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MeSH keywords -> Related genes, diseases (OMIM)


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01 Epilepsy, Generalized [NCBI]


Gene


Gene Link Information
Gain
01
PPR [NCBI] 0.00143998
EIG2 [NCBI] 0.000352784
EGI [NCBI] 0.000292051
EKD2 [NCBI] 0.000292051
SCN1A [NCBI] 0.000230076
SCN1B [NCBI] 0.000178581
CLCN2 [NCBI] 6.17779e-05
GABRR2 [NCBI] 6.01054e-05
CACNA1H [NCBI] 5.50971e-05
GABRG2 [NCBI] 5.35612e-05
KCNQ2 [NCBI] 4.47314e-05
KCNQ3 [NCBI] 3.84525e-05
GABRD [NCBI] 3.63343e-05
CACNA1A [NCBI] 3.38837e-05
SCN2A [NCBI] 3.01333e-05
ME2 [NCBI] 2.69882e-05
ARC [NCBI] 2.30769e-05
KCNJ10 [NCBI] 2.25435e-05
SCN2B [NCBI] 2.16763e-05
GABBR1 [NCBI] 1.84515e-05
MS [NCBI] 1.75004e-05
GABRA1 [NCBI] 1.73191e-05
GABRB3 [NCBI] 1.71113e-05
CHRNA4 [NCBI] 1.647e-05
C4orf31 [NCBI] 1.51266e-05
OPRM1 [NCBI] 1.32563e-05
KCNK16 [NCBI] 1.27464e-05
GLRA3 [NCBI] 1.27464e-05
KCNMB3 [NCBI] 1.27464e-05
EFHC2 [NCBI] 1.12649e-05
HCN1 [NCBI] 1.08313e-05
HCN2 [NCBI] 1.04858e-05
GLRB [NCBI] 1.04858e-05
TRDN [NCBI] 1.01985e-05
KCNJ9 [NCBI] 1.01985e-05
KCNJ3 [NCBI] 1.01985e-05
CACNB4 [NCBI] 9.73764e-06
VCX [NCBI] 9.5467e-06
GRIK2 [NCBI] 9.37495e-06
NEDD4L [NCBI] 9.07588e-06
SLC4A3 [NCBI] 9.07588e-06
ALDH7A1 [NCBI] 8.94391e-06
ADSL [NCBI] 8.94391e-06
SLC12A6 [NCBI] 8.82141e-06
KCNJ6 [NCBI] 8.59996e-06
GABRB2 [NCBI] 8.59996e-06
BRD2 [NCBI] 8.40396e-06
CLN8 [NCBI] 8.31379e-06
EFHC1 [NCBI] 8.22815e-06
UGT2B7 [NCBI] 8.06878e-06
KCNMA1 [NCBI] 7.99436e-06
KCNN3 [NCBI] 7.99436e-06
PNMA2 [NCBI] 7.92304e-06
TRPM6 [NCBI] 7.66434e-06
CDKL5 [NCBI] 7.60538e-06
HLA-F [NCBI] 7.49323e-06
CACNA1F [NCBI] 7.33777e-06
ANKH [NCBI] 7.10663e-06
CHRNB2 [NCBI] 6.98169e-06
DBI [NCBI] 6.90323e-06
CHRNA7 [NCBI] 6.68756e-06
ACP1 [NCBI] 6.62138e-06
ALDH5A1 [NCBI] 6.58923e-06
EPM2A [NCBI] 6.52672e-06
HTR2C [NCBI] 6.43709e-06
ATP1A2 [NCBI] 5.93722e-06
SRF [NCBI] 5.91573e-06
TRH [NCBI] 5.66756e-06
SCN4A [NCBI] 5.62276e-06
PRKCE [NCBI] 5.2261e-06
CRH [NCBI] 4.77236e-06
CASR [NCBI] 4.65853e-06
OPRL1 [NCBI] 4.61903e-06
KCNQ1 [NCBI] 3.71088e-06
PAX6 [NCBI] 3.69436e-06
SLC6A3 [NCBI] 3.66721e-06
HP [NCBI] 3.38264e-06
ABCB1 [NCBI] 2.82019e-06
SHBG [NCBI] 2.50814e-06
SLC6A4 [NCBI] 2.4169e-06
FMR1 [NCBI] 2.10993e-06
TH [NCBI] 1.4823e-06
PRL [NCBI] 5.55146e-07




OMIM


OMIM Link Information
gain
01
EIG [NCBI] 0.0105109
PPR [NCBI] 0.00350083
FEB1 [NCBI] 0.00197492
EIG2 [NCBI] 0.00101415
PPR2 [NCBI] 0.00101415
EIG1 [NCBI] 0.00101415
GEFS+ [NCBI] 0.000943499
SMEI [NCBI] 0.000679065
epilepsy, nocturnal frontal lobe, type 2 [NCBI] 0.000621736
SCN1A [NCBI] 0.000604887
EKD2 [NCBI] 0.000590318
epilepsy, myoclonic, benign adult familial, type 1 [NCBI] 0.000462747
JME [NCBI] 0.000367792
JAE [NCBI] 0.000245703
SLE [NCBI] 0.000234843
EKD1 [NCBI] 0.00021507
CLCN2 [NCBI] 0.0002084
GABRG2 [NCBI] 0.000192802
EBN2 [NCBI] 0.000163689
SCN1B [NCBI] 0.000128237
KCNQ3 [NCBI] 0.000128237
ME2 [NCBI] 0.000128237
IDDM [NCBI] 0.000127389
myoclonic epilepsy, neonatal, with suppression-burst pattern [NCBI] 0.000115818
epilepsy, childhood absence, 3 [NCBI] 0.000104234
epilepsy with grand mal seizures on awakening [NCBI] 0.000104234
SPERM [NCBI] 0.000104234
GEPD [NCBI] 7.33318e-05
FEB8 [NCBI] 7.33318e-05
GABRD [NCBI] 6.39723e-05
KCNMA1 [NCBI] 6.39723e-05
3-@methylcrotonyl-coa carboxylase 2 deficiency [NCBI] 6.37796e-05
EFHC1 [NCBI] 6.05968e-05
segawa syndrome, autosomal recessive [NCBI] 6.05416e-05
GABRA1 [NCBI] 5.80874e-05
CACNB4 [NCBI] 5.80874e-05
epilepsy, nocturnal frontal lobe, type 1 [NCBI] 5.355e-05
CHRNA4 [NCBI] 4.79322e-05
KCNQ2 [NCBI] 4.64608e-05
heterotopia, periventricular, x-linked dominant [NCBI] 4.29993e-05
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to [NCBI] 4.20713e-05
OPRM1 [NCBI] 3.76073e-05
MLC [NCBI] 3.61758e-05
DBI [NCBI] 3.56056e-05
CACNA1A [NCBI] 3.45356e-05
SRF [NCBI] 3.03292e-05
ACADM [NCBI] 2.865e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 2.48931e-05
SHBG [NCBI] 1.05186e-05
panencephalitis, subacute sclerosing [NCBI] 6.17568e-06
TH [NCBI] 4.87779e-06
AS [NCBI] 2.63408e-06
PRL [NCBI] 8.04421e-07




Database Center for Life Science