UMLS:C0238111 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Target Concepts:

Query: UMLS:C0238111 (Lennox-Gastaut syndrome)
861 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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Concepts found in the documents ranked by [ Frequency | Pointwise Mutual Information | Symmetric Conditional Probability ] .

Human Gene/Protein
Sep	67
ACTH	21
GABA	18
MRI	16
Pol	11
Rett syndrome	10
adrenocorticotropic hormone	9
AED	8
beta-endorphin	7
STXBP1	7
SCN1A	7
LGS	6
CBD	6
cytochrome P450	6
CYP2C19	6
GABRB3	6
REM	5
CHD2	5
She	5
X-linked	5
asymmetrical	5
GABRA1	4
sodium channel	4
CYP3A4	4
KCNT1	4
GABA transaminase	3
GTPase	3
P-glycoprotein	3
NMDA receptor	3
TSC2	3
HLA	3
CLB	3
DNM1	3
thyrotropin-releasing hormone	3
CSF	3
TSC1	3
Thyrotropin-releasing hormone	3
GPR55	3
IgA	2
Mol	2
SCN8A	2
LIS1	2
NHS	2
XLIS	2
parvalbumin	2
GABRG2	2
THC	2
ACS	2
ALG13	2
tyrosine hydroxylase	2
EMX2	2
mTOR	2
GABA(A) receptor	2
CDKL5	2
GABRB2	2
DCX	2
IQSEC2	2
BF2	2
FDG	2
filamin A	2
CYP3A	2
HBA	2
dynamin	2
dynamin 1	2
PHA	2
dihydropteridine reductase	2
por	2
zinc finger protein	1
ROS	1
SMEI	1
CYP2B6	1
MEG	1
glutamate binding	1
KCNQ2	1
IRF2BPL	1
EEF1A2	1
myelo	1
fukutin	1
NR1	1
RNS	1

Disease
Lennox-Gastaut syndrome	861
Lennox-Gastaut syndrome	694
epilepsy	583
West	184
encephalopathy	127
Syndrome	56
status epilepticus	53
mental retardation	41
mental retardation	39
tuberous sclerosis	37
complex partial seizures	33
fits	27
Landau-Kleffner syndrome	26
juvenile myoclonic epilepsy	26
cognitive impairment	20
developmental delay	20
focal epilepsy	19
Ohtahara syndrome	19
Cannabis	17
temporal lobe epilepsy	15
encephalitis	15
rash	13
autism	13
petit mal	13
Rett syndrome	11
dysplasia	11
aplastic anemia	11
confusion	10
Down syndrome	9
Alzheimer's disease	9
multiple sclerosis	9
myoclonus epilepsy	8
cerebral palsy	8
AIC	8
generalized seizure	8
depression	8
atonic seizure	7
intellectual impairment	7
aggression	7
febrile convulsions	7
lissencephaly	7
aphasia	6
LGS	6
severe mental retardation	6
migraine	6
photosensitivity	6
brain atrophy	5
diplopia	5
Angelman syndrome	5
SWS	5
Anterior	5
pachygyria	5
IGE	4
brain dysfunction	4
hemiparesis	4
subacute sclerosing panencephalitis	4
stroke	4
Lennox syndrome	4
hypsarhythmia	4
PME	4
tumor	4
developmental disabilities	4
neuronal ceroid lipofuscinosis	3
dysphagia	3
Intractable epilepsy	3
sleep disorders	3
bipolar disorder	3
sleep disturbances	3
pneumonia	3
Leigh syndrome	3
psychosis	3
blindness	3
apraxia	3
hydrocephalus	3
mutism	3
addiction	3
LBD	3
ketosis	3
nystagmus	3
hamartoma	3

Enzyme
CYP3A4	4
P-glycoprotein	3
GABA transaminase	3
dihydropteridine reductase	2
ACS	2
tyrosine hydroxylase	2
complex I	2
transglutaminase	1
enolase	1
triphosphatase	1
sialyltransferase	1
pyruvate dehydrogenase	1
ATPase	1
aspartate aminotransferase	1
CYP46A1	1
superoxide dismutase	1
pyruvate dehydrogenase	1
xanthine oxidase	1
sialyltransferase	1
sialyltransferase	1
alanine aminotransferase	1
CPS	1
carboxylesterase	1
glutamate decarboxylase	1
PHT	1
catalase	1
tryptophan hydroxylase	1
pyruvate dehydrogenase	1
glutamine synthetase	1