OBO ID: DOID:0050983 |
Term Name: | spinocerebellar ataxia type 36 | Search Ontology: | |
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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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Ontology: | Human Disease ( DOID:0050983 ) |
OTHER spinocerebellar ataxia type 36 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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