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01 Epilepsies, Partial [NCBI]


Gene


Gene Link Information
Gain
01
PPR [NCBI] 0.000598853
FPEVF [NCBI] 0.000352784
EPPS [NCBI] 0.000352784
BFIC [NCBI] 0.000198462
GTS [NCBI] 0.000112745
SCN1A [NCBI] 7.51685e-05
LGI1 [NCBI] 5.41042e-05
PRL [NCBI] 2.59985e-05
SCN2A [NCBI] 2.1122e-05
TRH [NCBI] 1.41493e-05
CACNA1A [NCBI] 1.28702e-05
LDB2 [NCBI] 1.25175e-05
CYP2C19 [NCBI] 1.23438e-05
PCDH19 [NCBI] 1.17381e-05
TRDN [NCBI] 1.14507e-05
GABRD [NCBI] 1.12046e-05
CYP3A4 [NCBI] 1.10002e-05
ADAM22 [NCBI] 1.07985e-05
GRIA2 [NCBI] 1.06266e-05
GRIA3 [NCBI] 1.04704e-05
ICAM5 [NCBI] 1.01952e-05
CNTNAP2 [NCBI] 9.85081e-06
SHBG [NCBI] 9.68909e-06
ALX4 [NCBI] 9.56424e-06
CACNA2D1 [NCBI] 9.56424e-06
DLG4 [NCBI] 9.31883e-06
MAP1B [NCBI] 9.17282e-06
GRID2 [NCBI] 9.0383e-06
SCN1B [NCBI] 8.91359e-06
GABRA1 [NCBI] 8.68854e-06
GRIN1 [NCBI] 8.63662e-06
MLLT3 [NCBI] 8.4897e-06
KCNA1 [NCBI] 8.31161e-06
CHRNB2 [NCBI] 8.22908e-06
DBI [NCBI] 8.15036e-06
CCNA2 [NCBI] 7.96811e-06
ALDH5A1 [NCBI] 7.83516e-06
CCNB1 [NCBI] 7.80348e-06
EPM2A [NCBI] 7.77238e-06
BDNF [NCBI] 7.53442e-06
KCNQ2 [NCBI] 7.36341e-06
MSN [NCBI] 7.0744e-06
GLI3 [NCBI] 7.05408e-06
CDC2 [NCBI] 7.05408e-06
POLG [NCBI] 6.69174e-06
TPP1 [NCBI] 6.50655e-06
ATXN2 [NCBI] 6.26204e-06
GRM5 [NCBI] 5.56776e-06
CYP2C9 [NCBI] 4.9302e-06
ABCG2 [NCBI] 4.59676e-06
MS [NCBI] 4.56163e-06
MECP2 [NCBI] 4.31227e-06
FMR1 [NCBI] 3.25482e-06




OMIM


OMIM Link Information
gain
01
epilepsy, partial, with variable foci [NCBI] 0.00197839
EIG [NCBI] 0.00150537
PPR [NCBI] 0.00125995
ETL2 [NCBI] 0.00113107
RESDAD [NCBI] 0.000984578
ETL4 [NCBI] 0.000984578
epilepsy, partial, with pericentral spikes [NCBI] 0.000984578
polymicrogyria, unilateral [NCBI] 0.000766909
CPD2 [NCBI] 0.000766909
EFMR [NCBI] 0.000592366
convulsions, benign familial infantile, 1 [NCBI] 0.000534964
ECA1 [NCBI] 0.000534964
centralopathic epilepsy [NCBI] 0.000433789
FEB1 [NCBI] 0.000433789
TS [NCBI] 0.000416509
BOE [NCBI] 0.000240764
ADLTE [NCBI] 0.000145404
FSHMD1A [NCBI] 0.000138391
mental retardation syndrome, belgian type [NCBI] 0.000120229
cortical dysplasia-focal epilepsy syndrome [NCBI] 0.000120229
LGI1 [NCBI] 0.000115252
SCN1A [NCBI] 0.000104794
PRL [NCBI] 0.00010165
LKS [NCBI] 9.86321e-05
epilepsy, nocturnal frontal lobe, type 3 [NCBI] 8.92934e-05
JAE [NCBI] 7.6454e-05
myoclonus and ataxia [NCBI] 7.6454e-05
basal ganglia disease, adult-onset [NCBI] 7.6454e-05
hypotension, orthostatic [NCBI] 7.37493e-05
ADAM22 [NCBI] 7.2176e-05
CNTNAP2 [NCBI] 7.2176e-05
FCDT [NCBI] 7.14352e-05
DRPLA [NCBI] 6.91638e-05
encephalopathy, neonatal severe, due to mecp2 mutations [NCBI] 6.45378e-05
myoclonic epilepsy, neonatal, with suppression-burst pattern [NCBI] 6.19564e-05
GABRA1 [NCBI] 6.10901e-05
CHRNB2 [NCBI] 5.90902e-05
GEFS+ [NCBI] 5.68953e-05
ABCC1 [NCBI] 5.53451e-05
EBN1 [NCBI] 5.52502e-05
KCNA1 [NCBI] 5.26608e-05
KCNQ2 [NCBI] 4.94573e-05
MAP1B [NCBI] 4.70416e-05
SPG3A [NCBI] 4.48004e-05
SMEI [NCBI] 4.44048e-05
meningioma, familial [NCBI] 4.32753e-05
SHBG [NCBI] 3.93645e-05
DBI [NCBI] 3.85842e-05
SLE [NCBI] 3.80208e-05
CACNA1A [NCBI] 3.75112e-05
ABCG2 [NCBI] 3.05538e-05
SCA1 [NCBI] 3.04036e-05
BDNF [NCBI] 2.81459e-05
FRDA [NCBI] 2.8011e-05
MECP2 [NCBI] 2.79622e-05
GAPDH [NCBI] 1.89748e-05
GNRH1 [NCBI] 1.86663e-05
MJD [NCBI] 1.63596e-05
AS [NCBI] 1.32191e-05
GTS [NCBI] 1.05013e-05
CD [NCBI] 4.99947e-06
CJD [NCBI] 1.15606e-06




Database Center for Life Science