|
1
|
(HPO:0000618)
|
Blindness |
|
|
|
|
124 / 7739
|
|
2
|
(HPO:0002204)
|
Pulmonary embolism |
|
|
|
|
26 / 7739
|
|
3
|
(HPO:0002638)
|
Superficial thrombophlebitis |
|
|
|
|
6 / 7739
|
|
4
|
(HPO:0004420)
|
Arterial thrombosis |
|
|
|
|
20 / 7739
|
|
5
|
(HPO:0005305)
|
Cerebral venous thrombosis |
|
|
|
|
7 / 7739
|
|
6
|
(HPO:0005521)
|
Disseminated intravascular coagulation |
|
|
|
|
5 / 7739
|
|
7
|
(OMIM)
|
Retinal thrombosis |
|
|
|
|
1 / 7739
|
|
8
|
(OMIM)
|
Impaired retinal vasculogenesis |
|
|
|
|
1 / 7739
|
|
9
|
(HPO:0004850)
|
Recurrent deep vein thrombosis |
|
|
|
|
4 / 7739
|
|
10
|
(OMIM)
|
Mesenteric thrombosis |
|
|
|
|
2 / 7739
|
|
11
|
(HPO:0001342)
|
Cerebral hemorrhage |
|
|
|
|
24 / 7739
|
|
12
|
(OMIM)
|
Neonatal purpura fulminans |
|
|
|
|
2 / 7739
|
|
13
|
(MedDRA:10040893)
|
Skin necrosis |
|
|
|
|
1 / 7739
|
|
14
|
(OMIM)
|
Absent/reduced free proteins and absent total protein S |
|
|
|
|
1 / 7739
|
|
15
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
16
|
(HPO:0100724)
|
Hypercoagulability |
|
|
|
|
15 / 7739
|