{
  "id": 13911,
  "label": "Jervell and Lange-Nielsen syndrome 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012871",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4526,
      "label": "Jervell and Lange-Nielsen syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19046
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2842",
          "GARD:0003048",
          "MEDGEN:5929",
          "MESH:D029593",
          "MedDRA:10057936",
          "NCIT:C84793",
          "NORD:1310",
          "OMIMPS:220400",
          "Orphanet:90647",
          "SCTID:373905003",
          "UMLS:C0022387"
        ],
        "synonyms": [
          "Jervell Lange-Nielsen syndrome",
          "Jervell and Lange Nielsen syndrome",
          "long QT interval-deafness syndrome",
          "Cardioauditory syndrome of Jervell and Lange-Nielsen",
          "JLNS1",
          "Jervell and Lange-Nielsen syndrome 1",
          "Jervell and Lange-Nielsen syndrome type 1",
          "Surdo-cardiac syndrome",
          "deafness, congenital, and functional heart disease",
          "prolonged QT interval in EKG and sudden death"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "An autosomal recessive inherited syndrome caused by mutations in the KCNE1 and KCNQ1 genes. It is characterized by congenital hearing loss and arrhythmia. It is a form of long QT syndrome."
      },
      "child_count": 2,
      "reference_id": "MONDO:0002441"
    },
    {
      "id": 14405,
      "label": "long QT syndrome 5",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19046
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 1,
      "reference_id": "MONDO:0013372"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4526,
      "label": "Jervell and Lange-Nielsen syndrome"
    },
    {
      "id": 14405,
      "label": "long QT syndrome 5"
    }
  ]
}