|
OMIM |
Link |
Information
gain |
01 |
|
|
iminoglycinuria
|
[NCBI]
|
0.0040438
|
|
|
|
histidinuria due to a renal tubular defect
|
[NCBI]
|
0.000844965
|
|
|
|
OCRL
|
[NCBI]
|
0.000709347
|
|
|
|
hypouricemia, renal
|
[NCBI]
|
0.000505045
|
|
|
|
PHA1
|
[NCBI]
|
0.000351173
|
|
|
|
PHA2
|
[NCBI]
|
0.000339312
|
|
|
|
bartter syndrome, infantile, with sensorineural deafness
|
[NCBI]
|
0.000172657
|
|
|
|
liddle syndrome
|
[NCBI]
|
0.000162313
|
|
|
|
bartter syndrome, antenatal, type 2
|
[NCBI]
|
0.000152266
|
|
|
|
hartnup disorder
|
[NCBI]
|
0.000144621
|
|
|
|
dent disease 2
|
[NCBI]
|
0.000124742
|
|
|
|
biliary malformation with renal tubular insufficiency
|
[NCBI]
|
0.000102276
|
|
|
|
HOMG4
|
[NCBI]
|
9.38016e-05
|
|
|
|
hypouricemia, familial renal, due to tubular hypersecretion
|
[NCBI]
|
9.38016e-05
|
|
|
|
hypomagnesemia, renal, with ocular involvement
|
[NCBI]
|
9.38016e-05
|
|
|
|
glycinuria with or without oxalate urolithiasis
|
[NCBI]
|
8.83005e-05
|
|
|
|
hydroxyprolinemia
|
[NCBI]
|
8.42118e-05
|
|
|
|
bartter syndrome, antenatal, type 1
|
[NCBI]
|
8.0955e-05
|
|
|
|
fumarase deficiency
|
[NCBI]
|
8.0955e-05
|
|
|
|
SLC12A1
|
[NCBI]
|
7.45227e-05
|
|
|
|
SLC22A12
|
[NCBI]
|
7.45227e-05
|
|
|
|
gitelman syndrome
|
[NCBI]
|
7.0493e-05
|
|
|
|
proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
|
[NCBI]
|
6.90246e-05
|
|
|
|
CLDN16
|
[NCBI]
|
6.6922e-05
|
|
|
|
HOMG3
|
[NCBI]
|
6.64385e-05
|
|
|
|
dent disease 1
|
[NCBI]
|
6.42127e-05
|
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
6.32061e-05
|
|
|
|
OCRL
|
[NCBI]
|
6.26709e-05
|
|
|
|
CLCN5
|
[NCBI]
|
5.74238e-05
|
|
|
|
HFTC
|
[NCBI]
|
5.33472e-05
|
|
|
|
bartter syndrome, type 3
|
[NCBI]
|
5.28315e-05
|
|
|
|
tyrosinemia, type i
|
[NCBI]
|
4.52535e-05
|
|
|
|
SLE
|
[NCBI]
|
4.1215e-05
|
|
|
|
NPPA
|
[NCBI]
|
2.00967e-05
|
|
|
|
PTH
|
[NCBI]
|
7.00447e-06
|
|
|
|
EGF
|
[NCBI]
|
6.21438e-06
|
|
