{
    "disease_id": "DOID:0080029",
    "recommended_name": {
        "id": "DOID:0080029",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080029",
        "name": "autosomal recessive spinocerebellar ataxia 16",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "autosomal recessive spinocerebellar ataxia 16",
            "description": "Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the STUB1 gene."
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "spinocerebellar ataxia, autosomal recessive type 16",
            "description": ""
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "spinocerebellar ataxia autosomal recessive type 16",
            "description": ""
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "STUB1 autosomal recessive cerebellar ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "spinocerebellar ataxia, autosomal recessive 16; SCAR16",
            "description": ""
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "spinocerebellar ataxia, autosomal recessive 16",
            "description": ""
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "autosomal recessive cerebellar ataxia due to STUB1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "SCAR16",
            "description": ""
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "autosomal recessive cerebellar ataxia caused by mutation in STUB1",
            "description": ""
        },
        {
            "id": "MONDO:0014339",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014339",
            "name": "autosomal recessive spinocerebellar ataxia type 16",
            "description": ""
        },
        {
            "id": "MIM:615768",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615768",
            "name": "Spinocerebellar ataxia, autosomal recessive, 16",
            "description": "Spinocerebellar ataxia, autosomal recessive, 16"
        }
    ]
}