Lennox-gastaut syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
LENNOX-GASTAUT SYNDROME
2382C0238111MONDO:0016532
CHD2 Causal
23708187
Disgenet, GWAS catalog, Orphanet —
DNM1 Causal
25262651 25533962
Disgenet, GWAS catalog, Orphanet
GABRG2 Causal — Disgenet
All12 Causal3 Unknown9
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Dravet syndrome 3 shared genesGABRG2, SCN1A, SCN2A Related via 3 shared genes including GABRG2, SCN1A, SCN2A. Hemiplegic migraine 2 shared genesCACNA1A, SCN1A Related via 2 shared genes including CACNA1A, SCN1A. Generalized epilepsy with febrile seizures plus 3 shared genesGABRG2, SCN1A, SCN2A Related via 3 shared genes including GABRG2, SCN1A, SCN2A. Absence epilepsy 2 shared genesCACNA1A, GABRB3 Related via 2 shared genes including CACNA1A, GABRB3. Epilepsy with myoclonic atonic seizures 2 shared genesCHD2, SCN1A Related via 2 shared genes including CHD2, SCN1A.