{
    "disease_id": "DOID:0050960",
    "recommended_name": {
        "id": "DOID:0050960",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050960",
        "name": "spinocerebellar ataxia type 10",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by gait ataxia, upper-limb ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the ATXN10 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0011330",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011330",
            "name": "spinocerebellar ataxia type 10",
            "description": "Spinocerebellar ataxia type 10 (SCA10) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive cerebellar syndrome and epilepsy, sometimes mild pyramidal signs, peripheral neuropathy and neuropsychological disturbances."
        },
        {
            "id": "MONDO:0011330",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011330",
            "name": "SCA10",
            "description": ""
        },
        {
            "id": "MONDO:0011330",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011330",
            "name": "spinocerebellar ataxia type 10",
            "description": ""
        },
        {
            "id": "MONDO:0011330",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011330",
            "name": "spinocerebellar ataxia 10",
            "description": ""
        },
        {
            "id": "MIM:603516",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603516",
            "name": "Spinocerebellar ataxia 10",
            "description": "Spinocerebellar ataxia 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050960"
    ],
    "unlinked_id_list": []
}