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Lennox-Gastaut syndrome

Disease Summary
Associated Targets (37)
Tclin

29

Tbio

6

Tchem

2


Explore Associated Targets
Mondo Description Lennox-Gastaut syndrome (LGS) belongs to the group of severe childhood epileptic encephalopathies.
Disease Ontology Description A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood.
Mondo Term and Equivalent IDs
MONDO:0016532:  Lennox-Gastaut syndrome
GARD:0009912: 
MESH:D065768: 
NCIT:C84816: 
Orphanet:2382: 
SCTID:230418006: 
UMLS:C0238111: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)