|
OMIM |
Link |
Information gain |
01 |
|
nephrolithiasis, calcium oxalate
|
[NCBI]
|
0.00517881
|
|
|
APRT
|
[NCBI]
|
0.00192123
|
|
|
hypercalciuria, absorptive, 1
|
[NCBI]
|
0.000948879
|
|
|
SPP1
|
[NCBI]
|
0.000648346
|
|
|
hypouricemia, renal
|
[NCBI]
|
0.000307921
|
|
|
xanthinuria, type i
|
[NCBI]
|
0.000287256
|
|
|
UMOD
|
[NCBI]
|
0.00021885
|
|
|
dent disease 1
|
[NCBI]
|
0.000176359
|
|
|
cystinuria
|
[NCBI]
|
0.000146278
|
|
|
uric acid urolithiasis
|
[NCBI]
|
0.000136591
|
|
|
PTH
|
[NCBI]
|
9.69715e-05
|
|
|
hyperoxaluria, primary, type ii
|
[NCBI]
|
9.27854e-05
|
|
|
liddle syndrome
|
[NCBI]
|
8.0832e-05
|
|
|
renal tubular acidosis, distal, autosomal dominant
|
[NCBI]
|
7.60048e-05
|
|
|
VDR
|
[NCBI]
|
6.95829e-05
|
|
|
alkaptonuria
|
[NCBI]
|
6.61745e-05
|
|
|
bartter syndrome, type 3
|
[NCBI]
|
6.45623e-05
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
6.30979e-05
|
|
|
solute carrier family 26 (anion transporter), member 6: slc26a6
|
[NCBI]
|
5.39635e-05
|
|
|
SLC22A12
|
[NCBI]
|
5.05921e-05
|
|
|
HPRT1
|
[NCBI]
|
4.83763e-05
|
|
|
ALB
|
[NCBI]
|
4.78453e-05
|
|
|
SLC7A9
|
[NCBI]
|
3.79646e-05
|
|
|
SLC3A1
|
[NCBI]
|
3.17582e-05
|
|
|
SPARC
|
[NCBI]
|
3.02213e-05
|
|
|
CF
|
[NCBI]
|
2.80951e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
2.52668e-05
|
|
|
RA
|
[NCBI]
|
1.84051e-05
|
|
|
CDK4
|
[NCBI]
|
1.67643e-05
|
|
|
MEN1
|
[NCBI]
|
1.6133e-05
|
|
|
VEGF
|
[NCBI]
|
1.22456e-05
|
|
|
ACPP
|
[NCBI]
|
6.53981e-06
|
|
|
XDH
|
[NCBI]
|
5.85522e-06
|
|
|
EGFR
|
[NCBI]
|
4.18126e-06
|
|
|
CAT
|
[NCBI]
|
3.71117e-07
|
|
|
PCNA
|
[NCBI]
|
2.09506e-07
|
|
|
AR
|
[NCBI]
|
1.38183e-07
|
|