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Metadata
ID	DOID:0050970
Name	spinocerebellar ataxia type 19/22
Definition	An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor. https://rarediseases.info.nih.gov/diseases/12365/spinocerebellar-ataxia-19-and-22
Xrefs	GARD:12365 OMIM:607346
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant cerebellar ataxia