{
    "disease_id": "DOID:0060694", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011025", 
            "name": "cerebellar ataxia, CAYMAN type; ATCAY"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011025", 
            "name": "ATCAY"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011025", 
            "name": "Cayman cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011025", 
            "name": "Cayman ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011025", 
            "name": "cerebellar ataxia, Cayman type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060694", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060694", 
            "name": "Cayman cerebellar ataxia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060694", 
        "description": "An autosomal recessive cerebellar ataxia characterized by marked autosomal recessive inheritance, psychomotor retardation, cerebellar dysfunction including nystagmus, intention tremor, dysarthria, and wide-based ataxic gait, hypotonia and the absence of retinal abnormalities that has_material_basis_in mutation in the ATCAY gene on chromosome 19p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060694", 
        "name": "Cayman type cerebellar ataxia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060694#disease-associations", 
            "id": "0060694", 
            "database": "Alliance of Genome Resources"
        }
    ]
}