Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Fetal Macrosomia [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science