{
  "id": 26353,
  "label": "cardiac conduction disease with or without cardiomyoopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0980715",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 8666,
      "label": "cardiac rhythm disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6967
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:427.9",
          "MEDGEN:2039",
          "NCIT:C2881",
          "SCTID:698247007",
          "UMLS:C0003811"
        ],
        "synonyms": [
          "arrhythmia"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any variation from the normal rate or rhythm (which may include the origin of the impulse and/or its subsequent propagation) in the heart."
      },
      "child_count": 17,
      "reference_id": "MONDO:0007263"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6967
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "hereditary heart disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the cardiovascular system."
      },
      "child_count": 146,
      "reference_id": "MONDO:0100547"
    }
  ],
  "children": [
    {
      "id": 24761,
      "label": "cardiac conduction disease with or without dilated cardiomyopathy 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        26353
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIM:616117"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A hereditary atrial tachyarrhythmia-infra-Hisian cardiac conduction disease caused by a variation in the TNNI3K gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0700388"
    },
    {
      "id": 24762,
      "label": "cardiac conduction disease with or without cardiomyopathy 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        26353
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0700389"
    }
  ],
  "roots": [
    {
      "id": 8666,
      "label": "cardiac rhythm disease"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease"
    }
  ]
}