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01 Malabsorption Syndromes [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC5A1 [NCBI] 0.000178917
CUBN [NCBI] 0.000102031
SLC46A1 [NCBI] 4.07892e-05
SI [NCBI] 2.97743e-05
SAR1B [NCBI] 2.47405e-05
PTH [NCBI] 2.44878e-05
SLC10A2 [NCBI] 2.29765e-05
SLC39A4 [NCBI] 2.11514e-05
PYY [NCBI] 2.09613e-05
NEUROG3 [NCBI] 2.01133e-05
FOLR1 [NCBI] 1.738e-05
BAAT [NCBI] 1.3574e-05
HSD3B7 [NCBI] 1.26757e-05
GIF [NCBI] 1.10256e-05
SAR1A [NCBI] 1.10256e-05
AMN [NCBI] 1.07796e-05
SLC2A1 [NCBI] 1.00109e-05
TJP2 [NCBI] 9.77037e-06
FGF19 [NCBI] 9.32521e-06
ACADVL [NCBI] 9.32521e-06
PPYR1 [NCBI] 9.13966e-06
APOB [NCBI] 8.73391e-06
SLC5A3 [NCBI] 8.55051e-06
SLC15A1 [NCBI] 8.48933e-06
TRPM6 [NCBI] 8.48933e-06
APOA2 [NCBI] 8.21253e-06
DPP7 [NCBI] 8.11326e-06
DES [NCBI] 7.8053e-06
SBDS [NCBI] 7.72665e-06
CFTR [NCBI] 7.50561e-06
APOA4 [NCBI] 7.34905e-06
NEUROD1 [NCBI] 7.09241e-06
FABP1 [NCBI] 6.98971e-06
PRSS2 [NCBI] 6.47769e-06
FABP2 [NCBI] 6.40562e-06
PRSS1 [NCBI] 6.08534e-06
CYP27A1 [NCBI] 5.66226e-06
APOA1 [NCBI] 5.19168e-06
GIP [NCBI] 4.69432e-06
SLC11A1 [NCBI] 4.39012e-06
VIP [NCBI] 2.61052e-06
VDR [NCBI] 2.54454e-06
CCK [NCBI] 2.41396e-06
NPY [NCBI] 1.85041e-06
PCNA [NCBI] 1.09607e-06



OMIM


 OMIM Link Information
gain		 01
folic acid, transport defect involving [NCBI] 0.00355151
GGM [NCBI] 0.000926257
megaloblastic anemia 1 [NCBI] 0.000760754
histidinuria due to a renal tubular defect [NCBI] 0.000744944
methionine malabsorption syndrome [NCBI] 0.000744944
cholestasis-lymphedema syndrome [NCBI] 0.000673834
diarrhea 2, with microvillous atrophy [NCBI] 0.000572697
CSID [NCBI] 0.000531537
CMRD [NCBI] 0.000456622
SLC5A1 [NCBI] 0.000443586
ATD1 [NCBI] 0.000384555
anderson disease [NCBI] 0.000371722
CD [NCBI] 0.000344374
JBS [NCBI] 0.000343637
SLC10A2 [NCBI] 0.000340358
CUBN [NCBI] 0.000306884
ABL [NCBI] 0.000263075
AEZ [NCBI] 0.00025308
CF [NCBI] 0.000147656
SLE [NCBI] 0.000136396
SI [NCBI] 0.000131013
diarrhea 4, malabsorptive, congenital [NCBI] 0.00010818
lysine malabsorption syndrome [NCBI] 0.00010818
diarrhea, glucose-stimulated secretory, with common variable immunodeficiency [NCBI] 0.00010818
bile acid, synthetic defect of [NCBI] 0.00010818
lactase persistence [NCBI] 9.58344e-05
FHCA [NCBI] 8.57276e-05
PYY [NCBI] 8.13851e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 8.0717e-05
BAAT [NCBI] 7.82236e-05
bile acid synthesis defect, congenital, 1 [NCBI] 6.77024e-05
pernicious anemia [NCBI] 6.77024e-05
anemia, microcytic [NCBI] 6.44587e-05
SAR1A [NCBI] 6.44466e-05
TJP2 [NCBI] 6.44466e-05
SDS [NCBI] 6.24687e-05
enterokinase deficiency [NCBI] 6.17647e-05
PG [NCBI] 6.05445e-05
HSD3B7 [NCBI] 5.92489e-05
TREH [NCBI] 5.92489e-05
SAR1B [NCBI] 5.92489e-05
APS1 [NCBI] 5.83576e-05
PTH [NCBI] 5.59148e-05
NEUROG3 [NCBI] 5.58748e-05
GLYS1 [NCBI] 5.56657e-05
IFD [NCBI] 5.40623e-05
lipase, congenital absence of pancreatic [NCBI] 5.33669e-05
CVID [NCBI] 5.2914e-05
HOMG [NCBI] 5.1275e-05
HOMG3 [NCBI] 5.00472e-05
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 5.00472e-05
SIL1 [NCBI] 4.97082e-05
SLC39A4 [NCBI] 4.97082e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 4.78476e-05
H6PD [NCBI] 4.495e-05
FBS [NCBI] 4.42067e-05
hartnup disorder [NCBI] 4.42067e-05
IGKC [NCBI] 4.04773e-05
myopathy, myofibrillar, desmin-related [NCBI] 3.93766e-05
PRSS1 [NCBI] 3.69874e-05
MSS [NCBI] 3.66765e-05
immunodeficiency-centromeric instability-facial anomalies syndrome [NCBI] 3.57194e-05
PFIC1 [NCBI] 3.5263e-05
FIH [NCBI] 3.43902e-05
DES [NCBI] 3.29314e-05
SLC2A2 [NCBI] 3.2659e-05
wolman disease [NCBI] 3.09412e-05
HHF2 [NCBI] 2.69381e-05
APOB [NCBI] 2.66641e-05
LPI [NCBI] 2.32114e-05
CGD [NCBI] 2.21099e-05
SPINK1 [NCBI] 1.87e-05
CCK [NCBI] 1.55508e-05
GIP [NCBI] 1.39329e-05
TTR [NCBI] 7.21108e-06
VDR [NCBI] 4.97193e-06
VIP [NCBI] 3.71755e-06
CFTR [NCBI] 2.80258e-06
NPY [NCBI] 1.10362e-06
PCNA [NCBI] 1.53558e-09



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