Search Ontology:
Human Disease

spinocerebellar ataxia 10

Term ID
DOID:0050960
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by gait ataxia, upper-limb ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the ATXN10 gene. https://www.ncbi.nlm.nih.gov/books/NBK1175/
References
Ontology
Human Disease   ( DOID:0050960 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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