|
OMIM |
Link |
Information gain |
01 |
|
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
|
|