{
    "disease_id": "DOID:0050974",
    "recommended_name": {
        "id": "DOID:0050974",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050974",
        "name": "spinocerebellar ataxia 25",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, has_material_basis_in repeat CAG expansion on chromosome 2p15-p21."
    },
    "synonyms": [
        {
            "id": "MONDO:0012103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012103",
            "name": "spinocerebellar ataxia type 25",
            "description": "Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by cerebellar ataxia and prominent sensory neuropathy."
        },
        {
            "id": "MONDO:0012103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012103",
            "name": "SCA25",
            "description": ""
        },
        {
            "id": "MONDO:0012103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012103",
            "name": "spinocerebellar ataxia 25",
            "description": ""
        },
        {
            "id": "MIM:608703",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608703",
            "name": "Spinocerebellar ataxia 25",
            "description": "Spinocerebellar ataxia 25"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050974"
    ],
    "unlinked_id_list": []
}