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Metadata
DOID DOID:0050960
Name spinocerebellar ataxia type 10
Definition An autosomal dominant cerebellar ataxia that is characterized by gait ataxia, upper-limb ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the ATXN10 gene.
https://www.ncbi.nlm.nih.gov/books/NBK1175/
Xrefs

GARD:10474

OMIM:603516

Relationships

is_a autosomal dominant cerebellar ataxia

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