Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Factor IXa [NCBI]

Gene


 Gene Link Information
Gain		 01
EPR1 [NCBI] 0.000151102
NEWENTRY [NCBI] 0.00010396
F9 [NCBI] 7.0851e-05
F8 [NCBI] 3.24598e-05
F10 [NCBI] 2.1136e-05
EGF [NCBI] 1.30718e-05
F11 [NCBI] 3.54075e-06
F7 [NCBI] 3.04608e-06
VWF [NCBI] 2.74238e-06
TFPI [NCBI] 2.45172e-06
SERPINA10 [NCBI] 1.88105e-06
LCN1 [NCBI] 1.55866e-06
PROS1 [NCBI] 1.55064e-06
THBD [NCBI] 1.51152e-06
SERPINC1 [NCBI] 1.47942e-06
LRP1 [NCBI] 1.40895e-06
PROC [NCBI] 1.38245e-06
F3 [NCBI] 1.33624e-06
F2 [NCBI] 1.03215e-06
TF [NCBI] 9.32972e-07
TNF [NCBI] 2.88527e-07



OMIM


 OMIM Link Information
gain		 01
scott syndrome [NCBI] 0.00207901
thrombophilia due to deficiency of activated protein c cofactor [NCBI] 0.000186123
F3 [NCBI] 0.00016086
HEMB [NCBI] 0.000119743
EGF [NCBI] 0.000107328
thrombocytopenic purpura, autoimmune [NCBI] 6.64104e-05
LRP1 [NCBI] 5.30749e-05
TFPI [NCBI] 2.40068e-05
factor v deficiency [NCBI] 1.94482e-05
APP [NCBI] 1.49435e-05
PI [NCBI] 1.23002e-05
TNF [NCBI] 2.94329e-07



Database Center for Life Science