Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Fetal Macrosomia	[NCBI]

Gene	Link	Information Gain
H19	[NCBI]	0.000312204
KCNQ1OT1	[NCBI]	0.00030326
HNF4A	[NCBI]	3.82543e-05
GPC3	[NCBI]	3.14985e-05
PGM1	[NCBI]	2.46827e-05
PIH	[NCBI]	2.31094e-05
SLC2A3	[NCBI]	2.04917e-05
SLC2A4	[NCBI]	1.48882e-05
INS	[NCBI]	1.42707e-05
HNF1A	[NCBI]	1.41631e-05
LGALS13	[NCBI]	1.1744e-05
IGFBP1	[NCBI]	7.45561e-06
IGF2	[NCBI]	6.58161e-06
FLT1	[NCBI]	6.50313e-06
IGFBP3	[NCBI]	6.46522e-06
EGF	[NCBI]	6.06859e-06
AHR	[NCBI]	6.06645e-06
LEP	[NCBI]	5.7403e-06
SLC2A1	[NCBI]	5.63413e-06
IGF1	[NCBI]	5.58532e-06
AFP	[NCBI]	2.85024e-06
VEGFA	[NCBI]	2.80114e-06

OMIM	Link	Information gain
renal hamartomas, nephroblastomatosis, and fetal gigantism	[NCBI]	0.00108068
weaver syndrome	[NCBI]	0.000289042
megalencephaly-cutis marmorata telangiectatica congenita	[NCBI]	0.000204428
macrosomia with microphthalmia, lethal	[NCBI]	0.000143802
preaxial hallucal polydactyly	[NCBI]	0.000143802
clark-baraitser syndrome	[NCBI]	9.99902e-05
BWS	[NCBI]	9.32348e-05
SGBS1	[NCBI]	7.07404e-05
GRB10	[NCBI]	6.53402e-05
sotos syndrome	[NCBI]	6.26044e-05
PGM1	[NCBI]	6.15648e-05
HHF2	[NCBI]	6.14849e-05
LQT1	[NCBI]	5.89884e-05
KCNQ1OT1	[NCBI]	5.73625e-05
CDKN1C	[NCBI]	5.49429e-05
H19	[NCBI]	5.29997e-05
IGF2	[NCBI]	5.0312e-05
GPC3	[NCBI]	4.99813e-05
MODY	[NCBI]	4.09635e-05
INS	[NCBI]	3.1054e-05
LCAT	[NCBI]	2.9942e-05
PI	[NCBI]	2.86475e-05
AHR	[NCBI]	2.73465e-05
EGF	[NCBI]	1.93194e-05
AFP	[NCBI]	8.6171e-06
VEGF	[NCBI]	9.48402e-07