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01 Blood Coagulation Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
IGAN [NCBI] 0.000171286
VWF [NCBI] 0.000114102
FGA [NCBI] 0.000109886
F5 [NCBI] 9.49067e-05
F2 [NCBI] 7.37658e-05
TFPI [NCBI] 6.96914e-05
PROC [NCBI] 4.0157e-05
PF4 [NCBI] 3.74773e-05
PLG [NCBI] 3.65439e-05
FGG [NCBI] 3.60327e-05
CYP2C9 [NCBI] 3.15034e-05
SERPINC1 [NCBI] 2.38516e-05
KLKB1 [NCBI] 2.33953e-05
VKORC1 [NCBI] 2.21585e-05
GGCX [NCBI] 2.03714e-05
FGB [NCBI] 2.03569e-05
F7 [NCBI] 2.01287e-05
MTHFR [NCBI] 1.89143e-05
KNG1 [NCBI] 1.86167e-05
F12 [NCBI] 1.59144e-05
F8 [NCBI] 1.44482e-05
PROCR [NCBI] 1.39139e-05
SERPINE1 [NCBI] 1.30064e-05
F3 [NCBI] 1.2518e-05
MMRN1 [NCBI] 1.16914e-05
MET [NCBI] 1.03152e-05
P2RX1 [NCBI] 9.21839e-06
GP1BB [NCBI] 8.78742e-06
MCFD2 [NCBI] 8.78742e-06
CFI [NCBI] 7.91251e-06
F10 [NCBI] 7.50822e-06
KLK11 [NCBI] 7.33719e-06
CSTA [NCBI] 6.86652e-06
F11 [NCBI] 6.78625e-06
MMP8 [NCBI] 6.7475e-06
LMAN1 [NCBI] 6.56605e-06
PROS1 [NCBI] 6.46585e-06
CPB2 [NCBI] 6.31103e-06
ELA2 [NCBI] 6.22453e-06
RETNLB [NCBI] 6.03849e-06
THBD [NCBI] 5.89393e-06
GP1BA [NCBI] 5.59846e-06
SELP [NCBI] 5.39819e-06
FN1 [NCBI] 5.38113e-06
TFPI2 [NCBI] 5.25057e-06
ABCC6 [NCBI] 5.23495e-06
MMP7 [NCBI] 4.76466e-06
SELPLG [NCBI] 3.95386e-06
RETN [NCBI] 3.81834e-06
ITGB3 [NCBI] 3.57796e-06
PRKCA [NCBI] 3.31713e-06
PIH [NCBI] 3.02684e-06
TNF [NCBI] 2.89549e-06
ADAMTS13 [NCBI] 2.68828e-06
PTGS1 [NCBI] 2.08582e-06
CALCA [NCBI] 1.68174e-06
ACE [NCBI] 1.58033e-06
HRAS [NCBI] 1.47601e-06
NOS3 [NCBI] 1.20483e-06
HGF [NCBI] 9.91406e-07
APOE [NCBI] 4.02957e-07
PTH [NCBI] 1.3637e-07
EGFR [NCBI] 1.29568e-07



OMIM


 OMIM Link Information
gain		 01
scott syndrome [NCBI] 0.00539188
FGA [NCBI] 0.00148615
thrombasthenia-thrombocytopenia, hereditary [NCBI] 0.00078076
FGG [NCBI] 0.000710277
prekallikrein deficiency [NCBI] 0.000677273
storage pool platelet disease [NCBI] 0.000555363
F3 [NCBI] 0.000489025
F2 [NCBI] 0.000422113
GPS [NCBI] 0.000395833
giant platelet syndrome [NCBI] 0.000378648
PEE1 [NCBI] 0.00035536
F13A1 [NCBI] 0.000333636
flaujeac factor deficiency [NCBI] 0.000305365
factor xii deficiency [NCBI] 0.000298871
hemangioma-thrombocytopenia syndrome [NCBI] 0.000275353
protein c deficiency, congenital thrombotic disease due to [NCBI] 0.000245441
factor v deficiency [NCBI] 0.000233172
factor x deficiency [NCBI] 0.000225084
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 0.00022187
antithrombin iii deficiency [NCBI] 0.000215929
TFPI [NCBI] 0.000205401
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency [NCBI] 0.00019528
GGCX [NCBI] 0.000194082
thrombophilia due to deficiency of activated protein c cofactor [NCBI] 0.000171715
PLG [NCBI] 0.000152174
F5F8D [NCBI] 0.000133324
plasminogen deficiency, type i [NCBI] 0.000133324
thrombasthenia of glanzmann and naegeli [NCBI] 0.000127691
factor vii deficiency [NCBI] 0.00012768
NS1 [NCBI] 0.000123601
car factor deficiency [NCBI] 0.000113012
pechet factor deficiency [NCBI] 0.000113012
factor ix and factor xi, combined deficiency of [NCBI] 0.000113012
globulin anomaly involving beta (2a)-globulin [NCBI] 0.000113012
factor v excess with spontaneous thrombosis [NCBI] 0.000113012
glycogen storage disease ib [NCBI] 0.000107525
PF4 [NCBI] 0.000101065
TBXA2R [NCBI] 9.11581e-05
F8FD9 [NCBI] 9.05549e-05
factors viii, ix and xi, combined deficiency of [NCBI] 9.05549e-05
factor vii and factor viii, combined deficiency of [NCBI] 8.20878e-05
passovoy factor [NCBI] 8.20878e-05
athrombia, essential [NCBI] 8.20878e-05
bleeding disorder due to p2ry12 defect [NCBI] 7.65946e-05
PLAT [NCBI] 7.58001e-05
coumarin resistance [NCBI] 7.25138e-05
FHL2 [NCBI] 6.65655e-05
complement component c1q, fibroblast type [NCBI] 6.6336e-05
complement factor i deficiency [NCBI] 6.42569e-05
PAI1 [NCBI] 6.14286e-05
thrombocytopenic purpura, autoimmune [NCBI] 5.8462e-05
TMAU [NCBI] 5.60441e-05
HPS [NCBI] 5.54521e-05
CF [NCBI] 5.46281e-05
complement factor h deficiency [NCBI] 5.26008e-05
afibrinogenemia, congenital [NCBI] 5.16022e-05
THC2 [NCBI] 5.06632e-05
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome [NCBI] 4.8143e-05
P2RX1 [NCBI] 4.73789e-05
MADA [NCBI] 4.46801e-05
CPB2 [NCBI] 4.41411e-05
P2RY12 [NCBI] 4.15144e-05
F7R [NCBI] 3.95253e-05
COH1 [NCBI] 3.66559e-05
CMD1A [NCBI] 3.6294e-05
CDG1A [NCBI] 3.46058e-05
CLN3 [NCBI] 3.36783e-05
PTGS1 [NCBI] 3.31502e-05
FGB [NCBI] 3.22578e-05
FCMD [NCBI] 3.22518e-05
aHUS [NCBI] 3.22518e-05
porphyria, acute intermittent [NCBI] 3.12035e-05
F12 [NCBI] 2.999e-05
CFI [NCBI] 2.93393e-05
GP1BA [NCBI] 2.81576e-05
LPI [NCBI] 2.76419e-05
WRN [NCBI] 2.72538e-05
JMML [NCBI] 2.49664e-05
PTH [NCBI] 2.32874e-05
C3 [NCBI] 2.16225e-05
PROCR [NCBI] 2.1351e-05
fructose intolerance, hereditary [NCBI] 2.08312e-05
SLE [NCBI] 1.94455e-05
PCI [NCBI] 1.86067e-05
EGFR [NCBI] 1.8347e-05
FMF [NCBI] 1.67991e-05
TNF [NCBI] 1.62898e-05
PXE [NCBI] 1.21508e-05
CFH [NCBI] 1.20854e-05
homocystinuria [NCBI] 1.12403e-05
IFNA1 [NCBI] 9.73013e-06
WAS [NCBI] 8.66676e-06
hemophilia a [NCBI] 7.77499e-06
APOE [NCBI] 5.71771e-06
PI [NCBI] 4.23695e-06
HGF [NCBI] 2.76407e-06
XDH [NCBI] 1.75148e-06
CD [NCBI] 1.46633e-06



Database Center for Life Science