{
    "disease_id": "DOID:0110226", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014621", 
            "name": "Brugada syndrome 9; BRGDA9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014621", 
            "name": "Brugada syndrome caused by mutation in KCND3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014621", 
            "name": "Brugada syndrome type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014621", 
            "name": "KCND3 Brugada syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014621", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014621", 
            "name": "BRGDA9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110226", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110226", 
            "name": "BRGDA9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110226", 
        "description": "A Brugada syndrome that has_material_basis_in heterozygous mutation in the KCND3 gene on chromosome 1p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110226", 
        "name": "Brugada syndrome 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616399", 
            "id": "616399", 
            "database": "MIM"
        }
    ]
}