Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Infant Nutritional Physiological Phenomena	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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