{
    "disease_id": "DOID:0050979",
    "recommended_name": {
        "id": "DOID:0050979",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050979",
        "name": "spinocerebellar ataxia type 30",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0013241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013241",
            "name": "spinocerebellar ataxia type 30",
            "description": "Spinocerebellar ataxia type 30 (SCA30) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III; see this term) characterized by a slowly progressive and relatively pure ataxia."
        },
        {
            "id": "MONDO:0013241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013241",
            "name": "spinocerebellar ataxia 30",
            "description": ""
        },
        {
            "id": "MONDO:0013241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013241",
            "name": "spinocerebellar ataxia 30; SCA30",
            "description": ""
        },
        {
            "id": "MONDO:0013241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013241",
            "name": "SCA30",
            "description": ""
        },
        {
            "id": "MONDO:0013241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013241",
            "name": "spinocerebellar ataxia type 30",
            "description": ""
        }
    ]
}