Term Name:	spinocerebellar ataxia type 35
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by a slowly progressive ataxia, tremor, dysarthria and hyperreflexia, has_material_basis_in mutation in the TGM6 gene.
Ontology:	Human Disease [DOID:0050982]   ( DOID:0050982 )