UMLS:C0238111 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0238111 (Lennox-Gastaut syndrome)
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Human Gene/Protein
Chromodomain-helicase-DNA-binding protein 2	15.2
IRF2BPL	13.6
CLCN4	11.7
XLIS	11.6
KPNA7	11.6
ALG13	11.6
LGS	11.4
KCNT2	11.3
CHD2	11.2
STXBP1	11.1
KCNT1	10.9
DNM1	10.9
IQSEC2	10.9
ST3GAL3	10.8
SMEI	10.8
ARFGEF2	10.7
SLACK	10.7
brefeldin A-inhibited	10.6
GABRA1	10.5
GABRB2	10.4

Disease
Lennox-Gastaut syndrome	15.2
epilepsy; symptomatic	15.2
Lennox-Gastaut syndrome	15.1
Nodding spasm	14.2
Atypical absence seizures	14.0
Benign neonatal seizures	13.9
Gurrieri syndrome	13.6
Myoclonic Encephalopathy	13.4
Atypical benign partial epilepsy	13.4
Epilepsy with myoclonic absences	13.4
Benign focal epilepsy of childhood	13.2
Childhood epilepsy with occipital paroxysms	13.2
atonic seizure	13.1
Other epilepsy	12.9
epileptic twilight state	12.7
hypsarhythmia	12.7
Ohtahara syndrome	12.6
Myoclonic astatic epilepsy	12.6
Benign myoclonic epilepsy in infancy	12.4
ABPE	12.2

Enzyme
CYP46A1	7.7
dihydropteridine reductase	7.5
PHT	7.2
GABA transaminase	7.1
CPS	4.9
triphosphatase	4.6
sialyltransferase	4.6
sialyltransferase	4.6
sialyltransferase	4.6
CYP3A4	4.5
tryptophan hydroxylase	4.4
glutamate decarboxylase	4.1
carboxylesterase	3.6
pyruvate dehydrogenase	3.4
pyruvate dehydrogenase	3.4
enolase	3.3
P-glycoprotein	3.1
complex I	3.1
transglutaminase	2.9
glutamine synthetase	2.9