|
1
|
(HPO:0000037)
|
Male pseudohermaphroditism |
Very frequent [Orphanet]
|
|
|
|
25 / 7739
|
|
2
|
(HPO:0000100)
|
Nephrotic syndrome |
Frequent [Orphanet]
|
|
|
|
83 / 7739
|
|
3
|
(HPO:0000083)
|
Renal insufficiency |
Frequent [Orphanet]
|
|
|
|
232 / 7739
|
|
4
|
(HPO:0000093)
|
Proteinuria |
Frequent [Orphanet]
|
|
|
|
169 / 7739
|
|
5
|
(HPO:0100820)
|
Glomerulopathy |
Frequent [Orphanet]
|
|
|
|
46 / 7739
|
|
6
|
(HPO:0000786)
|
Primary amenorrhea |
Very frequent [Orphanet]
|
|
|
|
61 / 7739
|
|
7
|
(HPO:0000097)
|
Focal segmental glomerulosclerosis |
|
|
|
|
37 / 7739
|
|
8
|
(HPO:0000133)
|
Gonadal dysgenesis |
|
|
|
|
21 / 7739
|
|
9
|
(HPO:0000149)
|
Ovarian gonadoblastoma |
|
|
|
|
2 / 7739
|
|
10
|
(HPO:0003774)
|
Stage 5 chronic kidney disease |
|
|
|
|
78 / 7739
|
|
11
|
(HPO:0000150)
|
Gonadoblastoma |
|
|
|
|
8 / 7739
|
|
12
|
(HPO:0008373)
|
Puberty and gonadal disorders |
Very frequent [Orphanet]
|
|
|
|
156 / 7739
|
|
13
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
14
|
(HPO:0001428)
|
Somatic mutation |
|
|
|
|
100 / 7739
|