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 (0)
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

Xenbase Genes : slc2a1, gabrb3, cacna1h

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010826 - childhood absence epilepsy


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): childhood electroclinical syndrome (is_a)