{
    "disease_id": "DOID:0110644",
    "recommended_name": {
        "id": "DOID:0110644",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110644",
        "name": "long QT syndrome 1",
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4."
    },
    "synonyms": [
        {
            "id": "DOID:0110644",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110644",
            "name": "LQT1",
            "description": ""
        },
        {
            "id": "DOID:0110644",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110644",
            "name": "ventricular fibrillation with prolonged QT interval",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "long QT syndrome 1",
            "description": "Romano-Ward syndrome (RWS) is an autosomal dominant variant of the long QT syndrome (LQTS, see this term) characterized by syncopal episodes and electrocardiographic abnormalities (QT prolongation, T-wave abnormalities and torsade de pointes (TdP) ventricular tachycardia)."
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "Romano-Ward long QT syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "long QT syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "long QT syndrome 1/2, digenic",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "long QT syndrome 1; LQT1",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "ventricular fibrillation with prolonged QT interval",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "long QT syndrome 1, acquired, susceptibility to",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "Ward-Romano syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "LQT1",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "Romano-Ward syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008646",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008646",
            "name": "long QT syndrome 1",
            "description": ""
        },
        {
            "id": "MIM:192500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/192500",
            "name": "Long QT syndrome 1",
            "description": "Long QT syndrome 1"
        }
    ]
}