Symptom Information: Sort according to HPO 

1
(HPO:0000037) Male pseudohermaphroditism Very frequent [Orphanet] 25 / 7739
2
(HPO:0000112) Nephropathy Very frequent [Orphanet] 92 / 7739
3
(HPO:0002667) Nephroblastoma Very frequent [Orphanet] 30 / 7739
4
(HPO:0000100) Nephrotic syndrome Very frequent [Orphanet] 83 / 7739
5
(HPO:0000093) Proteinuria Very frequent [Orphanet] 169 / 7739
6
(HPO:0000822) Hypertension Frequent [Orphanet] 224 / 7739
7
(HPO:0000133) Gonadal dysgenesis Occasional [Orphanet] 21 / 7739
8
(HPO:0000033) Ambiguous genitalia, male 9 / 7739
9
(HPO:0000061) Ambiguous genitalia, female 8 / 7739
10
(HPO:0000097) Focal segmental glomerulosclerosis 37 / 7739
11
(HPO:0000149) Ovarian gonadoblastoma 2 / 7739
12
(HPO:0000776) Congenital diaphragmatic hernia 36 / 7739
13
(HPO:0001967) Diffuse mesangial sclerosis 11 / 7739
14
(HPO:0003248) Gonadal tissue inappropriate for external genitalia or chromosomal sex 1 / 7739
15
(HPO:0003774) Stage 5 chronic kidney disease 78 / 7739
16
(HPO:0010459) True hermaphroditism 5 / 7739
17
(HPO:0000062) Ambiguous genitalia 74 / 7739
18
(HPO:0000150) Gonadoblastoma 8 / 7739
19
(OMIM) Chronic/endstage renal failure 1 / 7739
20
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
21
(HPO:0001428) Somatic mutation 100 / 7739