Symptom Information: Sort according to HPO 

1
(HPO:0000093) Proteinuria 169 / 7739
2
(HPO:0000100) Nephrotic syndrome 83 / 7739
3
(HPO:0001873) Thrombocytopenia rare [HPO:skoehler] 224 / 7739
4
(HPO:0001878) Hemolytic anemia rare [HPO:skoehler] 83 / 7739
5
(HPO:0001919) Acute kidney injury 21 / 7739
6
(HPO:0003774) Stage 5 chronic kidney disease rare [HPO:skoehler] 78 / 7739
7
(HPO:0004722) Thickening of the glomerular basement membrane 12 / 7739
8
(HPO:0005575) Hemolytic-uremic syndrome rare [HPO:skoehler] 11 / 7739
9
(OMIM) Membranoproliferative glomerulonephritis seen on biopsy 2 / 7739
10
(OMIM) Splitting of the basement membrane 2 / 7739
11
(OMIM) Focal capillary obliteration 2 / 7739
12
(OMIM) Mesangial cell proliferation 4 / 7739
13
(OMIM) Effacement of podocyte foot processes 3 / 7739
14
(OMIM) Patchy deposition of IgG and IgM 2 / 7739
15
(OMIM) Subendothelial deposits 2 / 7739
16
(OMIM) Swelling of endothelial cells 2 / 7739
17
(OMIM) Chronic thrombotic microangiopathy 2 / 7739
18
(OMIM) Low serum albumin 3 / 7739
19
(OMIM) Normal serum complement levels 2 / 7739
20
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
21
(HPO:0003676) Progressive disorder 148 / 7739