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01 Intestinal Obstruction [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000158688
CFTR [NCBI] 0.000130084
VIP [NCBI] 2.9424e-05
NOD2 [NCBI] 1.65678e-05
CX3CR1 [NCBI] 1.53303e-05
CALCA [NCBI] 1.47513e-05
MPO [NCBI] 1.04731e-05
CANX [NCBI] 9.89781e-06
GAL [NCBI] 9.39216e-06
SLC1A5 [NCBI] 8.94519e-06
DES [NCBI] 8.37678e-06
EDNRB [NCBI] 7.74434e-06
MSH2 [NCBI] 7.70468e-06
XDH [NCBI] 7.66289e-06
ACHE [NCBI] 7.59501e-06
KLF4 [NCBI] 7.24226e-06
CX3CL1 [NCBI] 6.3962e-06
SPAST [NCBI] 6.3962e-06
MSH3 [NCBI] 6.33453e-06
CDX2 [NCBI] 5.87165e-06
GDNF [NCBI] 4.89723e-06
MSH6 [NCBI] 4.85681e-06
KRT7 [NCBI] 4.62888e-06
KRT20 [NCBI] 4.2613e-06
PTGS2 [NCBI] 4.00116e-06
RET [NCBI] 3.9169e-06
CCK [NCBI] 2.93878e-06
IL6 [NCBI] 2.64625e-06
CD68 [NCBI] 2.52122e-06
TNF [NCBI] 1.95399e-06
VWF [NCBI] 1.84611e-06



OMIM


 OMIM Link Information
gain		 01
megaduodenum and/or megacystis [NCBI] 0.00970204
volvulus of midgut [NCBI] 0.00274066
visceral neuropathy, familial, autosomal recessive [NCBI] 0.00269606
CF [NCBI] 0.00187867
jejunal atresia [NCBI] 0.00173084
CFM1 [NCBI] 0.00152161
visceral myopathy, familial, with external ophthalmoplegia [NCBI] 0.00122277
intestinal atresia, multiple [NCBI] 0.000948967
visceral neuropathy, familial, autosomal dominant [NCBI] 0.000555675
basal ganglia calcification, idiopathic, childhood-onset [NCBI] 0.000385833
megacystis-microcolon-intestinal hypoperistalsis syndrome [NCBI] 0.00034774
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000155525
HSCR1 [NCBI] 0.000144921
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked [NCBI] 0.000144576
CFTR [NCBI] 0.00013212
SLE [NCBI] 0.000131039
intestinal pseudoobstruction with patent ductus arteriosus and natal teeth [NCBI] 0.000108618
duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery [NCBI] 0.000108618
VIP [NCBI] 0.0001079
GUCY1B3 [NCBI] 8.26658e-05
splenogonadal fusion with limb defects and micrognathia [NCBI] 6.81384e-05
jejunal atresia with microcephaly and ocular anomalies [NCBI] 6.81384e-05
CRC [NCBI] 6.75974e-05
CGD [NCBI] 6.61609e-05
pelvis-shoulder dysplasia [NCBI] 6.48942e-05
pancreas, annular [NCBI] 6.21996e-05
SLC1A5 [NCBI] 6.03129e-05
FMF [NCBI] 5.48884e-05
waardenburg-shah syndrome [NCBI] 4.63494e-05
DMD [NCBI] 4.18117e-05
XDH [NCBI] 4.09516e-05
epidermolysis bullosa with pyloric atresia [NCBI] 3.98005e-05
RP3 [NCBI] 3.76008e-05
DES [NCBI] 3.73256e-05
autonomic control, congenital failure of [NCBI] 3.70977e-05
PJS [NCBI] 3.70124e-05
SGBS1 [NCBI] 3.61395e-05
wolman disease [NCBI] 3.53245e-05
RP2 [NCBI] 3.44596e-05
FDH [NCBI] 3.17549e-05
GIST [NCBI] 2.71226e-05
WS1 [NCBI] 2.70937e-05
MPO [NCBI] 2.66298e-05
GAL [NCBI] 2.60442e-05
ABP1 [NCBI] 2.59586e-05
DMD [NCBI] 2.0946e-05
ACHE [NCBI] 2.01843e-05
CRH [NCBI] 1.82405e-05
NF1 [NCBI] 1.59946e-05
GDNF [NCBI] 1.18641e-05
CCK [NCBI] 5.83255e-06
CEACAM5 [NCBI] 3.91761e-06
AVP [NCBI] 2.71913e-06
VEGF [NCBI] 2.70024e-06
temporal arteritis [NCBI] 2.10092e-06
APC [NCBI] 1.60656e-06
TNF [NCBI] 2.69112e-07



Database Center for Life Science