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01 Epilepsy, Tonic-Clonic [NCBI]


Gene


Gene Link Information
Gain
01
ECA1 [NCBI] 0.000633507
BAFME2 [NCBI] 0.000373825
PPR [NCBI] 0.000167079
KCNQ2 [NCBI] 1.92014e-05
POLG [NCBI] 1.78439e-05
PCDH19 [NCBI] 1.27529e-05
KCNQ5 [NCBI] 1.24654e-05
L2HGDH [NCBI] 1.20042e-05
TNNI1 [NCBI] 1.20042e-05
MS [NCBI] 1.14177e-05
SCO1 [NCBI] 1.13417e-05
GRID2 [NCBI] 1.00519e-05
TH [NCBI] 9.37665e-06
CHRNA4 [NCBI] 9.28265e-06
ASPA [NCBI] 9.1249e-06
AAAS [NCBI] 9.01545e-06
RAB27A [NCBI] 8.98047e-06
TNNI3 [NCBI] 8.69421e-06
SCN1A [NCBI] 8.25729e-06
ATP1A2 [NCBI] 8.19058e-06
PHOX2B [NCBI] 7.8022e-06
PRL [NCBI] 6.90035e-06
CYP2D6 [NCBI] 6.67576e-06
CACNA1A [NCBI] 6.24392e-06
KCNQ1 [NCBI] 5.92324e-06
PDGFA [NCBI] 5.86143e-06
MECP2 [NCBI] 5.30376e-06
SLC6A4 [NCBI] 4.55983e-06
TRH [NCBI] 3.84324e-06
CAT [NCBI] 3.58017e-06
ACHE [NCBI] 3.47371e-06
MBP [NCBI] 3.10209e-06
GFAP [NCBI] 2.61568e-06
NGF [NCBI] 2.53635e-06
PTH [NCBI] 1.71376e-06




OMIM


OMIM Link Information
gain
01
ECA1 [NCBI] 0.00138221
EIG4 [NCBI] 0.00101415
FEB9 [NCBI] 0.00101415
EIG [NCBI] 0.000939698
CPD2 [NCBI] 0.000796434
epilepsy, myoclonic, benign adult familial, type 2 [NCBI] 0.000796434
EFMR [NCBI] 0.000621736
CLN4B [NCBI] 0.000564232
kohlschutter-tonz syndrome [NCBI] 0.000541934
folic acid, transport defect involving [NCBI] 0.00052247
ETL2 [NCBI] 0.000475624
epilepsy, myoclonic, benign adult familial, type 1 [NCBI] 0.000462747
AOS [NCBI] 0.000284621
PPR [NCBI] 0.000270777
EKD1 [NCBI] 0.00021507
epilepsy, benign neonatal, autosomal recessive [NCBI] 0.000125147
mental retardation syndrome, belgian type [NCBI] 0.000125147
SMEI [NCBI] 0.000121437
split-foot deformity with mandibulofacial dysostosis [NCBI] 9.42065e-05
schizencephaly [NCBI] 9.42065e-05
epilepsy, reading [NCBI] 8.87053e-05
JRKL [NCBI] 8.86222e-05
CVG/MR [NCBI] 8.46164e-05
ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant [NCBI] 8.13594e-05
basal ganglia disease, adult-onset [NCBI] 8.13594e-05
hypotension, orthostatic [NCBI] 7.86521e-05
valproate embryopathy, susceptibility to [NCBI] 7.86521e-05
breath-holding spells [NCBI] 7.86521e-05
radioulnar synostosis [NCBI] 7.63355e-05
porencephaly, familial [NCBI] 7.4311e-05
corpus callosum, agenesis of [NCBI] 7.4311e-05
encephalopathy, neonatal severe, due to mecp2 mutations [NCBI] 6.94279e-05
ACCPN [NCBI] 6.80825e-05
JRK [NCBI] 6.6266e-05
ADLTE [NCBI] 6.56897e-05
COL4A1 [NCBI] 5.74238e-05
lipoid proteinosis of urbach and wiethe [NCBI] 5.72558e-05
myoclonic epilepsy of lafora [NCBI] 5.27316e-05
PKS [NCBI] 5.27316e-05
CADASIL [NCBI] 5.04472e-05
SPG3A [NCBI] 4.96191e-05
SCN1A [NCBI] 4.77604e-05
SLC18A2 [NCBI] 4.65199e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 4.48004e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 4.31199e-05
ASPA [NCBI] 4.29688e-05
CACNA1A [NCBI] 4.01586e-05
NPC1 [NCBI] 3.9582e-05
SCA1 [NCBI] 3.50691e-05
SLC6A4 [NCBI] 3.44565e-05
HPRT1 [NCBI] 3.2695e-05
FRDA [NCBI] 3.2633e-05
TH [NCBI] 3.10072e-05
MECP2 [NCBI] 3.05768e-05
DRPLA [NCBI] 2.84253e-05
INS [NCBI] 2.59161e-05
MJD [NCBI] 2.06135e-05
PRL [NCBI] 1.79004e-05
CAT [NCBI] 1.01372e-05
ACHE [NCBI] 9.19037e-06
CRH [NCBI] 8.24088e-06
MBP [NCBI] 7.53087e-06
AVP [NCBI] 6.74788e-06
GFAP [NCBI] 5.1522e-06
NGFB [NCBI] 4.75806e-06
PTH [NCBI] 1.68736e-06
SLE [NCBI] 1.32416e-06




Database Center for Life Science