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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,

Xenbase Genes : slc2a1, gabrb3, cacna1h

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


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

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