Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Vitamin K Deficiency [NCBI]

Gene


 Gene Link Information
Gain		 01
VKORC1 [NCBI] 0.000123052
MGP [NCBI] 7.41475e-05
AFP [NCBI] 2.66621e-05
GGCX [NCBI] 2.5473e-05
F7 [NCBI] 1.70889e-05
CYP2C9 [NCBI] 1.44893e-05
APOE [NCBI] 1.24281e-05
ARSE [NCBI] 1.1078e-05
PTH [NCBI] 5.78189e-06
TNFSF11 [NCBI] 4.44631e-06



OMIM


 OMIM Link Information
gain		 01
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 0.00043715
chondrodysplasia punctata, autosomal dominant [NCBI] 0.00018626
chondrodysplasia punctata, brachytelephalangic, autosomal [NCBI] 0.000118925
vitamin k-dependent clotting factors, combined deficiency of, 2 [NCBI] 0.000110446
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency [NCBI] 0.000110446
CF [NCBI] 0.000103839
coumarin resistance [NCBI] 0.000100846
AFP [NCBI] 9.37233e-05
VKORC1 [NCBI] 6.99095e-05
GGCX [NCBI] 6.14741e-05
BGLAP [NCBI] 3.71254e-05
APOE [NCBI] 3.50388e-05
PTH [NCBI] 2.27103e-05
CD [NCBI] 2.13794e-05



Database Center for Life Science