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Metadata
ID	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
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant cerebellar ataxia