{
  "id": 15197,
  "label": "catecholaminergic polymorphic ventricular tachycardia 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014191",
  "properties": {
    "xrefs": [
      "DOID:0060679",
      "GARD:0015967",
      "MEDGEN:815866",
      "OMIM:615441",
      "UMLS:C3809536"
    ],
    "synonyms": [
      "TRDN catecholaminergic polymorphic ventricular tachycardia",
      "cardiac arrhythmia syndrome, with or without skeletal muscle weakness",
      "catecholaminergic polymorphic ventricular tachycardia 5",
      "catecholaminergic polymorphic ventricular tachycardia caused by mutation in TRDN",
      "catecholaminergic polymorphic ventricular tachycardia type 5",
      "CPVT5",
      "ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Any catecholaminergic polymorphic ventricular tachycardia in which the cause of the disease is a mutation in the TRDN gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18166,
      "label": "catecholaminergic polymorphic ventricular tachycardia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3258,
        9929,
        20013
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060674",
          "GARD:0004421",
          "MEDGEN:1803763",
          "MESH:C536334",
          "NANDO:2200216",
          "NANDO:2200221",
          "OMIMPS:604772",
          "Orphanet:3286",
          "SCTID:419671004",
          "UMLS:C5574922",
          "icd11.foundation:976309888"
        ],
        "synonyms": [
          "CPVT",
          "bidirectional tachycardia induced by catecholamine",
          "catecholaminergic polymorphic ventricular tachycardia",
          "double tachycardia induced by catecholamines",
          "malignant paroxysmal ventricular tachycardia",
          "multifocal ventricular premature beats",
          "ventricular tachycardia, catecholaminergic polymorphic",
          "catecholamine-induced polymorphic ventricular tachycardia",
          "familial polymorphic ventricular tachycardia",
          "polymorphic catecholergic ventricular tachycardia",
          "stress-induced polymorphic ventricular tachycardia",
          "syncopal paroxysmal tachycardia"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder characterized by adrenergically induced ventricular tachycardia (VT) manifesting as syncope and sudden death."
      },
      "child_count": 21,
      "reference_id": "MONDO:0017990"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18166,
      "label": "catecholaminergic polymorphic ventricular tachycardia"
    }
  ]
}