{
    "disease_id": "DOID:0111742", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014776", 
            "name": "spinocerebellar ataxia type 42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014776", 
            "name": "spinocerebellar ataxia 42; SCA42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014776", 
            "name": "spinocerebellar ataxia 42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014776", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014776", 
            "name": "SCA42"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111742", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111742", 
            "name": "SCA42"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111742", 
        "description": "An autosomal dominant cerebellar ataxia characterized by gait instability, dysarthria, nystagmus, and saccadic pursuits with variable age of onset and severity and slow progression that has_material_basis_in heterozygous mutation of the CACNA1G gene on chromosome 17q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111742", 
        "name": "cerebellar ataxia type 42"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111742#disease-associations", 
            "id": "0111742", 
            "database": "Alliance of Genome Resources"
        }
    ]
}