Search Ontology:
Human Disease

spinocerebellar ataxia type 25

Term ID
DOID:0050974
Synonyms
Definition
An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, has_material_basis_in repeat CAG expansion on chromosome 2p15-p21. https://rarediseases.info.nih.gov/diseases/9996/spinocerebellar-ataxia-25
References
Ontology
Human Disease   ( DOID:0050974 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.