Visualize Submit Comment

Metadata
ID	DOID:0050971
Name	spinocerebellar ataxia type 20
Definition	An autosomal dominant cerebellar ataxia that is characterized by cerebellar dysarthria. https://rarediseases.info.nih.gov/diseases/9997/spinocerebellar-ataxia-20
Xrefs	GARD:9997 OMIM:608687
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant cerebellar ataxia