Term Name:	spinocerebellar ataxia type 10
Synonyms:
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.
Ontology:	Human Disease [DOID:0050960]   ( DOID:0050960 )