{
  "id": 2916,
  "label": "short QT syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000453",
  "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"
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 3258,
      "label": "heart conduction disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6967
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10273",
          "ICD9:426.6",
          "SCTID:44808001"
        ],
        "synonyms": [
          "cardiac conduction disease",
          "cardiac conduction disorder",
          "conduction disease of heart",
          "disease of cardiac conduction",
          "disorder of cardiac conduction"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of the heart's electrical conduction system."
      },
      "child_count": 10,
      "reference_id": "MONDO:0000992"
    },
    {
      "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": 13368,
      "label": "short QT syndrome type 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2916
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018633",
          "MEDGEN:355891",
          "MESH:C566506",
          "OMIM:609620",
          "UMLS:C1865020"
        ],
        "synonyms": [
          "KCNH2 short QT syndrome",
          "SQTS",
          "short QT syndrome caused by mutation in KCNH2",
          "short QT syndrome type 1",
          "SQT1",
          "short QT syndrome 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any short QT syndrome in which the cause of the disease is a mutation in the KCNH2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012312"
    },
    {
      "id": 13369,
      "label": "short QT syndrome type 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2916
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018634",
          "MEDGEN:355890",
          "MESH:C566505",
          "OMIM:609621",
          "UMLS:C1865019"
        ],
        "synonyms": [
          "KCNQ1 short QT syndrome",
          "short QT syndrome caused by mutation in KCNQ1",
          "short QT syndrome type 2",
          "SQT2",
          "short QT syndrome 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any short QT syndrome in which the cause of the disease is a mutation in the KCNQ1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012313"
    },
    {
      "id": 13370,
      "label": "short QT syndrome type 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2916
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018635",
          "MEDGEN:400662",
          "MESH:C566504",
          "OMIM:609622",
          "UMLS:C1865018"
        ],
        "synonyms": [
          "KCNJ2 short QT syndrome",
          "short QT syndrome caused by mutation in KCNJ2",
          "short QT syndrome type 3",
          "SQT3",
          "short QT syndrome 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any short QT syndrome in which the cause of the disease is a mutation in the KCNJ2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012314"
    },
    {
      "id": 25494,
      "label": "short QT syndrome 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2916
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026720",
          "MEDGEN:1824077",
          "OMIM:620231",
          "UMLS:C5774304"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859368"
    }
  ],
  "roots": [
    {
      "id": 3258,
      "label": "heart conduction disease"
    },
    {
      "id": 26601,
      "label": "cardiogenetic rhythm disorder"
    }
  ]
}