{
    "disease_id": "DOID:0111616",
    "recommended_name": {
        "id": "DOID:0111616",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111616",
        "name": "autosomal recessive spinocerebellar ataxia 27",
        "description": "An autosomal recessive cerebellar ataxia characterized by adult onset of progressive gait difficulties and other cerebellar signs that has_material_basis_in homozygous or compound heterozygous mutation in the GDAP2 gene on chromosome 1p12."
    },
    "synonyms": [
        {
            "id": "DOID:0111616",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111616",
            "name": "SCAR27",
            "description": ""
        },
        {
            "id": "MONDO:0032706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032706",
            "name": "spinocerebellar ataxia, autosomal recessive 27",
            "description": ""
        },
        {
            "id": "MONDO:0032706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032706",
            "name": "SCAR27",
            "description": ""
        },
        {
            "id": "MIM:618369",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618369",
            "name": "Spinocerebellar ataxia, autosomal recessive, 27",
            "description": "Spinocerebellar ataxia, autosomal recessive, 27"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111616"
    ],
    "unlinked_id_list": []
}