{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012737", 
            "name": "long QT syndrome type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012737", 
            "name": "atrial fibrillation, familial, 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012737", 
            "name": "long QT syndrome 10; LQT10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012737", 
            "name": "long QT syndrome caused by mutation in SCN4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012737", 
            "name": "SCN4B long QT syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012737", 
            "name": "LQT10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110651", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110651", 
            "name": "LQT10"
        }, 
        {
            "url": "https://www.omim.org/entry/611819", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:611819", 
            "name": "Atrial fibrillation, familial, 17"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110651", 
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110651", 
        "name": "long QT syndrome 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/611819", 
            "id": "611819", 
            "database": "MIM"
        }
    ]
}