MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Protein S
[NCBI]
Gene
Gene
Link
Information
Gain
01
PROSP
[NCBI]
0.000564273
PROS1
[NCBI]
0.000224899
F5
[NCBI]
4.60557e-05
PROC
[NCBI]
4.57033e-05
F2
[NCBI]
3.15439e-05
C4BPA
[NCBI]
3.12305e-05
TYRO3
[NCBI]
2.98543e-05
TFPI
[NCBI]
1.95307e-05
VWF
[NCBI]
1.74065e-05
C4BPB
[NCBI]
1.47573e-05
EGF
[NCBI]
1.29512e-05
PROCR
[NCBI]
9.78926e-06
MERTK
[NCBI]
8.90715e-06
MTHFR
[NCBI]
8.34733e-06
F10
[NCBI]
7.72763e-06
PLG
[NCBI]
6.31063e-06
C4B
[NCBI]
4.57999e-06
F8
[NCBI]
4.49371e-06
SHBG
[NCBI]
3.8839e-06
GGCX
[NCBI]
3.13455e-06
OSM
[NCBI]
2.97844e-06
SERPINC1
[NCBI]
2.61596e-06
VKORC1
[NCBI]
2.16974e-06
SP1
[NCBI]
1.97999e-06
PF4
[NCBI]
1.79195e-06
SERPINE1
[NCBI]
1.70103e-06
F8A1
[NCBI]
1.69451e-06
LRG1
[NCBI]
1.55111e-06
CALU
[NCBI]
1.51354e-06
CST3
[NCBI]
1.47311e-06
PROZ
[NCBI]
1.47298e-06
GAS6
[NCBI]
1.4249e-06
HABP2
[NCBI]
1.40668e-06
GLRX
[NCBI]
1.25113e-06
MSR1
[NCBI]
1.2232e-06
F11
[NCBI]
1.2232e-06
CPB2
[NCBI]
1.20887e-06
THBD
[NCBI]
1.15365e-06
FOXA1
[NCBI]
1.1514e-06
F9
[NCBI]
1.08255e-06
MAN1C1
[NCBI]
1.08255e-06
A2M
[NCBI]
1.07911e-06
F2R
[NCBI]
1.0774e-06
FOXA2
[NCBI]
1.05935e-06
TFPI2
[NCBI]
1.02799e-06
PIGA
[NCBI]
1.01831e-06
ITGAM
[NCBI]
9.987e-07
F3
[NCBI]
9.79279e-07
MGP
[NCBI]
9.18004e-07
CREB1
[NCBI]
8.93288e-07
EPO
[NCBI]
8.8241e-07
SP3
[NCBI]
8.62356e-07
DAG1
[NCBI]
8.50659e-07
ESR2
[NCBI]
8.27429e-07
MPL
[NCBI]
7.90927e-07
AMBP
[NCBI]
7.83657e-07
CLU
[NCBI]
7.61483e-07
ADAMTS13
[NCBI]
7.31456e-07
TNF
[NCBI]
7.05668e-07
PGR
[NCBI]
6.91205e-07
CTSG
[NCBI]
6.25723e-07
CYP2C9
[NCBI]
5.6874e-07
ESR1
[NCBI]
5.58418e-07
PLAUR
[NCBI]
4.74734e-07
JAK2
[NCBI]
4.73003e-07
LIF
[NCBI]
4.47062e-07
STAT3
[NCBI]
4.02296e-07
VEGFA
[NCBI]
2.98858e-07
PTH
[NCBI]
1.65097e-07
OMIM
OMIM
Link
Information
gain
01
PROS1
[NCBI]
0.00157511
SLE
[NCBI]
0.000551658
protein c deficiency, congenital thrombotic disease due to
[NCBI]
0.000170528
legg-calve-perthes disease
[NCBI]
0.000134642
TFPI
[NCBI]
0.000123636
thrombophilia due to deficiency of activated protein c cofactor
[NCBI]
0.000121158
budd-chiari syndrome
[NCBI]
0.000116579
afibrinogenemia, congenital
[NCBI]
9.98001e-05
vitamin k-dependent clotting factors, combined deficiency of, 1
[NCBI]
9.79079e-05
coumarin resistance
[NCBI]
9.30308e-05
PLG
[NCBI]
5.79677e-05
factor v deficiency
[NCBI]
5.71356e-05
RA
[NCBI]
5.41605e-05
MERTK
[NCBI]
5.40072e-05
GGCX
[NCBI]
5.09292e-05
EGF
[NCBI]
5.06718e-05
antithrombin iii deficiency
[NCBI]
4.997e-05
F3
[NCBI]
4.05842e-05
OSM
[NCBI]
3.2066e-05
PCI
[NCBI]
2.84099e-05
CALU
[NCBI]
2.74448e-05
C4BPB
[NCBI]
2.74448e-05
TYRO3
[NCBI]
2.74448e-05
AXL
[NCBI]
2.65502e-05
GAS6
[NCBI]
2.45217e-05
SHBG
[NCBI]
1.78312e-05
FGG
[NCBI]
1.64443e-05
PF4
[NCBI]
1.36426e-05
HNF1A
[NCBI]
1.22902e-05
VEGF
[NCBI]
9.6587e-06
STAT3
[NCBI]
5.57214e-06
PTH
[NCBI]
2.74079e-06
TNF
[NCBI]
1.49541e-06
EPO
[NCBI]
5.67601e-07
Database Center for Life Science