|
1
|
(HPO:0000979)
|
Purpura |
|
|
|
|
27 / 7739
|
|
2
|
(HPO:0001250)
|
Seizures |
|
|
|
|
1245 / 7739
|
|
3
|
(HPO:0001263)
|
Global developmental delay |
|
|
|
|
853 / 7739
|
|
4
|
(HPO:0002204)
|
Pulmonary embolism |
|
|
|
|
26 / 7739
|
|
5
|
(HPO:0002625)
|
Deep venous thrombosis |
|
|
|
|
10 / 7739
|
|
6
|
(HPO:0002638)
|
Superficial thrombophlebitis |
|
|
|
|
6 / 7739
|
|
7
|
(HPO:0005543)
|
Reduced protein C activity |
|
|
|
|
4 / 7739
|
|
8
|
(HPO:0007902)
|
Vitreous hemorrhage |
|
|
|
|
9 / 7739
|
|
9
|
(OMIM)
|
Neonatal vitreous hemorrhages |
|
|
|
|
1 / 7739
|
|
10
|
(OMIM)
|
Intraabdominal venous thrombosis |
|
|
|
|
1 / 7739
|
|
11
|
(OMIM)
|
Neonatal purpura fulminans |
|
|
|
|
2 / 7739
|
|
12
|
(OMIM)
|
Cerebral palsy, spastic |
|
|
|
|
2 / 7739
|
|
13
|
(OMIM)
|
Periventricular hemorrhagic infarction |
|
|
|
|
1 / 7739
|
|
14
|
(OMIM)
|
Plasma protein C deficiency |
|
|
|
|
2 / 7739
|
|
15
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
16
|
(HPO:0003828)
|
Variable expressivity |
|
|
|
|
130 / 7739
|
|
17
|
(HPO:0100724)
|
Hypercoagulability |
|
|
|
|
15 / 7739
|