Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypoprothrombinemias [NCBI]

Gene


 Gene Link Information
Gain		 01
F2 [NCBI] 9.15672e-05
VKORC1 [NCBI] 3.27244e-05
GGCX [NCBI] 2.73408e-05
F10 [NCBI] 1.0946e-05
ATP8B1 [NCBI] 1.0106e-05
TPMT [NCBI] 9.12275e-06
TTR [NCBI] 5.94674e-06
F5 [NCBI] 5.603e-06
PTGS2 [NCBI] 2.60775e-06



OMIM


 OMIM Link Information
gain		 01
factor x deficiency [NCBI] 0.00130991
scott syndrome [NCBI] 0.0010375
F2 [NCBI] 0.000962934
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 0.00072148
F8FD9 [NCBI] 0.000120084
factor vii and factor viii, combined deficiency of [NCBI] 0.000111604
hyperpipecolatemia [NCBI] 9.37095e-05
F5F8D [NCBI] 8.4187e-05
factor vii deficiency [NCBI] 8.06276e-05
PFIC1 [NCBI] 6.90237e-05
PGL1 [NCBI] 6.52872e-05
GGCX [NCBI] 4.8574e-05
ATP8B1 [NCBI] 4.76717e-05
SLE [NCBI] 4.24705e-05
TPMT [NCBI] 3.36627e-05
antithrombin iii deficiency [NCBI] 2.66442e-05
TTR [NCBI] 1.01699e-05



Database Center for Life Science