{
    "disease_id": "DOID:0050967",
    "recommended_name": {
        "id": "DOID:0050967",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050967",
        "name": "spinocerebellar ataxia 17",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by chorea, dementia, dystonia, spasiticity and seizure, has_material_basis_in CAG repeat expansion in the TBP gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia type 17",
            "description": "A rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy."
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "CPD2",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "HDL4",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "Huntington disease-like 4",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "OPCA V",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "OPCA with dementia and extrapyramidal signs",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "SCA 17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "SCA17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "cerebelloparenchymal disorder II",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "olivopontocerebellar atrophy 5",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "olivopontocerebellar atrophy type 5",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia 17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia type 17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia type 17",
            "description": "A rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy."
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "CPD2",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "HDL4",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "Huntington disease-like 4",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "OPCA V",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "OPCA with dementia and extrapyramidal signs",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "SCA 17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "SCA17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "cerebelloparenchymal disorder II",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "olivopontocerebellar atrophy 5",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "olivopontocerebellar atrophy type 5",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia 17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia type 17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia type 17",
            "description": "A rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy."
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "CPD2",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "HDL4",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "Huntington disease-like 4",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "OPCA V",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "OPCA with dementia and extrapyramidal signs",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "SCA 17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "SCA17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "cerebelloparenchymal disorder II",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "olivopontocerebellar atrophy 5",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "olivopontocerebellar atrophy type 5",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia 17",
            "description": ""
        },
        {
            "id": "MONDO:0011781",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011781",
            "name": "spinocerebellar ataxia type 17",
            "description": ""
        },
        {
            "id": "MIM:607136",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607136",
            "name": "Spinocerebellar ataxia 17",
            "description": "Spinocerebellar ataxia 17"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050967"
    ],
    "unlinked_id_list": []
}