{
    "disease_id": "DOID:0080029", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "spinocerebellar ataxia, autosomal recessive type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "spinocerebellar ataxia autosomal recessive type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "STUB1 autosomal recessive cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "spinocerebellar ataxia, autosomal recessive 16; SCAR16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "spinocerebellar ataxia, autosomal recessive 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "autosomal recessive cerebellar ataxia due to STUB1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "SCAR16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "autosomal recessive cerebellar ataxia caused by mutation in STUB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014339", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014339", 
            "name": "autosomal recessive spinocerebellar ataxia type 16"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080029", 
        "description": "An autosomal recessive cerebellar ataxia that is characterized by truncal and limb ataxia resulting in gait instability and that has_material_basis_in homozygous or compound heterozygous mutation in the STUB1 gene on chromosome 16p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080029", 
        "name": "autosomal recessive spinocerebellar ataxia 16"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080029#disease-associations", 
            "id": "0080029", 
            "database": "Alliance of Genome Resources"
        }
    ]
}