| Metadata | |
|---|---|
| ID | DOID:0050964 |
| Name | spinocerebellar ataxia type 14 |
| Definition | An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the PRKCG gene. https://rarediseases.info.nih.gov/diseases/9867/spinocerebellar-ataxia-14 |
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