1
|
(HPO:0001324)
|
Muscle weakness |
Frequent [Orphanet]
|
|
|
|
859 / 7739
|
2
|
(HPO:0000112)
|
Nephropathy |
Frequent [Orphanet]
|
|
|
|
92 / 7739
|
3
|
(HPO:0002900)
|
Hypokalemia |
Very frequent [Orphanet]
|
|
|
|
45 / 7739
|
4
|
(HPO:0000083)
|
Renal insufficiency |
Frequent [Orphanet]
|
|
|
|
232 / 7739
|
5
|
(HPO:0002140)
|
Ischemic stroke |
Frequent [Orphanet]
|
|
|
|
70 / 7739
|
6
|
(HPO:0011675)
|
Arrhythmia |
Very frequent [Orphanet]
|
|
|
|
226 / 7739
|
7
|
(HPO:0002019)
|
Constipation |
Very frequent [Orphanet]
|
|
|
|
194 / 7739
|
8
|
(HPO:0000822)
|
Hypertension |
Very frequent [Orphanet]
|
|
|
|
224 / 7739
|
9
|
(HPO:0001949)
|
Hypokalemic alkalosis |
|
|
|
|
5 / 7739
|
10
|
(HPO:0003351)
|
Decreased circulating renin level |
|
|
|
|
8 / 7739
|
11
|
(HPO:0004319)
|
Hypoaldosteronism |
|
|
|
|
9 / 7739
|
12
|
(MedDRA:10037113)
|
Pseudoaldosteronism |
|
|
|
|
1 / 7739
|
13
|
(OMIM)
|
Renal epithelial sodium channel defect |
|
|
|
|
1 / 7739
|
14
|
(MedDRA:10038557)
|
Renin decreased |
|
|
|
|
2 / 7739
|
15
|
(OMIM)
|
Decreased angiotensin |
|
|
|
|
1 / 7739
|
16
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|