spinocerebellar ataxia type 38

Term ID

DOID:0050985

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. https://www.omim.org/entry/615957

References

• OMIM:615957

Ontology

Human Disease   ( DOID:0050985 )