{
    "disease_id": "DOID:0050972",
    "recommended_name": {
        "id": "DOID:0050972",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050972",
        "name": "spinocerebellar ataxia 21",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by progressive cerebellar ataxia, cognitive impairment, tremor, bradykinesia and rigidity."
    },
    "synonyms": [
        {
            "id": "MONDO:0011833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011833",
            "name": "spinocerebellar ataxia type 21",
            "description": "Spinocerebellar ataxia type 21 (SCA21) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive cerebellar ataxia, mild cognitive impairment, postural and/or resting tremor, bradykinesia, and rigidity."
        },
        {
            "id": "MONDO:0011833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011833",
            "name": "SCA21",
            "description": ""
        },
        {
            "id": "MONDO:0011833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011833",
            "name": "spinocerebellar ataxia type 21",
            "description": ""
        },
        {
            "id": "MONDO:0011833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011833",
            "name": "spinocerebellar ataxia 21",
            "description": ""
        },
        {
            "id": "MIM:607454",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607454",
            "name": "Spinocerebellar ataxia 21",
            "description": "Spinocerebellar ataxia 21"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050972"
    ],
    "unlinked_id_list": []
}