{
    "disease_id": "DOID:0050961",
    "recommended_name": {
        "id": "DOID:0050961",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050961",
        "name": "spinocerebellar ataxia 11",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by ataxia, nystagmus, pyramidal abnormalities and peripheral neuropathy, has_material_basis_in mutation in the TTBK2 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0011464",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011464",
            "name": "spinocerebellar ataxia type 11",
            "description": "Spinocerebellar ataxia type 11 (SCA11) is a subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the early-onset of cerebellar signs, eye movement abnormalities and pyramidal signs."
        },
        {
            "id": "MONDO:0011464",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011464",
            "name": "SCA11",
            "description": ""
        },
        {
            "id": "MONDO:0011464",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011464",
            "name": "spinocerebellar ataxia type 11",
            "description": ""
        },
        {
            "id": "MONDO:0011464",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011464",
            "name": "spinocerebellar ataxia 11",
            "description": ""
        },
        {
            "id": "MIM:604432",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604432",
            "name": "Spinocerebellar ataxia 11",
            "description": "Spinocerebellar ataxia 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050961"
    ],
    "unlinked_id_list": []
}