{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014156", 
            "name": "atrial fibrillation, familial, 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014156", 
            "name": "atrial fibrillation, familial, type 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014156", 
            "name": "SCN2B familial atrial fibrillation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014156", 
            "name": "ATFB14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014156", 
            "name": "atrial fibrillation, familial, 14; ATFB14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014156", 
            "name": "familial atrial fibrillation caused by mutation in SCN2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050650", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050650", 
            "name": "ATFB"
        }, 
        {
            "url": "https://www.omim.org/entry/615378", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615378", 
            "name": "Atrial fibrillation, familial, 14"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050650", 
        "description": "An atrial fibrillation that has_material_basis_in autosomal dominant inheritance of the familial atrial fibrillation (ATFB) genes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050650", 
        "name": "familial atrial fibrillation"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615378", 
            "id": "615378", 
            "database": "MIM"
        }
    ]
}