{
  "id": 24762,
  "label": "cardiac conduction disease with or without cardiomyopathy 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0700389",
  "properties": {
    "xrefs": [
      "OMIM:621367"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "A hereditary atrial tachyarrhythmia-infra-Hisian cardiac conduction disease caused by a variation in the POPDC2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 26353,
      "label": "cardiac conduction disease with or without cardiomyoopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8666,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIMPS:616117",
          "Orphanet:436242"
        ],
        "synonyms": [
          "hereditary atrial tachyarrhythmia-infra-Hisian cardiac conduction disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A rare genetic cardiac disease characterized by variably expressed atrial tachyarrhythmia (such as atrial flutter, paroxysmal or chronic atrial fibrillation, ectopic atrial tachycardia, or multifocal atrial tachycardia), infra-Hisian conduction system disease, and vulnerability to dilated cardiomyopathy. Age of onset ranges between childhood and adulthood."
      },
      "child_count": 4,
      "reference_id": "MONDO:0980715"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 26353,
      "label": "cardiac conduction disease with or without cardiomyoopathy"
    }
  ]
}