Lennox-Gastaut syndrome

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Summary

Literature (2)

DOID:0050561 - Lennox-Gastaut syndrome

Disease Ontology Definition:n_a

Synonyms: Lennox syndrome

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0016532 - Lennox-Gastaut syndrome

MONDO:0016532 - Lennox-Gastaut syndrome

OMIM:

OMIM:606369 - MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY

OMIM:606369 - MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY

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)