Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Aminopyrine [NCBI]

Gene


 Gene Link Information
Gain		 01
EGF [NCBI] 1.73842e-05
CCK [NCBI] 4.58579e-06
CYP2C19 [NCBI] 4.26426e-06
CYP1A2 [NCBI] 3.23767e-06
CYP2C9 [NCBI] 2.56989e-06
KCNE2 [NCBI] 1.86329e-06
CTSA [NCBI] 1.66416e-06
LPO [NCBI] 1.61524e-06
PTGER1 [NCBI] 1.48888e-06
CYP2C8 [NCBI] 1.4663e-06
RAB11A [NCBI] 1.44187e-06
CYP2E1 [NCBI] 1.42703e-06
ADCYAP1 [NCBI] 1.3706e-06
GIP [NCBI] 1.27231e-06
NOS3 [NCBI] 9.01387e-07
NOS2 [NCBI] 8.88987e-07
VIP [NCBI] 7.88244e-07



OMIM


 OMIM Link Information
gain		 01
gilbert syndrome [NCBI] 0.000184253
EGF [NCBI] 0.000148955
CCK [NCBI] 3.42315e-05
LPO [NCBI] 1.7697e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 1.62111e-05
GIP [NCBI] 1.09899e-05
ADCYAP1 [NCBI] 9.39287e-06
FRAP1 [NCBI] 9.36624e-06
VIP [NCBI] 2.50216e-06
CRH [NCBI] 2.30156e-06



Database Center for Life Science