OBO ID: DOID:0050959
Term Name: spinocerebellar ataxia type 8 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by slowly progressive dysarthria, bradykinesia, nystagmus and loss of coordination, has_material_basis_in mutation in the ATXN80S gene. https://rarediseases.info.nih.gov/diseases/4956/spinocerebellar-ataxia-8
References:
Ontology: Human Disease   ( DOID:0050959 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 8 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ATXN8 Spinocerebellar ataxia 8
ATXN8OS Spinocerebellar ataxia 8
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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.