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| Term | spinocerebellar ataxia type 23 | ID (Ontology) | DOID:0050973 (Human Disease) |
| 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. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal dominant disease__ cerebellar ataxia___________| autosomal dominant cerebellar ataxia |__spinocerebellar ataxia type 23 |
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| Is a | autosomal dominant cerebellar ataxia | ||
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External Crossreferences & Linkouts
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| MIM:610245 | |||