{
    "disease_id": "DOID:0050968",
    "recommended_name": {
        "id": "DOID:0050968",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050968",
        "name": "autosomal dominant cerebellar ataxia, deafness and narcolepsy",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0011397",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011397",
            "name": "autosomal dominant cerebellar ataxia, deafness and narcolepsy",
            "description": "Autosomal dominant cerebellar ataxia, deafness and narcolepsy (ADCA-DN) is a polymorphic disorder and a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by ataxia, sensorineural deafness and narcolepsy with cataplexy and dementia."
        },
        {
            "id": "MONDO:0011397",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011397",
            "name": "ADCA-DN syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011397",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011397",
            "name": "autosomal dominant cerebellar ataxia, deafness and narcolepsy",
            "description": ""
        },
        {
            "id": "MONDO:0011397",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011397",
            "name": "ADCA-DN",
            "description": ""
        },
        {
            "id": "MONDO:0011397",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011397",
            "name": "ADCADN",
            "description": ""
        },
        {
            "id": "MONDO:0011397",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011397",
            "name": "autosomal dominant cerebellar ataxia, deafness, and narcolepsy",
            "description": ""
        },
        {
            "id": "MONDO:0011397",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011397",
            "name": "autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011397",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011397",
            "name": "cerebellar ataxia, deafness, and narcolepsy, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:604121",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604121",
            "name": "Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant",
            "description": "Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050968"
    ],
    "unlinked_id_list": []
}