OBO ID: DOID:0111312
Term Name: idiopathic generalized epilepsy 11 Search Ontology:
Synonyms:
  • EIG11
Definition: An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CLCN2 on chromosome 3q27.1. https://www.ncbi.nlm.nih.gov/pubmed/19710712
References:
Ontology: Human Disease   ( DOID:0111312 )
Relationships
is a type of:
OTHER idiopathic generalized epilepsy 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CLCN2 {Epilepsy, juvenile absence, susceptibility to, 2} 607628
{Epilepsy, juvenile myoclonic, susceptibility to, 8} 607628
{Epilepsy, idiopathic generalized, susceptibility to, 11} 607628
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.