| Metadata | |
|---|---|
| ID | DOID:0050983 |
| Name | spinocerebellar ataxia 36 |
| Definition | An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, sensiorineural hearing loss and muscle atrophy, has_material_basis_in mutation in the NOP56 gene. https://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-36 |
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