{
    "disease_id": "DOID:0080063", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013645", 
            "name": "autosomal recessive syndromic cerebellar ataxia caused by mutation in SYT14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013645", 
            "name": "spinocerebellar ataxia, autosomal recessive 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013645", 
            "name": "SCAR11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013645", 
            "name": "autosomal recessive cerebellar ataxia-psychomotor retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013645", 
            "name": "spinocerebellar ataxia, autosomal recessive 11; SCAR11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013645", 
            "name": "spinocerebellar ataxia, autosomal recessive type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013645", 
            "name": "SYT14 autosomal recessive syndromic cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013645", 
            "name": "autosomal recessive spinocerebellar ataxia type 11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080063", 
        "description": "An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the SYT14 gene on chromosome 1q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080063", 
        "name": "autosomal recessive spinocerebellar ataxia 11"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080063#disease-associations", 
            "id": "0080063", 
            "database": "Alliance of Genome Resources"
        }
    ]
}