| Term Name: | spinocerebellar ataxia 15 |
|---|---|
| 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. |
| Ontology: | Human Disease [DOID:0050965] ( DOID:0050965 ) |