{
    "disease_id": "DOID:0080259",
    "recommended_name": {
        "id": "DOID:0080259",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080259",
        "name": "autosomal recessive spinocerebellar ataxia 25",
        "description": "An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the ATG5 gene on chromosome 6q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0033115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033115",
            "name": "spinocerebellar ataxia, autosomal recessive 25",
            "description": ""
        },
        {
            "id": "MONDO:0033115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033115",
            "name": "autosomal recessive spinocerebellar ataxia 25",
            "description": ""
        },
        {
            "id": "MONDO:0033115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033115",
            "name": "spinocerebellar ataxia, autosomal recessive 25",
            "description": ""
        },
        {
            "id": "MONDO:0033115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033115",
            "name": "SCAR25",
            "description": ""
        },
        {
            "id": "MIM:617584",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617584",
            "name": "Spinocerebellar ataxia, autosomal recessive, 25",
            "description": "Spinocerebellar ataxia, autosomal recessive, 25"
        }
    ]
}