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DOID DOID:0050973
Name spinocerebellar ataxia type 23
Definition An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene.
https://rarediseases.info.nih.gov/diseases/9950/spinocerebellar-ataxia-23
Xrefs

OMIM:610245

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is_a autosomal dominant cerebellar ataxia

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