Metadata | |
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ID | 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 |
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