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Metadata
ID	DOID:0050959
Name	spinocerebellar ataxia type 8
Definition	An autosomal dominant cerebellar ataxia that is characterized by slowly progressive dysarthria, bradykinesia, nystagmus and loss of coordination, has_material_basis_in mutation in the ATXN80S gene. https://rarediseases.info.nih.gov/diseases/4956/spinocerebellar-ataxia-8
Xrefs	OMIM:608768
Parent Relationships	is_a autosomal dominant cerebellar ataxia