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Summary Literature (3)
DOID:0050561 - Lennox-Gastaut syndrome

Disease Ontology Definition:A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood.

Synonyms: Lennox syndrome

Xenbase Genes : cux2, chd2, scn1a, dnm1, mapk10, gabrb3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016532 - Lennox-Gastaut syndrome

MIM:
MIM:606369 - MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY

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

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