{
  "id": 9622,
  "label": "thrombophilia due to protein C deficiency, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008316",
  "properties": {
    "xrefs": [
      "DOID:0111909",
      "GARD:0018574",
      "MEDGEN:436138",
      "OMIM:176860",
      "UMLS:C2674321"
    ],
    "synonyms": [
      "thrombophilia 3 due to protein C deficiency, autosomal dominant",
      "thrombophilia due to protein C deficiency, autosomal dominant",
      "Proc deficiency, autosomal dominant",
      "Protein C deficiency, acquired",
      "Protein C deficiency, autosomal dominant",
      "THPH3",
      "thrombophilia due to PROTEIN C deficiency, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19023,
      "label": "hereditary thrombophilia due to congenital protein C deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23980
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3756",
          "GARD:0016544",
          "MEDGEN:671121",
          "MESH:C535424",
          "MESH:D020151",
          "NANDO:1201080",
          "NANDO:2100197",
          "NANDO:2200689",
          "NCIT:C99025",
          "NORD:1899",
          "Orphanet:745",
          "SCTID:76407009",
          "UMLS:C0598221",
          "icd11.foundation:2021932081"
        ],
        "synonyms": [
          "Protein C Deficiency",
          "Protein C deficiency",
          "Protein C deficiency disease",
          "hereditary thrombophilia due to congenital protein C deficiency",
          "protein C deficiency",
          "severe hereditary thrombophilia due to congenital protein C deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital protein C deficiency is an inherited coagulation disorder characterized by deep venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein C."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019145"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19023,
      "label": "hereditary thrombophilia due to congenital protein C deficiency"
    }
  ]
}