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DOID 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

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is_a autosomal dominant cerebellar ataxia

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