spinocerebellar ataxia type 15

Term ID

DOID:0050965

Synonyms

• spinocerebellar ataxia type 16

Definition

An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, nystagmus, dysarthria and dysphagia, has_material_basis_in mutation in the ITPR1 gene. https://rarediseases.info.nih.gov/diseases/10477/spinocerebellar-ataxia-15

References

• OMIM:606658

Ontology

Human Disease   ( DOID:0050965 )