Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Prothrombin Time [NCBI]


Gene


Gene Link Information
Gain
01
TFPI [NCBI] 4.32611e-05
CYP2C9 [NCBI] 2.73624e-05
VWF [NCBI] 2.19205e-05
F7 [NCBI] 1.27712e-05
F10 [NCBI] 1.07077e-05
F2 [NCBI] 1.01729e-05
VKORC1 [NCBI] 9.44783e-06
F5 [NCBI] 7.67282e-06
F3 [NCBI] 7.03949e-06
PF4 [NCBI] 5.8594e-06
HGF [NCBI] 5.57778e-06
F9 [NCBI] 4.62602e-06
ALB [NCBI] 3.43079e-06
CTGF [NCBI] 3.11862e-06
TPSB2 [NCBI] 3.03034e-06
CYP2C19 [NCBI] 2.96598e-06
TPSAB1 [NCBI] 2.59358e-06
HABP2 [NCBI] 2.5825e-06
CPB2 [NCBI] 2.20877e-06
HPSE [NCBI] 2.15454e-06
A2M [NCBI] 2.03217e-06
CD163 [NCBI] 1.99479e-06
F13A1 [NCBI] 1.97433e-06
PROC [NCBI] 1.90069e-06
CD40LG [NCBI] 1.87937e-06
LCAT [NCBI] 1.87706e-06
RETN [NCBI] 1.73099e-06
PLG [NCBI] 1.60071e-06
F8 [NCBI] 1.54369e-06
LEP [NCBI] 1.42472e-06
CALCA [NCBI] 1.37135e-06
SERPINE1 [NCBI] 1.30497e-06
CD68 [NCBI] 1.21369e-06
CETP [NCBI] 1.14975e-06
IL6 [NCBI] 9.52441e-07
JAK2 [NCBI] 9.49952e-07
TLR4 [NCBI] 8.99659e-07
NOS2 [NCBI] 8.75968e-07
MPO [NCBI] 7.76959e-07
EPO [NCBI] 6.75228e-07
ACHE [NCBI] 6.45566e-07
PTGS2 [NCBI] 5.61386e-07
PTH [NCBI] 5.12896e-07
TNF [NCBI] 2.01054e-07




OMIM


OMIM Link Information
gain
01
scott syndrome [NCBI] 0.0012249
F3 [NCBI] 0.000658838
coumarin resistance [NCBI] 0.000558418
TFPI [NCBI] 0.000375705
afibrinogenemia, congenital [NCBI] 0.000330519
F2 [NCBI] 0.000262185
FGA [NCBI] 0.000246924
factor x deficiency [NCBI] 0.000165895
cyanosis and hepatic disease [NCBI] 0.000150426
factors viii, ix and xi, combined deficiency of [NCBI] 0.000150426
HEMB [NCBI] 0.000143073
SLE [NCBI] 0.000122256
thrombocytosis, benign familial microcytic [NCBI] 0.000105394
halothane hepatitis [NCBI] 9.29751e-05
F5F8D [NCBI] 9.29751e-05
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 8.7614e-05
factor xii deficiency [NCBI] 7.32352e-05
PPH1 [NCBI] 6.91535e-05
thrombocythemia, essential [NCBI] 6.91535e-05
CHAC [NCBI] 6.91535e-05
factor vii deficiency [NCBI] 6.87386e-05
MHA [NCBI] 6.65687e-05
hepatocellular carcinoma [NCBI] 6.5778e-05
NPC1 [NCBI] 5.08751e-05
thrombasthenia of glanzmann and naegeli [NCBI] 4.40711e-05
factor v deficiency [NCBI] 3.51727e-05
PAPSS2 [NCBI] 2.46207e-05
prekallikrein deficiency [NCBI] 2.41654e-05
RA [NCBI] 1.94947e-05
NPC1 [NCBI] 1.91737e-05
F13A1 [NCBI] 1.60837e-05
A2M [NCBI] 1.56659e-05
PF4 [NCBI] 1.56381e-05
CTGF [NCBI] 1.47754e-05
ALB [NCBI] 1.40814e-05
antithrombin iii deficiency [NCBI] 1.27538e-05
FMF [NCBI] 1.25411e-05
CPB2 [NCBI] 1.20309e-05
von willebrand disease [NCBI] 1.10371e-05
IL6 [NCBI] 9.88141e-06
hemophilia a [NCBI] 9.42005e-06
RP [NCBI] 8.27363e-06
PLG [NCBI] 7.82105e-06
HGF [NCBI] 6.74479e-06
CF [NCBI] 5.02645e-06
XDH [NCBI] 2.52655e-06
PTH [NCBI] 2.44492e-06
ACHE [NCBI] 9.68668e-07
EPO [NCBI] 4.91341e-07
CEACAM5 [NCBI] 3.15389e-07
MPO [NCBI] 4.14139e-08




Database Center for Life Science