OBO ID: DOID:0050985
Term Name: spinocerebellar ataxia type 38 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and nystagmus, presenting in mid-adulthood, and has_material_basis_in mutation to the ELOVL5 gene. https://www.omim.org/entry/615957
References:
Ontology: Human Disease   ( DOID:0050985 )
Relationships
is a type of:
OTHER spinocerebellar ataxia type 38 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ELOVL5 Spinocerebellar ataxia 38 615957
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.