Term Name: | spinocerebellar ataxia type 15 |
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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 ) |