Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Bladder Exstrophy [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 0.000189637
RP11-138L21.1 [NCBI] 2.04995e-05
CNTNAP3B [NCBI] 2.04995e-05
SET [NCBI] 1.23852e-05
FGF10 [NCBI] 1.22272e-05
MYH9 [NCBI] 1.11047e-05
NPY [NCBI] 6.16477e-06
EGF [NCBI] 4.44657e-06



OMIM


 OMIM Link Information
gain		 01
exstrophy of bladder [NCBI] 0.00669356
oeis complex [NCBI] 0.00105971
aplasia cutis congenita with epibulbar dermoids [NCBI] 0.000106243
opitz syndrome [NCBI] 9.73745e-05
NR5A1 [NCBI] 6.36001e-05
NPY [NCBI] 2.30259e-05
KLK3 [NCBI] 1.39638e-05
EGF [NCBI] 1.35784e-05



Database Center for Life Science