Term Name:	spinocerebellar ataxia type 5
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression, and has_material_basis_in mutation in the SPTBN2 gene.
Ontology:	Human Disease [DOID:0050882]   ( DOID:0050882 )