{
  "id": 12486,
  "label": "ventricular fibrillation, paroxysmal familial, type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011376",
  "properties": {
    "xrefs": [
      "GARD:0024795",
      "MEDGEN:414502",
      "MESH:C567851",
      "OMIM:603829",
      "SCTID:233915000",
      "UMLS:C2751898"
    ],
    "synonyms": [
      "VF1",
      "ventricular fibrillation, familial, 1",
      "ventricular fibrillation, paroxysmal familial, 1",
      "ventricular fibrillation, paroxysmal familial, type 1",
      "IVF",
      "ventricular fibrillation during myocardial infarction, susceptibility to"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23974,
      "label": "paroxysmal familial ventricular fibrillation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2763,
        26601
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004227",
          "MEDGEN:83310",
          "Orphanet:228140",
          "UMLS:C0340493"
        ],
        "synonyms": [
          "IVF",
          "idiopathic ventricular fibrillation",
          "idiopathic ventricular fibrillation, non Brugada type",
          "paroxysmal familial ventricular fibrillation",
          "paroxysmal familial ventricular fibrillation (disorder)",
          "paroxysmal ventricular fibrillation",
          "ventricular fibrillation, paroxysmal familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A rare, genetic, cardiac rhythm disease characterized by ventricular fibrillation in the absence of any structural or functional heart disease, or known repolarization abnormalities. The presence of J waves is associated with a higher risk of nocturnal ventricular fibrillation events and a higher risk of recurrence."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100234"
    },
    {
      "id": 26602,
      "label": "SCN5A-related cardiac rhythm disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        26601
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "SCN5A-related cardiac rhythm disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A heterogeneous collection of cardiac rhythm disorders caused by genetic variations in the SCN5A gene with autosomal dominant inheritance. Affected individuals are commonly reported to have unremarkable cardiac morphology and at least one cardiac rhythm phenotype that includes, but is not limited to, atrial fibrillation, sick sinus syndrome, progressive cardiac conduction disease, ventricular fibrillation, long QT syndrome, and Brugada syndrome."
      },
      "child_count": 6,
      "reference_id": "MONDO:1010181"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23974,
      "label": "paroxysmal familial ventricular fibrillation"
    },
    {
      "id": 26602,
      "label": "SCN5A-related cardiac rhythm disorder"
    }
  ]
}