Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Kidney Concentrating Ability	[NCBI]

Gene	Link	Information Gain
AVP	[NCBI]	9.31e-05
AQP2	[NCBI]	6.40071e-05
SLC12A1	[NCBI]	1.77245e-05
SLC9A3	[NCBI]	1.40637e-05
UMOD	[NCBI]	1.40289e-05
CLCNKA	[NCBI]	9.33195e-06
PTH	[NCBI]	7.9372e-06
PKD1	[NCBI]	3.59697e-06
SLC14A2	[NCBI]	3.20043e-06
SLC14A1	[NCBI]	2.85633e-06
BSND	[NCBI]	2.77188e-06
NFAT5	[NCBI]	2.48462e-06
OCRL	[NCBI]	2.44543e-06
PKHD1	[NCBI]	2.43799e-06
KCNJ1	[NCBI]	2.26761e-06
SOX2	[NCBI]	1.99994e-06
KLF4	[NCBI]	1.94211e-06
PTGER1	[NCBI]	1.86938e-06
FGF23	[NCBI]	1.82543e-06
MIP	[NCBI]	1.82164e-06
GHR	[NCBI]	1.66681e-06
SGK1	[NCBI]	1.62478e-06
CST3	[NCBI]	1.23289e-06

OMIM	Link	Information gain
AVP	[NCBI]	0.00146887
diabetes insipidus, nephrogenic, autosomal	[NCBI]	0.000342209
diabetes insipidus, nephrogenic, x-linked	[NCBI]	0.000301721
renal tubular acidosis, distal, autosomal dominant	[NCBI]	0.000224108
BBS	[NCBI]	0.000208995
hyperlysinuria with hyperammonemia	[NCBI]	0.000161702
diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification	[NCBI]	0.000161702
renal tubular acidosis, proximal	[NCBI]	0.000161702
AQP2	[NCBI]	0.000159242
sickle cell anemia	[NCBI]	0.000157181
polycystic kidneys	[NCBI]	0.000148796
AI1G	[NCBI]	0.000123457
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation	[NCBI]	0.0001116
CO	[NCBI]	0.000104223
JK	[NCBI]	9.14195e-05
dent disease 1	[NCBI]	8.81815e-05
NPHP1	[NCBI]	8.33235e-05
bartter syndrome, type 3	[NCBI]	7.94256e-05
WFS1	[NCBI]	7.03681e-05
SLC12A3	[NCBI]	5.18312e-05
AQP3	[NCBI]	4.9284e-05
AVPR2	[NCBI]	4.71915e-05
AQP1	[NCBI]	3.72639e-05
RA	[NCBI]	2.59739e-05
NPPA	[NCBI]	2.30216e-05
PTH	[NCBI]	1.90338e-05
von willebrand disease	[NCBI]	1.22368e-05
hemophilia a	[NCBI]	1.0596e-05
GHR	[NCBI]	8.07543e-06