Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Clonazepam [NCBI]


Gene


Gene Link Information
Gain
01
PKC [NCBI] 0.000136119
MS [NCBI] 0.000114209
NDUFS7 [NCBI] 2.2635e-06
CLN8 [NCBI] 2.22696e-06
FIS1 [NCBI] 2.10192e-06
TIMM8A [NCBI] 2.03868e-06
GABRB2 [NCBI] 2.02764e-06
GABRA1 [NCBI] 1.94074e-06
GLRA1 [NCBI] 1.90772e-06
PANK2 [NCBI] 1.7338e-06
CSTB [NCBI] 1.6672e-06
TOR1A [NCBI] 1.63423e-06
GRM5 [NCBI] 1.33218e-06
UMOD [NCBI] 1.31628e-06
CHAT [NCBI] 1.01071e-06
CAT [NCBI] 9.98399e-07
LPL [NCBI] 9.84375e-07
TRH [NCBI] 9.59857e-07
CCK [NCBI] 8.70544e-07
CASP3 [NCBI] 7.63746e-07
NGF [NCBI] 7.33815e-07
PRL [NCBI] 7.26551e-07
TNF [NCBI] 5.48288e-07




OMIM


OMIM Link Information
gain
01
epilepsy, myoclonic, benign adult familial, type 1 [NCBI] 0.00192174
EKD1 [NCBI] 0.000994549
SPS [NCBI] 0.000985761
hyperekplexia, hereditary [NCBI] 0.000707573
LKS [NCBI] 0.000214783
branchial myoclonus with spastic paraparesis and cerebellar ataxia [NCBI] 0.000189486
MTS [NCBI] 0.000111108
infantile spasm syndrome, x-linked [NCBI] 0.000111108
PNKD1 [NCBI] 9.91127e-05
myoclonic dystonia [NCBI] 9.05121e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 8.55445e-05
EIG [NCBI] 6.50141e-05
NDUFS7 [NCBI] 4.34567e-05
GLRA1 [NCBI] 3.48229e-05
PD [NCBI] 2.44882e-05
hla-d histocompatibility type [NCBI] 1.6345e-05
SLE [NCBI] 9.50477e-06
CHAT [NCBI] 9.26328e-06
CAT [NCBI] 9.19141e-06
CCK [NCBI] 6.66626e-06
NGFB [NCBI] 4.29315e-06
PRL [NCBI] 4.18089e-06
TNF [NCBI] 2.06451e-06




Database Center for Life Science