Term Name: spinocerebellar ataxia type 8
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by slowly progressive dysarthria, bradykinesia, nystagmus and loss of coordination, has_material_basis_in mutation in the ATXN80S gene.
Ontology: Human Disease [DOID:0050959]   ( DOID:0050959 )

Relationships
is a type of: autosomal dominant cerebellar ataxia