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DOID:0070309 - absence epilepsy
Disease Ontology Definition:An electroclinical syndrome characterized by the occurrence of generalized onset seizures that cause lapses in awareness, begin and end abruptly, typically last only a few seconds and are associated with abnormal spike-wave discharges as seen by electroencephalogram.
Synonyms:
Xenbase Genes
:
cux2,
clcn2,
chd2,
scn1a,
tnrc6a,
cilk1,
dnm1,
grin2a,
adra2b,
mapk10,
efhc1,
cacnb4,
slc2a1,
rapgef2,
gabrg2,
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
electroclinical syndrome (is_a)