{
    "disease_id": "DOID:0111614",
    "recommended_name": {
        "id": "DOID:0111614",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111614",
        "name": "autosomal recessive spinocerebellar ataxia 22",
        "description": "An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111614",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111614",
            "name": "SCAR22",
            "description": ""
        },
        {
            "id": "MONDO:0014845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014845",
            "name": "spinocerebellar ataxia, autosomal recessive 22",
            "description": "Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the VWA3B gene."
        },
        {
            "id": "MONDO:0014845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014845",
            "name": "SCAR22",
            "description": ""
        },
        {
            "id": "MONDO:0014845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014845",
            "name": "VWA3B autosomal recessive cerebellar ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0014845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014845",
            "name": "autosomal recessive cerebellar ataxia caused by mutation in VWA3B",
            "description": ""
        },
        {
            "id": "MONDO:0014845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014845",
            "name": "spinocerebellar ataxia, autosomal recessive 22",
            "description": ""
        },
        {
            "id": "MONDO:0014845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014845",
            "name": "spinocerebellar ataxia, autosomal recessive 22; SCAR22",
            "description": ""
        },
        {
            "id": "MONDO:0014845",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014845",
            "name": "spinocerebellar ataxia, autosomal recessive type 22",
            "description": ""
        },
        {
            "id": "MIM:616948",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616948",
            "name": "Spinocerebellar ataxia, autosomal recessive, 22",
            "description": "Spinocerebellar ataxia, autosomal recessive, 22"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111614"
    ],
    "unlinked_id_list": []
}