Term Name:	spinocerebellar ataxia type 15
Synonyms:	spinocerebellar ataxia type 16
Definition:	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, nystagmus, dysarthria and dysphagia, has_material_basis_in mutation in the ITPR1 gene.
Ontology:	Human Disease [DOID:0050965]   ( DOID:0050965 )