Term Name:	spinocerebellar ataxia type 36
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, sensiorineural hearing loss and muscle atrophy, has_material_basis_in mutation in the NOP56 gene.
Ontology:	Human Disease [DOID:0050983]   ( DOID:0050983 )