|
1
|
(HPO:0000093)
|
Proteinuria |
|
|
|
|
169 / 7739
|
|
2
|
(HPO:0000790)
|
Hematuria |
|
|
|
|
106 / 7739
|
|
3
|
(HPO:0000822)
|
Hypertension |
variable [HPO:skoehler]
|
|
|
|
224 / 7739
|
|
4
|
(HPO:0001873)
|
Thrombocytopenia |
|
|
|
|
224 / 7739
|
|
5
|
(HPO:0001919)
|
Acute kidney injury |
|
|
|
|
21 / 7739
|
|
6
|
(HPO:0001937)
|
Microangiopathic hemolytic anemia |
|
|
|
|
12 / 7739
|
|
7
|
(HPO:0003138)
|
Increased blood urea nitrogen |
|
|
|
|
14 / 7739
|
|
8
|
(HPO:0003259)
|
Elevated serum creatinine |
|
|
|
|
31 / 7739
|
|
9
|
(HPO:0100519)
|
Anuria |
|
|
|
|
20 / 7739
|
|
10
|
(MedDRA:10043645)
|
Thrombotic microangiopathy |
|
|
|
|
11 / 7739
|
|
11
|
(OMIM)
|
Fragmented erythrocytes |
|
|
|
|
5 / 7739
|
|
12
|
(HPO:0001903)
|
Anemia |
|
|
|
|
289 / 7739
|
|
13
|
(OMIM)
|
Defective complement regulation |
|
|
|
|
8 / 7739
|
|
14
|
(OMIM)
|
Decreased or normal serum C3 |
|
|
|
|
5 / 7739
|
|
15
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
16
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
17
|
(HPO:0005575)
|
Hemolytic-uremic syndrome |
|
|
|
|
11 / 7739
|