  "label": "factor VII deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002244",
  "properties": {
    "xrefs": [
      "GARD:0023098",
      "ICD9:286.3",
      "MEDGEN:8769",
      "MESH:D005168",
      "NANDO:2200675",
      "SCTID:37193007",
      "UMLS:C0015503"
    ],
    "synonyms": [
      "F7 deficiency",
      "deficiency, stable",
      "factor 7 deficiency",
      "factor VII deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "A coagulation disorder characterized by the partial or complete absence of factor VII 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": 10454,
      "label": "congenital factor VII deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4361,
        16482
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2215",
          "GARD:0002238",
          "MEDGEN:473015",
          "MedDRA:10016079",
          "NCIT:C131631",
          "OMIM:227500",
          "Orphanet:327",
          "UMLS:C0272320"
        ],
        "synonyms": [
          "congenital factor VII deficiency",
          "congenital proconvertin deficiency",
          "hypoproconvertinemia",
          "F7 deficiency",
          "factor 7 deficiency",
          "factor VII deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009211"
    },
    {
      "id": 22900,
      "label": "acquired factor VII deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4361,
        20034
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022409",
          "MEDGEN:1388639",
          "NCIT:C131625",
          "Orphanet:599495",
          "UMLS:C4331989"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0035738"
    }
  ],
  "roots": [
    {
      "id": 4359,
      "label": "coagulation protein disease"
    },
    {
      "id": 4360,
      "label": "hemorrhagic disease"
    }
  ]
}