Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (1)
DOID:1825 - childhood absence epilepsy

Disease Ontology Definition:A childhood electroclinical syndrome that is characterized by brief and frequent absence seizures in children with age of onset between four and ten years.

Synonyms: absence seizure, petit mal seizure, pyknolepsy

In Mondo Disease Ontology:
MONDO:0010826 - childhood absence epilepsy

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : slc2a1, gabrb3, cacna1h

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): childhood electroclinical syndrome (is_a)