spinocerebellar ataxia type 8

Term ID

DOID:0050959

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. https://rarediseases.info.nih.gov/diseases/4956/spinocerebellar-ataxia-8

References

• OMIM:608768

Ontology

Human Disease   ( DOID:0050959 )