Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Clonazepam	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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