{
  "id": 9929,
  "label": "ventricular tachycardia, familial",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008648",
  "properties": {
    "xrefs": [
      "GARD:0002263",
      "MEDGEN:83309",
      "OMIM:192605",
      "SCTID:233906007",
      "UMLS:C0340485"
    ],
    "synonyms": [
      "hereditary ventricular tachycardia",
      "ventricular tachycardia, familial",
      "ventricular tachycardia, idiopathic",
      "familial ventricular tachycardia",
      "ventricular tachycardia, familial polymorphic"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "An instance of ventricular tachycardia that is caused by an inherited modification of the individual's genome."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7134,
      "label": "ventricular tachycardia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8666
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005306",
          "ICD10CM:I47.2",
          "MEDGEN:12068",
          "MESH:D017180",
          "NANDO:2100049",
          "NCIT:C50802",
          "SCTID:25569003",
          "UMLS:C0042514",
          "icd11.foundation:1171837620"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disorder characterized by an electrocardiographic finding of three or more consecutive complexes of ventricular origin with a rate greater than a certain threshold (100 or 120 beats per minute are commonly used). The QRS complexes are wide and have an abnormal morphology. (CDISC)"
      },
      "child_count": 3,
      "reference_id": "MONDO:0005477"
    },
    {
      "id": 26601,
      "label": "cardiogenetic rhythm disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8666,
        24272
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "cardiogenetic rhythm disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any cardiac rhythm disorder with a monogenic etiology that includes, but is not limited to, atrial fibrillation, sick sinus syndrome, progressive cardiac conduction disease, ventricular fibrillation, Brugada syndrome, long QT syndrome, short QT syndrome, tachycardia with fibrillation."
      },
      "child_count": 18,
      "reference_id": "MONDO:1010180"
    }
  ],
  "children": [
    {
      "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"
    }
  ],
  "roots": [
    {
      "id": 7134,
      "label": "ventricular tachycardia"
    },
    {
      "id": 26601,
      "label": "cardiogenetic rhythm disorder"
    }
  ]
}