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Metadata
ID	DOID:0050972
Name	spinocerebellar ataxia type 21
Definition	An autosomal dominant cerebellar ataxia that is characterized by progressive cerebellar ataxia, cognitive impairment, tremor, bradykinesia and rigidity. https://rarediseases.info.nih.gov/diseases/9999/spinocerebellar-ataxia-21
Xrefs	GARD:9999 OMIM:607454
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant cerebellar ataxia