1
|
(HPO:0000100)
|
Nephrotic syndrome |
Very frequent [Orphanet]
|
|
|
|
83 / 7739
|
2
|
(HPO:0000093)
|
Proteinuria |
Very frequent [Orphanet]
|
|
|
|
169 / 7739
|
3
|
(HPO:0000083)
|
Renal insufficiency |
|
|
|
|
232 / 7739
|
4
|
(HPO:0000092)
|
Tubular atrophy |
|
|
|
|
28 / 7739
|
5
|
(HPO:0000821)
|
Hypothyroidism |
|
|
|
|
141 / 7739
|
6
|
(HPO:0000969)
|
Edema |
|
|
|
|
117 / 7739
|
7
|
(HPO:0001510)
|
Growth delay |
|
|
|
|
295 / 7739
|
8
|
(HPO:0001518)
|
Small for gestational age |
|
|
|
|
107 / 7739
|
9
|
(HPO:0001967)
|
Diffuse mesangial sclerosis |
|
|
|
|
11 / 7739
|
10
|
(HPO:0002020)
|
Gastroesophageal reflux |
|
|
|
|
101 / 7739
|
11
|
(HPO:0002021)
|
Pyloric stenosis |
|
|
|
|
51 / 7739
|
12
|
(HPO:0002643)
|
Neonatal respiratory distress |
|
|
|
|
22 / 7739
|
13
|
(HPO:0002719)
|
Recurrent infections |
|
|
|
|
107 / 7739
|
14
|
(HPO:0003073)
|
Hypoalbuminemia |
|
|
|
|
40 / 7739
|
15
|
(HPO:0003075)
|
Hypoproteinemia |
|
|
|
|
27 / 7739
|
16
|
(HPO:0003077)
|
Hyperlipidemia |
|
|
|
|
37 / 7739
|
17
|
(HPO:0003270)
|
Abdominal distention |
|
|
|
|
46 / 7739
|
18
|
(HPO:0008677)
|
Congenital nephrotic syndrome |
|
|
|
|
1 / 7739
|
19
|
(OMIM)
|
Proteinuria, severe |
|
|
|
|
1 / 7739
|
20
|
(OMIM)
|
Biopsy shows dilated proximal tubules |
|
|
|
|
1 / 7739
|
21
|
(OMIM)
|
Interstitial fibrosis |
|
|
|
|
24 / 7739
|
22
|
(OMIM)
|
Mesangial cell proliferation |
|
|
|
|
4 / 7739
|
23
|
(OMIM)
|
Glomerulosclerosis and fibrosis |
|
|
|
|
1 / 7739
|
24
|
(OMIM)
|
Loss of podocyte foot processes |
|
|
|
|
2 / 7739
|
25
|
(OMIM)
|
Increased alpha-fetoprotein |
|
|
|
|
5 / 7739
|
26
|
(HPO:0000107)
|
Renal cyst |
Very frequent [Orphanet]
|
|
|
|
126 / 7739
|
27
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
28
|
(HPO:0003577)
|
Congenital onset |
|
|
|
|
133 / 7739
|
29
|
(HPO:0003678)
|
Rapidly progressive |
|
|
|
|
33 / 7739
|