|
OMIM |
Link |
Information gain |
01 |
|
hyperreninemic hypoaldosteronism, familial, 2
|
[NCBI]
|
0.00159179
|
|
|
corticosterone methyloxidase type ii deficiency
|
[NCBI]
|
0.000354253
|
|
|
CYP11B2
|
[NCBI]
|
0.000136143
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
0.000110801
|
|
|
liddle syndrome
|
[NCBI]
|
9.63076e-05
|
|
|
PHA2
|
[NCBI]
|
8.77542e-05
|
|
|
SCNN1A
|
[NCBI]
|
6.724e-05
|
|
|
IL6
|
[NCBI]
|
4.17052e-05
|
|
|
ALD
|
[NCBI]
|
3.82965e-05
|
|
|
FMF
|
[NCBI]
|
3.22336e-05
|
|
|
PTH
|
[NCBI]
|
9.14044e-06
|
|
|
SLE
|
[NCBI]
|
1.36693e-08
|
|