| Metadata | |
|---|---|
| ID | DOID:0050961 |
| Name | spinocerebellar ataxia type 11 |
| Definition | An autosomal dominant cerebellar ataxia that is characterized by ataxia, nystagmus, pyramidal abnormalities and peripheral neuropathy, has_material_basis_in mutation in the TTBK2 gene. https://rarediseases.info.nih.gov/diseases/10475/spinocerebellar-ataxia-11 |
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