Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hernia, Inguinal [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science