OBO ID: DOID:0050994
Term Name: episodic ataxia type 6 Search Ontology:
Synonyms:
Definition: An episodic ataxia that is characterized by nystagmus and dysarthria, and has_material_basis_in autosomal dominant inheritance of mutation in the SLC1A3 gene. https://www.omim.org/entry/612656
References:
Ontology: Human Disease   ( DOID:0050994 )
Relationships
is a type of:
OTHER episodic ataxia type 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC1A3 Episodic ataxia, type 6 612656
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.