{
  "id": 13782,
  "label": "Brugada syndrome 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012742",
  "properties": {
    "xrefs": [
      "DOID:0110220",
      "GARD:0010361",
      "MEDGEN:395633",
      "MESH:C567509",
      "OMIM:611875",
      "UMLS:C2678478"
    ],
    "synonyms": [
      "BRGDA3",
      "Brugada syndrome 3",
      "Brugada syndrome caused by mutation in CACNA1C",
      "Brugada syndrome type 3",
      "CACNA1C Brugada syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Any Brugada syndrome in which the cause of the disease is a mutation in the CACNA1C gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16147,
      "label": "Brugada syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3258,
        4370,
        26601
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050451",
          "GARD:0001030",
          "ICD9:746.89",
          "MEDGEN:222975",
          "MESH:D053840",
          "MedDRA:10059027",
          "NCIT:C142891",
          "NORD:878",
          "OMIMPS:601144",
          "Orphanet:130",
          "SCTID:418818005",
          "UMLS:C1142166",
          "icd11.foundation:1250136584"
        ],
        "synonyms": [
          "Brugada syndrome",
          "Brugada type idiopathic ventricular fibrillation",
          "idiopathic ventricular fibrillation, Brugada type",
          "right bundle branch block, ST segment elevation, and sudden death syndrome",
          "sudden unexplained nocturnal death syndrome",
          "sudden unexpected nocturnal death syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A genetically heterogeneous condition characterized by complete or incomplete right bundle branch block accompanied by ST elevation in leads V1-V3. There is a high incidence of ventricular arrhythmia that may result in sudden death."
      },
      "child_count": 27,
      "reference_id": "MONDO:0015263"
    },
    {
      "id": 24701,
      "label": "CACNA1C-related disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "definition": "Any human disease (syndromic or non syndromic) in which the cause of the disease is a variation in the CACNA1C gene."
      },
      "child_count": 4,
      "reference_id": "MONDO:0700321"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16147,
      "label": "Brugada syndrome"
    },
    {
      "id": 24701,
      "label": "CACNA1C-related disorder"
    }
  ]
}