{
    "disease_id": "DOID:0050965",
    "recommended_name": {
        "id": "DOID:0050965",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050965",
        "name": "spinocerebellar ataxia type 15",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, nystagmus, dysarthria and dysphagia, has_material_basis_in mutation in the ITPR1 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0050965",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050965",
            "name": "spinocerebellar ataxia type 16",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "spinocerebellar ataxia type 15/16",
            "description": "Spinocerebellar ataxia type 15/16 (SCA15/16) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by cerebellar ataxia, tremor and cognitive impairment."
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "spinocerebellar ataxia 15",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "SCA15/16",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "spinocerebellar ataxia type 15",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "SCA15",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "SCA16 (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "spinocerebellar ataxia 16, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "spinocerebellar ataxia 16",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "spinocerebellar ataxia 15; SCA15",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "spinocerebellar ataxia 16 (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0011694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011694",
            "name": "spinocerebellar ataxia type 15/16",
            "description": ""
        },
        {
            "id": "MIM:606658",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606658",
            "name": "Spinocerebellar ataxia 15",
            "description": "Spinocerebellar ataxia 15"
        }
    ]
}