{
    "disease_id": "DOID:0110645",
    "recommended_name": {
        "id": "DOID:0110645",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110645",
        "name": "long QT syndrome 2",
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110645",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110645",
            "name": "LQT2",
            "description": ""
        },
        {
            "id": "MONDO:0013367",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013367",
            "name": "long QT syndrome 2",
            "description": "An autosomal dominant condition caused by mutation(s) in the KCNH2 gene, encoding potassium voltage-gated channel subfamily H member 2. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death."
        },
        {
            "id": "MONDO:0013367",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013367",
            "name": "LQT2",
            "description": ""
        },
        {
            "id": "MONDO:0013367",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013367",
            "name": "Long QT syndrome, acquired, reduced susceptibility to",
            "description": ""
        },
        {
            "id": "MONDO:0013367",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013367",
            "name": "long QT syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0013367",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013367",
            "name": "long QT syndrome type 2",
            "description": ""
        },
        {
            "id": "MIM:613688",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613688",
            "name": "Long QT syndrome 2",
            "description": "Long QT syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110645"
    ],
    "unlinked_id_list": []
}