Symptom Information: Sort according to HPO 

1
(HPO:0000093) Proteinuria 169 / 7739
2
(HPO:0001289) Confusion 36 / 7739
3
(HPO:0001337) Tremor 200 / 7739
4
(HPO:0001873) Thrombocytopenia 224 / 7739
5
(HPO:0001923) Reticulocytosis 28 / 7739
6
(HPO:0001937) Microangiopathic hemolytic anemia 12 / 7739
7
(HPO:0001945) Fever 218 / 7739
8
(HPO:0001981) Schistocytosis 7 / 7739
9
(HPO:0002098) Respiratory distress Rare [HPO:skoehler] 75 / 7739
10
(HPO:0002151) Increased serum lactate 92 / 7739
11
(HPO:0002907) Microscopic hematuria 27 / 7739
12
(HPO:0003138) Increased blood urea nitrogen 14 / 7739
13
(HPO:0003259) Elevated serum creatinine 31 / 7739
14
(HPO:0005575) Hemolytic-uremic syndrome 11 / 7739
15
(HPO:0006579) Prolonged neonatal jaundice 25 / 7739
16
(MedDRA:10001052) Acute respiratory distress syndrome 3 / 7739
17
(HPO:0012211) Abnormal renal physiology 23 / 7739
18
(OMIM) Fluctuating neurologic signs 2 / 7739
19
(OMIM) Focal neurologic signs 2 / 7739
20
(HPO:0004372) Reduced consciousness/confusion 73 / 7739
21
(MedDRA:10043645) Thrombotic microangiopathy 11 / 7739
22
(HPO:0001903) Anemia 289 / 7739
23
(OMIM) Increased serum lactate dehydrogenase (LDH) 3 / 7739
24
(OMIM) Decreased serum haptoglobin 3 / 7739
25
(OMIM) Ultra large von Willebrand factor (UL-vWF) in plasma 2 / 7739
26
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
27
(HPO:0001425) Heterogeneous 132 / 7739