{
    "disease_id": "DOID:0050968", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011397", 
            "name": "autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011397", 
            "name": "autosomal dominant cerebellar ataxia, deafness, and narcolepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011397", 
            "name": "cerebellar ataxia, deafness, and narcolepsy, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011397", 
            "name": "ADCA-DN syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011397", 
            "name": "ADCADN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011397", 
            "name": "ADCA-DN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011397", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011397", 
            "name": "cerebellar ataxia, deafness, and narcolepsy, autosomal dominant; ADCADN"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050968", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by ataxia, sensorineal deafness, narcolepsy with cataplexy, and dementia, has_material_basis_in mutation in the DNMT1 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050968", 
        "name": "autosomal dominant cerebellar ataxia, deafness and narcolepsy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050968#disease-associations", 
            "id": "0050968", 
            "database": "Alliance of Genome Resources"
        }
    ]
}