{
    "disease_id": "DOID:0111746", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111746", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111746", 
            "name": "SCA48"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111746", 
        "description": "An autosomal dominant cerebellar ataxia characterized by mid-adult onset of gait ataxia and/or cognitive-affective symptoms that has_material_basis_in heterozygous mutation in STUB1 on chromosome 16p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111746", 
        "name": "cerebellar ataxia type 48"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111746#disease-associations", 
            "id": "0111746", 
            "database": "Alliance of Genome Resources"
        }
    ]
}