Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hernia, Inguinal	[NCBI]

Gene	Link	Information Gain
AIR	[NCBI]	0.000209298
VUR	[NCBI]	0.000129473
MMP13	[NCBI]	2.53835e-05
INSL3	[NCBI]	1.95093e-05
PTGS2	[NCBI]	1.86616e-05
AMH	[NCBI]	1.824e-05
ATP2B1	[NCBI]	1.18928e-05
MED12	[NCBI]	1.10157e-05
ATP2A1	[NCBI]	1.08009e-05
FGD1	[NCBI]	1.06713e-05
HGF	[NCBI]	9.80404e-06
TIMP2	[NCBI]	8.34982e-06
CNN1	[NCBI]	7.76937e-06
CD68	[NCBI]	3.9768e-06
NOS2	[NCBI]	3.775e-06
CTNNB1	[NCBI]	3.47702e-06
BAX	[NCBI]	3.3017e-06
AR	[NCBI]	3.25138e-06
FASLG	[NCBI]	3.20123e-06
PRL	[NCBI]	2.94962e-06

OMIM	Link	Information gain
oculocerebral syndrome with hypopigmentation	[NCBI]	0.000817902
robinow syndrome, autosomal dominant	[NCBI]	0.000676229
SPS	[NCBI]	0.000522538
PMDS	[NCBI]	0.000294246
lambert syndrome	[NCBI]	0.000265132
faciogenital dysplasia	[NCBI]	0.000145045
SCDO1	[NCBI]	0.000142961
microspherophakia with hernia	[NCBI]	0.000132242
acrocephalopolysyndactyly type iii	[NCBI]	0.000132242
AIS	[NCBI]	8.8137e-05
spondylocarpotarsal synostosis syndrome	[NCBI]	8.57315e-05
AMH	[NCBI]	8.55965e-05
gastroschisis	[NCBI]	8.34124e-05
serpentine fibula-polycystic kidney syndrome	[NCBI]	8.13853e-05
IHPS1	[NCBI]	7.27487e-05
UMS	[NCBI]	6.79674e-05
CBAVD	[NCBI]	6.7161e-05
hyperekplexia, hereditary	[NCBI]	6.56608e-05
frank-ter haar syndrome	[NCBI]	6.48204e-05
PPS	[NCBI]	6.42893e-05
FGD1	[NCBI]	6.24692e-05
GCPS	[NCBI]	5.47049e-05
ANG	[NCBI]	4.75941e-05
HGF	[NCBI]	3.96583e-05
SLOS	[NCBI]	2.95637e-05
polycystic kidneys	[NCBI]	2.1337e-05
SLE	[NCBI]	1.75524e-05
PRL	[NCBI]	8.1404e-06
CEACAM5	[NCBI]	5.06577e-06
KLK3	[NCBI]	5.00333e-06
CF	[NCBI]	4.11183e-06
VEGF	[NCBI]	1.31341e-06