Term Name:	spinocerebellar ataxia type 38
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and nystagmus, presenting in mid-adulthood, and has_material_basis_in mutation to the ELOVL5 gene.
Ontology:	Human Disease [DOID:0050985]   ( DOID:0050985 )