{
    "disease_id": "DOID:0050964",
    "recommended_name": {
        "id": "DOID:0050964",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050964",
        "name": "spinocerebellar ataxia type 14",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the PRKCG gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0011540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011540",
            "name": "spinocerebellar ataxia type 14",
            "description": "Spinocerebellar ataxia type 14 (SCA14) is a rare mild subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive ataxia, dysarthria and nystagmus."
        },
        {
            "id": "MONDO:0011540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011540",
            "name": "SCA14",
            "description": ""
        },
        {
            "id": "MONDO:0011540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011540",
            "name": "spinocerebellar ataxia type 14",
            "description": ""
        },
        {
            "id": "MONDO:0011540",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011540",
            "name": "spinocerebellar ataxia 14",
            "description": ""
        },
        {
            "id": "MIM:605361",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605361",
            "name": "Spinocerebellar ataxia 14",
            "description": "Spinocerebellar ataxia 14"
        }
    ]
}