{
  "id": 14405,
  "label": "long QT syndrome 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013372",
  "properties": {
    "xrefs": [
      "DOID:0110647",
      "GARD:0010433",
      "HGNC:6240",
      "MEDGEN:358092",
      "MESH:C566766",
      "NCIT:C172094",
      "OMIM:613695",
      "UMLS:C1867904"
    ],
    "synonyms": [
      "KCNE1 long QT syndrome",
      "LQT5",
      "long QT syndrome 5",
      "long QT syndrome caused by mutation in KCNE1",
      "long QT syndrome type 5",
      "long QT syndrome 2/5, digenic",
      "long QT syndrome 5, acquired, susceptibility to"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Any long QT syndrome in which the cause of the disease is a mutation in the KCNE1 gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 19046,
      "label": "familial long QT syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4527,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016547",
          "MEDGEN:685787",
          "MedDRA:10057926",
          "NANDO:2200228",
          "NORD:1675",
          "OMIMPS:192500",
          "Orphanet:101016",
          "Orphanet:768",
          "SCTID:442917000",
          "UMLS:C1141890",
          "icd11.foundation:1208831985"
        ],
        "synonyms": [
          "LQTS",
          "Long QT Syndrome",
          "Romano-Ward long QT syndrome",
          "Romano-Ward syndrome",
          "Ward-Romano syndrome",
          "congenital long QT syndrome",
          "familial long QT syndrome",
          "hereditary long QT syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias."
      },
      "child_count": 38,
      "reference_id": "MONDO:0019171"
    }
  ],
  "children": [
    {
      "id": 13911,
      "label": "Jervell and Lange-Nielsen syndrome 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4526,
        14405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010364",
          "MEDGEN:394108",
          "MESH:C567343",
          "OMIM:612347",
          "UMLS:C2676723"
        ],
        "synonyms": [
          "Jervell and Lange-Nielsen syndrome 2",
          "Jervell and Lange-Nielsen syndrome caused by mutation in KCNE1",
          "Jervell and Lange-Nielsen syndrome type 2",
          "KCNE1 Jervell and Lange-Nielsen syndrome",
          "JLNS2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Any Jervell and Lange-Nielsen syndrome in which the cause of the disease is a mutation in the KCNE1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012871"
    }
  ],
  "roots": [
    {
      "id": 19046,
      "label": "familial long QT syndrome"
    }
  ]
}