Search Ontology:
Human Disease

spinocerebellar ataxia type 23

Term ID
DOID:0050973
Synonyms
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. https://rarediseases.info.nih.gov/diseases/9950/spinocerebellar-ataxia-23
References
Ontology
Human Disease   ( DOID:0050973 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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