{
    "disease_id": "DOID:0110646", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011377", 
            "name": "long QT syndrome 3; LQT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011377", 
            "name": "long QT syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011377", 
            "name": "SCN5A long QT syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011377", 
            "name": "long QT syndrome caused by mutation in SCN5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011377", 
            "name": "long QT syndrome 2/3, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011377", 
            "name": "long QT syndrome 3, acquired, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011377", 
            "name": "long QT syndrome 3/6, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011377", 
            "name": "LQT3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110646", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110646", 
            "name": "LQT3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110646", 
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110646", 
        "name": "long QT syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110646#disease-associations", 
            "id": "0110646", 
            "database": "Alliance of Genome Resources"
        }
    ]
}