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01 Esophageal Atresia [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.00666007
HFM [NCBI] 8.47743e-05
SHH [NCBI] 4.90658e-05
SOX2 [NCBI] 4.85508e-05
MYCN [NCBI] 1.71401e-05
NKX2-1 [NCBI] 1.58543e-05
SIX2 [NCBI] 1.46475e-05
SLC17A5 [NCBI] 1.16928e-05
GLI2 [NCBI] 1.00941e-05
HOXD13 [NCBI] 9.929e-06
SMO [NCBI] 9.83709e-06
GLI3 [NCBI] 9.17696e-06
GLI1 [NCBI] 9.09768e-06
NOG [NCBI] 8.26962e-06
BMP7 [NCBI] 7.11739e-06
VIP [NCBI] 5.04933e-06
NPY [NCBI] 4.21356e-06
AFP [NCBI] 3.51891e-06



OMIM


 OMIM Link Information
gain		 01
tracheoesophageal fistula with or without esophageal atresia [NCBI] 0.00104166
feingold syndrome [NCBI] 0.000741448
MCOPS3 [NCBI] 0.000722758
thrombocytopenia-absent radius syndrome [NCBI] 0.000679776
HFM [NCBI] 0.000529988
SHH [NCBI] 0.000254265
vacterl association with hydrocephalus [NCBI] 0.000184233
SOX2 [NCBI] 0.000121277
gastrointestinal abnormalities, multiple [NCBI] 9.73662e-05
acrorenal-mandibular syndrome [NCBI] 8.77736e-05
vacterl association with hydrocephalus, x-linked [NCBI] 7.7463e-05
vater association [NCBI] 7.4046e-05
ITGA6 [NCBI] 7.13032e-05
FMD [NCBI] 6.58021e-05
UMS [NCBI] 6.40591e-05
FANCB [NCBI] 6.17519e-05
infantile sialic acid storage disorder [NCBI] 5.91268e-05
ABS [NCBI] 5.74056e-05
MKKS [NCBI] 5.6871e-05
ITGB4 [NCBI] 5.44865e-05
SLC17A5 [NCBI] 5.44865e-05
MYCN [NCBI] 5.03403e-05
DGS [NCBI] 2.88396e-05
GDNF [NCBI] 1.88087e-05
MUC1 [NCBI] 1.53883e-05
VIP [NCBI] 1.32332e-05
FA [NCBI] 1.24173e-05
NPY [NCBI] 8.97515e-06
AFP [NCBI] 5.83198e-06



Database Center for Life Science