{
    "disease_id": "DOID:0080287",
    "recommended_name": {
        "id": "DOID:0080287",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080287",
        "name": "spinocerebellar ataxia 45",
        "description": "An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the FAT2 gene on chromosome 5q33."
    },
    "synonyms": [
        {
            "id": "MONDO:0033480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033480",
            "name": "spinocerebellar ataxia 45",
            "description": ""
        },
        {
            "id": "MONDO:0033480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033480",
            "name": "spinocerebellar ataxia 45; SCA45",
            "description": ""
        },
        {
            "id": "MONDO:0033480",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033480",
            "name": "SCA45",
            "description": ""
        },
        {
            "id": "MIM:617769",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617769",
            "name": "Spinocerebellar ataxia 45",
            "description": "Spinocerebellar ataxia 45"
        }
    ]
}