Term Name:	spinocerebellar ataxia type 2
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene.
Ontology:	Human Disease [DOID:0050955]   ( DOID:0050955 )