Term Name: spinocerebellar ataxia type 23
Synonyms:
Definition: An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene.
Ontology: Human Disease [DOID:0050973]   ( DOID:0050973 )

Relationships
is a type of: autosomal dominant cerebellar ataxia