spinocerebellar ataxia type 36

Term ID

DOID:0050983

Synonyms

Definition

An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, sensiorineural hearing loss and muscle atrophy, has_material_basis_in mutation in the NOP56 gene. https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-36

References

• OMIM:614153

Ontology

Human Disease   ( DOID:0050983 )