{
    "disease_id": "DOID:0110218", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011001", 
            "name": "SCN5A Brugada syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011001", 
            "name": "sudden unexplained nocturnal death syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011001", 
            "name": "Brugada syndrome caused by mutation in SCN5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011001", 
            "name": "Brugada syndrome 1; BRGDA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011001", 
            "name": "right bundle branch block, St segment elevation, and sudden death syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011001", 
            "name": "Brugada syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011001", 
            "name": "BRGDA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011001", 
            "name": "Cardiac conduction defect, nonspecific"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110218", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110218", 
            "name": "BRGDA1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110218", 
        "description": "A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110218", 
        "name": "Brugada syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110218#disease-associations", 
            "id": "0110218", 
            "database": "Alliance of Genome Resources"
        }
    ]
}