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01 Hernia, Diaphragmatic [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.00188244
DIH1 [NCBI] 0.000668676
THAS [NCBI] 0.000332969
NKX2-1 [NCBI] 4.96166e-05
ZFPM2 [NCBI] 3.97719e-05
TRH [NCBI] 2.30016e-05
SCGB1A1 [NCBI] 1.34478e-05
SHH [NCBI] 1.28916e-05
STRA6 [NCBI] 1.2611e-05
FGF18 [NCBI] 1.17319e-05
AGT [NCBI] 1.10801e-05
NR2F2 [NCBI] 1.02768e-05
THRA [NCBI] 1.00053e-05
LRP2 [NCBI] 1.00053e-05
TNKS [NCBI] 9.63088e-06
MEF2A [NCBI] 9.44013e-06
EFNB1 [NCBI] 9.44013e-06
AQP5 [NCBI] 9.16299e-06
FGF10 [NCBI] 8.6383e-06
EGF [NCBI] 8.58055e-06
GATA4 [NCBI] 8.45971e-06
SMO [NCBI] 8.23742e-06
NOS3 [NCBI] 8.0432e-06
RARB [NCBI] 7.98852e-06
GLI1 [NCBI] 7.49972e-06
PDGFRA [NCBI] 7.19953e-06
TIMP2 [NCBI] 7.18342e-06
NRG1 [NCBI] 6.87626e-06
NPPB [NCBI] 6.69862e-06
NR3C1 [NCBI] 6.52696e-06
MPO [NCBI] 6.36047e-06
GHRL [NCBI] 5.99083e-06
PAX3 [NCBI] 5.83955e-06
ADM [NCBI] 5.80377e-06
MMP1 [NCBI] 5.71417e-06
PAX6 [NCBI] 5.42527e-06
PDE5A [NCBI] 5.28985e-06
AGTR1 [NCBI] 5.28466e-06
HMOX1 [NCBI] 4.72671e-06
ACE [NCBI] 3.31498e-06
NOS2 [NCBI] 2.67535e-06
AR [NCBI] 2.17881e-06
TNF [NCBI] 4.41153e-07



OMIM


 OMIM Link Information
gain		 01
diaphragmatic hernia, congenital [NCBI] 0.012596
FRNS [NCBI] 0.00889681
hernia, hiatus [NCBI] 0.00218225
DIH2 [NCBI] 0.00138693
kabuki syndrome [NCBI] 0.00074958
MCOPS9 [NCBI] 0.000486319
donnai-barrow syndrome [NCBI] 0.000409162
hypertelorism, teebi type [NCBI] 0.000394467
diaphragmatic hernia 3 [NCBI] 0.000364472
microcephaly, hiatus hernia, and nephrotic syndrome [NCBI] 0.000353703
renal hamartomas, nephroblastomatosis, and fetal gigantism [NCBI] 0.000336936
THAS [NCBI] 0.000336936
gastroesophageal reflux [NCBI] 0.000264359
anencephaly [NCBI] 0.000255266
hernia, anterior diaphragmatic [NCBI] 0.000242653
SGBS1 [NCBI] 0.000200257
ehlers-danlos syndrome, type i [NCBI] 0.000194644
LRP2 [NCBI] 0.000173009
WHS [NCBI] 0.000151477
CDLS1 [NCBI] 0.000139301
NR2F2 [NCBI] 0.000138635
CFNS [NCBI] 0.000123789
alport syndrome, autosomal dominant [NCBI] 0.000122838
gastrocutaneous syndrome [NCBI] 0.000121164
esophageal ring, lower [NCBI] 0.000121164
epidermolysis bullosa with diaphragmatic hernia [NCBI] 0.000121164
SCDO1 [NCBI] 0.000120623
PKS [NCBI] 0.000120623
FDH [NCBI] 0.000110403
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000102234
meacham syndrome [NCBI] 9.87009e-05
sucrosuria, hiatus hernia and mental retardation [NCBI] 9.87009e-05
omphalocele, diaphragmatic hernia, and radial ray defects [NCBI] 9.02278e-05
MSC [NCBI] 8.29498e-05
SLIT3 [NCBI] 8.29498e-05
MLRD [NCBI] 8.06418e-05
malpuech facial clefting syndrome [NCBI] 8.06418e-05
cleft lip/palate with abnormal thumbs and microcephaly [NCBI] 7.73868e-05
pancreatic agenesis, congenital [NCBI] 7.23669e-05
TCF21 [NCBI] 6.39723e-05
STRA6 [NCBI] 6.39723e-05
FGF18 [NCBI] 6.39723e-05
VEGF [NCBI] 6.13792e-05
denys-drash syndrome [NCBI] 6.06627e-05
GJA1 [NCBI] 5.87139e-05
cutis laxa, autosomal recessive, type i [NCBI] 5.61748e-05
ZFPM2 [NCBI] 5.44259e-05
FGF7 [NCBI] 5.30914e-05
AQP5 [NCBI] 5.30032e-05
FTH1 [NCBI] 5.30032e-05
PHA [NCBI] 5.26817e-05
donohue syndrome [NCBI] 5.20672e-05
FGF10 [NCBI] 5.17597e-05
PDGFRA [NCBI] 4.64608e-05
COH1 [NCBI] 4.45552e-05
BPES [NCBI] 4.03473e-05
REN [NCBI] 3.87864e-05
WT1 [NCBI] 3.35719e-05
PAX6 [NCBI] 3.26953e-05
ADM [NCBI] 2.30201e-05
CPI [NCBI] 2.07059e-05
SHH [NCBI] 1.61721e-05
EGF [NCBI] 1.28772e-05
MPO [NCBI] 1.16917e-05
FA [NCBI] 7.1679e-06
AR [NCBI] 2.73303e-06
TNF [NCBI] 1.54248e-06
MG [NCBI] 1.09213e-07



Database Center for Life Science