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MeSH keywords -> Related genes, diseases (OMIM)


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01 Disseminated Intravascular Coagulation [NCBI]


Gene


Gene Link Information
Gain
01
KTWS [NCBI] 0.000332969
TFPI [NCBI] 0.000250009
TNF [NCBI] 4.52569e-05
PLG [NCBI] 3.85225e-05
PF4 [NCBI] 3.16062e-05
F3 [NCBI] 3.14489e-05
VWF [NCBI] 2.72296e-05
ADAMTS13 [NCBI] 2.14929e-05
SERPINE1 [NCBI] 2.08481e-05
ELA2 [NCBI] 1.56354e-05
PROC [NCBI] 1.36272e-05
F7 [NCBI] 1.2792e-05
SERPIND1 [NCBI] 1.07198e-05
HPN [NCBI] 9.60882e-06
PIH [NCBI] 9.09606e-06
F13B [NCBI] 8.9408e-06
TSPAN8 [NCBI] 8.83363e-06
F2 [NCBI] 8.28862e-06
GPX3 [NCBI] 7.67296e-06
CPB2 [NCBI] 6.69877e-06
F2RL3 [NCBI] 6.66938e-06
SERPINC1 [NCBI] 6.42565e-06
PROCR [NCBI] 6.14734e-06
HMGB1 [NCBI] 6.00399e-06
PLAT [NCBI] 5.76646e-06
SERPING1 [NCBI] 5.65127e-06
CD163 [NCBI] 5.55849e-06
F13A1 [NCBI] 5.54352e-06
EVI1 [NCBI] 5.24419e-06
MIF [NCBI] 5.06724e-06
HGF [NCBI] 4.60079e-06
PAX3 [NCBI] 4.32441e-06
FOXO1 [NCBI] 4.26859e-06
MPL [NCBI] 4.22128e-06
ETV6 [NCBI] 3.94657e-06
CTSG [NCBI] 3.92429e-06
CRP [NCBI] 3.57814e-06
F8 [NCBI] 3.3592e-06
SLC2A1 [NCBI] 3.27309e-06
MUC1 [NCBI] 3.019e-06
CD38 [NCBI] 2.80457e-06
F5 [NCBI] 2.66998e-06
MLL [NCBI] 2.66031e-06
CXCL12 [NCBI] 2.30998e-06
HFE [NCBI] 1.65843e-06
IL6 [NCBI] 1.62273e-06
AVP [NCBI] 1.60852e-06
IL1RN [NCBI] 1.36208e-06
NOS2 [NCBI] 1.34044e-06
FASLG [NCBI] 8.86088e-07




OMIM


OMIM Link Information
gain
01
F3 [NCBI] 0.0023711
TFPI [NCBI] 0.00121111
myeloproliferative syndrome, transient [NCBI] 0.000892148
hemangioma-thrombocytopenia syndrome [NCBI] 0.000342594
SLE [NCBI] 0.000200327
PCI [NCBI] 0.000142572
PLG [NCBI] 0.000134022
thrombocytopenic purpura, autoimmune [NCBI] 0.000131947
PF4 [NCBI] 9.1232e-05
respiratory distress syndrome in premature infants [NCBI] 8.88018e-05
CPB2 [NCBI] 8.79648e-05
ALMS [NCBI] 6.0147e-05
VTN [NCBI] 5.58766e-05
CORT [NCBI] 5.06841e-05
sickle cell anemia [NCBI] 4.80374e-05
TNF [NCBI] 4.71677e-05
IFNA2 [NCBI] 4.28199e-05
PAI1 [NCBI] 2.70052e-05
VEGF [NCBI] 2.56362e-05
fructose intolerance, hereditary [NCBI] 2.40116e-05
GIST [NCBI] 2.15747e-05
RA [NCBI] 2.03048e-05
protein c deficiency, congenital thrombotic disease due to [NCBI] 1.88628e-05
FGA [NCBI] 1.84378e-05
factor v deficiency [NCBI] 1.72744e-05
antithrombin iii deficiency [NCBI] 1.50518e-05
SPINK1 [NCBI] 1.09326e-05
lymphoma, non-hodgkin, familial [NCBI] 9.31249e-06
KLK3 [NCBI] 4.89501e-06
GNRH1 [NCBI] 4.82519e-06
AVP [NCBI] 1.27229e-06
HGF [NCBI] 1.19037e-06




Database Center for Life Science