Symptom Information: Sort according to HPO 

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