Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Urinary Incontinence [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 0.000721932
MS [NCBI] 0.000686378
TRPV1 [NCBI] 2.9899e-05
NGF [NCBI] 2.96452e-05
SMTN [NCBI] 1.2828e-05
P2RX1 [NCBI] 1.22498e-05
LIG1 [NCBI] 1.11009e-05
SCNN1G [NCBI] 1.07949e-05
FAT1 [NCBI] 1.07263e-05
SCNN1A [NCBI] 1.05354e-05
SLC18A3 [NCBI] 1.01109e-05
SCNN1B [NCBI] 9.18852e-06
KCNJ8 [NCBI] 8.15136e-06
MPZ [NCBI] 8.15136e-06
HTR2A [NCBI] 7.76505e-06
XRCC3 [NCBI] 7.55243e-06
OPRL1 [NCBI] 7.46028e-06
UGT1A1 [NCBI] 6.4042e-06
SHBG [NCBI] 5.25428e-06
SNCA [NCBI] 4.63575e-06
TRH [NCBI] 4.43118e-06
ACE [NCBI] 4.36573e-06



OMIM


 OMIM Link Information
gain		 01
camptobrachydactyly [NCBI] 0.00129156
pelvic organ prolapse [NCBI] 0.00107364
KLK3 [NCBI] 0.000314634
sacral defect with anterior meningocele [NCBI] 0.000167554
MDD [NCBI] 0.000104701
ureterocele [NCBI] 0.000103324
charcot-marie-tooth disease, axonal, type 2j [NCBI] 9.04679e-05
spinal muscular atrophy, proximal, adult, autosomal dominant [NCBI] 8.34102e-05
NGFB [NCBI] 8.09794e-05
apnea, obstructive sleep [NCBI] 7.89651e-05
SMA3 [NCBI] 6.03371e-05
ADHD [NCBI] 5.50039e-05
SCA7 [NCBI] 5.28878e-05
glycogen storage disease ii [NCBI] 4.52129e-05
SCA1 [NCBI] 4.38862e-05
MPZ [NCBI] 3.12245e-05
von willebrand disease [NCBI] 2.79742e-05
hemophilia a [NCBI] 2.52564e-05
RA [NCBI] 2.44243e-05
ALD [NCBI] 2.16408e-05
ACE [NCBI] 2.02694e-05
NF1 [NCBI] 1.87007e-05
AD [NCBI] 1.64468e-05
TTR [NCBI] 1.34054e-05
SHBG [NCBI] 1.28003e-05
PD [NCBI] 1.21748e-05
CF [NCBI] 7.99015e-06
MG [NCBI] 5.23247e-06
AVP [NCBI] 4.54159e-06
SLE [NCBI] 2.13609e-06
VEGF [NCBI] 7.46914e-07



Database Center for Life Science