{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013062", 
            "name": "SNTA1 long QT syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013062", 
            "name": "long QT syndrome caused by mutation in SNTA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013062", 
            "name": "long QT syndrome type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013062", 
            "name": "long QT syndrome 12; LQT12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013062", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013062", 
            "name": "LQT12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110653", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110653", 
            "name": "LQT12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110653", 
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110653", 
        "name": "long QT syndrome 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612955", 
            "id": "612955", 
            "database": "MIM"
        }
    ]
}