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MeSH keywords -> Related genes, diseases (OMIM)


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01 Infant Nutritional Physiological Phenomena [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 6.60387e-05
MS [NCBI] 2.45164e-05
PTH [NCBI] 7.30024e-06
GIP [NCBI] 5.19407e-06
LALBA [NCBI] 3.41242e-06
WFDC5 [NCBI] 2.46413e-06
GHRL [NCBI] 2.36909e-06
EGF [NCBI] 2.25262e-06
LEP [NCBI] 2.12381e-06
INS [NCBI] 2.08963e-06
IGF1 [NCBI] 2.02342e-06
TTR [NCBI] 1.98702e-06
FOLR1 [NCBI] 1.97898e-06
PTPN11 [NCBI] 1.91611e-06
LPL [NCBI] 1.50363e-06
HGF [NCBI] 1.46005e-06
VIP [NCBI] 1.41324e-06
EPO [NCBI] 1.34742e-06
APOE [NCBI] 1.2997e-06
PRL [NCBI] 1.13679e-06



OMIM


 OMIM Link Information
gain		 01
CF [NCBI] 0.000174674
hyperlipoproteinemia, type i [NCBI] 0.000110428
CEL [NCBI] 5.9748e-05
CD [NCBI] 4.10493e-05
GIP [NCBI] 3.79835e-05
PTH [NCBI] 3.54107e-05
fructose intolerance, hereditary [NCBI] 2.91512e-05
SLC40A1 [NCBI] 2.91512e-05
phenylketonuria [NCBI] 1.76186e-05
hla-d histocompatibility type [NCBI] 1.23093e-05
RNASE3 [NCBI] 1.07665e-05
TTR [NCBI] 1.07592e-05
LPL [NCBI] 5.6196e-06
HGF [NCBI] 4.90604e-06
APOE [NCBI] 4.78929e-06
VIP [NCBI] 4.06719e-06
EGF [NCBI] 3.28698e-06
PRL [NCBI] 1.71514e-06



Database Center for Life Science