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

OMIM:604432

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is_a autosomal dominant cerebellar ataxia

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