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Lennox-Gastaut syndrome

MONDO:0016532

Also known as: LGS, encephalopathy of childhood, epileptic encephalopathy Lennox-Gastaut type

MONDO:
MONDO:0016532
Orphanet:
2382
Rare disease34 associated genes

Description

Lennox-Gastaut syndrome (LGS) belongs to the group of severe childhood epileptic encephalopathies.

Associated genes

+24 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.