{
    "disease_id": "DOID:0111616", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111616", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111616", 
            "name": "SCAR27"
        }, 
        {
            "url": "https://www.omim.org/entry/618369", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:618369", 
            "name": "Spinocerebellar ataxia, autosomal recessive, 27"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111616", 
        "description": "An autosomal recessive cerebellar ataxia characterized by adult onset of progressive gait difficulties and other cerebellar signs  that has_material_basis_in homozygous or compound heterozygous mutation in GDAP2 on chromosome 1p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111616", 
        "name": "autosomal recessive spinocerebellar ataxia 27"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618369", 
            "id": "618369", 
            "database": "MIM"
        }
    ]
}