Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Esophageal Atresia	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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