{
  "id": 25494,
  "label": "short QT syndrome 7",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859368",
  "properties": {
    "xrefs": [
      "GARD:0026720",
      "MEDGEN:1824077",
      "OMIM:620231",
      "UMLS:C5774304"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2916,
      "label": "short QT syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3258,
        26601
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050793",
          "GARD:0016650",
          "ICD9:426.89",
          "MEDGEN:378835",
          "MESH:C580439",
          "NCIT:C71060",
          "NORD:2019",
          "OMIMPS:609620",
          "Orphanet:51083",
          "SCTID:698272007",
          "UMLS:C2348199",
          "icd11.foundation:553392015"
        ],
        "synonyms": [
          "short QT syndrome",
          "ventricular arrhythmia associated with short QT syndrome",
          "familial short QT syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A genetic disease of the electrical system of the heart that consists of a constellation of signs and symptoms, consisting of a short QT interval on an EKG (< 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart. Short QT syndrome appears to be inherited in an autosomal dominant pattern, and a few affected families have been identified"
      },
      "child_count": 8,
      "reference_id": "MONDO:0000453"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2916,
      "label": "short QT syndrome"
    }
  ]
}