{
    "disease_id": "DOID:0111829", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010547", 
            "name": "X-linked progressive cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010547", 
            "name": "spinocerebellar ataxia, X-linked type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010547", 
            "name": "spinocerebellar ataxia, X-linked 1; SCAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010547", 
            "name": "SCAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010547", 
            "name": "OPCA, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010547", 
            "name": "olivopontocerebellar atrophy, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010547", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010547", 
            "name": "spinocerebellar ataxia, X-linked 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111829", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111829", 
            "name": "X-linked progressive cerebellar ataxia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111829", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111829", 
            "name": "SCAX1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111829", 
        "description": "An X-linked cerebellar ataxia characterized by hypotonia at birth, delayed motor development, gait ataxia, difficulty standing, dysarthria, and slow eye movements that has_material_basis_in hemizygous mutation in ATP2B3 on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111829", 
        "name": "X-linked spinocerebellar ataxia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111829#disease-associations", 
            "id": "0111829", 
            "database": "Alliance of Genome Resources"
        }
    ]
}