{
    "disease_id": "DOID:0070413",
    "recommended_name": {
        "id": "DOID:0070413",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070413",
        "name": "autosomal recessive spinocerebellar ataxia 32",
        "description": "An autosomal recessive cerebellar ataxia characterized by onset of gait ataxia in the second or third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the PRDX3 gene on chromosome 10q26."
    },
    "synonyms": [
        {
            "id": "DOID:0070413",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070413",
            "name": "SCAR32",
            "description": ""
        },
        {
            "id": "MONDO:0859245",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859245",
            "name": "spinocerebellar ataxia, autosomal recessive 32",
            "description": ""
        },
        {
            "id": "MIM:619862",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619862",
            "name": "Spinocerebellar ataxia, autosomal recessive, 32",
            "description": "Spinocerebellar ataxia, autosomal recessive, 32"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070413"
    ],
    "unlinked_id_list": []
}