Gendoo

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01 Digestive System Abnormalities [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000158688
FGF10 [NCBI] 2.32037e-05
SHH [NCBI] 1.63488e-05
FOXL1 [NCBI] 1.47485e-05
ACHE [NCBI] 1.17353e-05
GAL [NCBI] 1.14735e-05
HOXA13 [NCBI] 1.08145e-05
ITGB4 [NCBI] 9.68863e-06
AFP [NCBI] 9.63567e-06
NOG [NCBI] 8.3704e-06
JAG1 [NCBI] 7.8411e-06
MYCN [NCBI] 7.43092e-06
BMP7 [NCBI] 7.21788e-06
VIP [NCBI] 5.14846e-06
AR [NCBI] 3.75719e-06



OMIM


 OMIM Link Information
gain		 01
intestinal atresia, multiple [NCBI] 0.00279952
thrombocytopenia-absent radius syndrome [NCBI] 0.000545114
gastrointestinal abnormalities, multiple [NCBI] 0.000412382
CDLS1 [NCBI] 0.000186566
MYO1D [NCBI] 0.000183847
cardiofaciocutaneous syndrome [NCBI] 0.000144621
craniomicromelic syndrome [NCBI] 0.000114122
jejunal atresia with microcephaly and ocular anomalies [NCBI] 9.6046e-05
cleft larynx, posterior [NCBI] 9.27854e-05
pancreas, annular [NCBI] 9.00744e-05
rokitansky-kuster-hauser syndrome [NCBI] 8.77542e-05
gastroschisis [NCBI] 8.77542e-05
epidermolysis bullosa with pyloric atresia [NCBI] 6.73472e-05
SHH [NCBI] 6.28645e-05
TBS [NCBI] 6.21912e-05
apert syndrome [NCBI] 6.21912e-05
FGF10 [NCBI] 6.03671e-05
CES [NCBI] 5.66621e-05
ITGB4 [NCBI] 5.57696e-05
GDNF [NCBI] 5.40242e-05
ACHE [NCBI] 3.65587e-05
GAL [NCBI] 3.47854e-05
BWS [NCBI] 2.82425e-05
AFP [NCBI] 2.56687e-05
PWS [NCBI] 1.69841e-05
VIP [NCBI] 1.43877e-05
AR [NCBI] 8.87801e-06



Database Center for Life Science