Term Name:	spinocerebellar ataxia 11
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by ataxia, nystagmus, pyramidal abnormalities and peripheral neuropathy, has_material_basis_in mutation in the TTBK2 gene.
Ontology:	Human Disease [DOID:0050961]   ( DOID:0050961 )