Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Intestinal Perforation [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 0.000189637
COL3A1 [NCBI] 2.02629e-05
PTGS2 [NCBI] 1.40762e-05
PTX3 [NCBI] 9.23776e-06
ABCC2 [NCBI] 7.89444e-06
SELPLG [NCBI] 7.53734e-06
NOD2 [NCBI] 5.68313e-06
CCL2 [NCBI] 5.56978e-06
TNF [NCBI] 5.52965e-06
APC [NCBI] 5.10992e-06
NOS2 [NCBI] 4.28821e-06
MPO [NCBI] 3.64768e-06
VEGFA [NCBI] 3.56446e-06
CFTR [NCBI] 3.19201e-06



OMIM


 OMIM Link Information
gain		 01
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 0.000133758
SLE [NCBI] 8.00292e-05
CRC [NCBI] 6.82297e-05
ehlers-danlos syndrome, type vi [NCBI] 6.24992e-05
ehlers-danlos syndrome, type i [NCBI] 5.56645e-05
COL3A1 [NCBI] 4.94215e-05
IBD1 [NCBI] 4.43059e-05
VEGF [NCBI] 3.77678e-05
fabry disease [NCBI] 3.74262e-05
GIST [NCBI] 2.25593e-05
polycystic kidneys [NCBI] 1.97435e-05
TNF [NCBI] 1.89009e-05
FMF [NCBI] 1.29924e-05
MPO [NCBI] 1.25029e-05
CEACAM5 [NCBI] 7.56857e-06
RA [NCBI] 7.0689e-07
CF [NCBI] 2.23454e-08



Database Center for Life Science