|
1
|
(HPO:0000093)
|
Proteinuria |
|
|
|
|
169 / 7739
|
|
2
|
(HPO:0000097)
|
Focal segmental glomerulosclerosis |
|
|
|
|
37 / 7739
|
|
3
|
(HPO:0000100)
|
Nephrotic syndrome |
|
|
|
|
83 / 7739
|
|
4
|
(HPO:0000969)
|
Edema |
|
|
|
|
117 / 7739
|
|
5
|
(HPO:0003073)
|
Hypoalbuminemia |
|
|
|
|
40 / 7739
|
|
6
|
(HPO:0005576)
|
Tubulointerstitial fibrosis |
|
|
|
|
32 / 7739
|
|
7
|
(OMIM)
|
Tubulointerstitial atrophy |
|
|
|
|
1 / 7739
|
|
8
|
(OMIM)
|
Minimal change disease (lipoid nephrosis) on renal biopsy |
|
|
|
|
2 / 7739
|
|
9
|
(OMIM)
|
Effacement of podocyte foot processes |
|
|
|
|
3 / 7739
|
|
10
|
(OMIM)
|
Foot process fusion |
|
|
|
|
1 / 7739
|
|
11
|
(OMIM)
|
Swollen podocytes |
|
|
|
|
1 / 7739
|
|
12
|
(OMIM)
|
Microvillus transformation of the podocytes |
|
|
|
|
1 / 7739
|
|
13
|
(OMIM)
|
Attenuation of the glomerular basement membrane |
|
|
|
|
1 / 7739
|
|
14
|
(OMIM)
|
Rare mesangial IgM deposition |
|
|
|
|
1 / 7739
|
|
15
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
16
|
(HPO:0003828)
|
Variable expressivity |
|
|
|
|
130 / 7739
|