Term Name:	spinocerebellar ataxia type 31
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by late-onset ataxia, dysarthria and horizontal nystagmus, has_material_basis_in repeat expansion mutation in the BEAN1 gene.
Ontology:	Human Disease [DOID:0050980]   ( DOID:0050980 )