|
1
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
2
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
3
|
(HPO:0000822)
|
Hypertension |
|
|
|
|
224 / 7739
|
|
4
|
(HPO:0000979)
|
Purpura |
|
|
|
|
27 / 7739
|
|
5
|
(HPO:0001250)
|
Seizures |
|
|
|
|
1245 / 7739
|
|
6
|
(HPO:0001259)
|
Coma |
|
|
|
|
65 / 7739
|
|
7
|
(HPO:0001269)
|
Hemiparesis |
|
|
|
|
51 / 7739
|
|
8
|
(HPO:0001873)
|
Thrombocytopenia |
|
|
|
|
224 / 7739
|
|
9
|
(HPO:0001919)
|
Acute kidney injury |
|
|
|
|
21 / 7739
|
|
10
|
(HPO:0001923)
|
Reticulocytosis |
|
|
|
|
28 / 7739
|
|
11
|
(HPO:0001937)
|
Microangiopathic hemolytic anemia |
|
|
|
|
12 / 7739
|
|
12
|
(HPO:0001945)
|
Fever |
|
|
|
|
218 / 7739
|
|
13
|
(HPO:0001981)
|
Schistocytosis |
|
|
|
|
7 / 7739
|
|
14
|
(HPO:0002014)
|
Diarrhea |
|
|
|
|
225 / 7739
|
|
15
|
(HPO:0002357)
|
Dysphasia |
|
|
|
|
33 / 7739
|
|
16
|
(HPO:0003077)
|
Hyperlipidemia |
|
|
|
|
37 / 7739
|
|
17
|
(HPO:0003138)
|
Increased blood urea nitrogen |
|
|
|
|
14 / 7739
|
|
18
|
(HPO:0003259)
|
Elevated serum creatinine |
|
|
|
|
31 / 7739
|
|
19
|
(HPO:0005356)
|
Decreased serum complement factor I |
|
|
|
|
3 / 7739
|
|
20
|
(HPO:0005369)
|
Decreased serum complement factor H |
|
|
|
|
4 / 7739
|
|
21
|
(HPO:0005416)
|
Decreased serum complement factor B |
|
|
|
|
6 / 7739
|
|
22
|
(HPO:0005421)
|
Decreased serum complement C3 |
|
|
|
|
9 / 7739
|
|
23
|
(HPO:0005575)
|
Hemolytic-uremic syndrome |
|
|
|
|
11 / 7739
|
|
24
|
(HPO:0100519)
|
Anuria |
|
|
|
|
20 / 7739
|
|
25
|
(HPO:0100543)
|
Cognitive impairment |
|
|
|
|
230 / 7739
|