Search Ontology:
Human Disease
spinocerebellar ataxia type 36
- Term ID
- DOID:0050983
- Synonyms
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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
- References
- Ontology
- Human Disease ( DOID:0050983 )
- is a type of
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Genes Involved
Zebrafish Models