Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Urologic Diseases	[NCBI]

Gene	Link	Information Gain
VUR	[NCBI]	0.000702137
UFS	[NCBI]	0.000229071
MS	[NCBI]	7.77466e-05
UMOD	[NCBI]	6.99773e-05
AMBP	[NCBI]	3.27225e-05
HNF1B	[NCBI]	1.32537e-05
CST3	[NCBI]	1.04709e-05
UPK1B	[NCBI]	1.03847e-05
MUC7	[NCBI]	9.73364e-06
ACE	[NCBI]	9.53296e-06
UPK2	[NCBI]	9.0086e-06
LOX	[NCBI]	8.68635e-06
AGTR2	[NCBI]	8.41533e-06
PTGER1	[NCBI]	7.52465e-06
PAX2	[NCBI]	7.25067e-06
FBN1	[NCBI]	7.23667e-06
TRPV1	[NCBI]	7.19535e-06
XRCC3	[NCBI]	6.75448e-06
SOD2	[NCBI]	6.25025e-06
PDE5A	[NCBI]	5.57912e-06
CTLA4	[NCBI]	5.49273e-06
XRCC1	[NCBI]	5.40119e-06
ALK	[NCBI]	5.30113e-06
KRT20	[NCBI]	4.91686e-06
TTR	[NCBI]	4.75383e-06
SOD1	[NCBI]	3.51429e-06
BIRC5	[NCBI]	3.28924e-06
PTEN	[NCBI]	3.07002e-06
HGF	[NCBI]	2.88453e-06
VEGFA	[NCBI]	2.26036e-06
TP53	[NCBI]	2.2554e-06
PCNA	[NCBI]	2.12173e-06
EGF	[NCBI]	1.43218e-06

OMIM	Link	Information gain
UFS	[NCBI]	0.00177835
megaduodenum and/or megacystis	[NCBI]	0.00146918
EEC1	[NCBI]	0.000486801
KLK3	[NCBI]	0.000218484
cutis laxa, autosomal recessive, type i	[NCBI]	0.000195114
epithelial squamous dysplasia, keratinizing desquamative, of urinary tract	[NCBI]	0.000150059
ACPP	[NCBI]	8.61253e-05
cutis laxa, x-linked	[NCBI]	8.20324e-05
MADA	[NCBI]	8.13853e-05
OCA2	[NCBI]	7.47252e-05
CGD	[NCBI]	6.24343e-05
AGTR2	[NCBI]	5.90902e-05
danubian endemic familial nephropathy	[NCBI]	5.86343e-05
BIRC5	[NCBI]	4.94573e-05
MJD	[NCBI]	4.4055e-05
PSAP	[NCBI]	4.03164e-05
polycystic kidneys	[NCBI]	3.79657e-05
ALK	[NCBI]	2.31059e-05
ACE	[NCBI]	2.06329e-05
GNRH1	[NCBI]	1.86663e-05
TTR	[NCBI]	1.3748e-05
RNASE3	[NCBI]	1.03663e-05
HGF	[NCBI]	5.76878e-06
PCNA	[NCBI]	2.26502e-06
RA	[NCBI]	1.2981e-06
VEGF	[NCBI]	5.89348e-07
EGF	[NCBI]	3.36792e-07