|
1
|
(HPO:0000963)
|
Thin skin |
Frequent [Orphanet]
|
|
|
|
96 / 7739
|
|
2
|
(HPO:0001000)
|
Abnormality of skin pigmentation |
Occasional [Orphanet]
|
|
|
|
105 / 7739
|
|
3
|
(HPO:0001933)
|
Subcutaneous hemorrhage |
Frequent [Orphanet]
|
|
|
|
50 / 7739
|
|
4
|
(HPO:0002204)
|
Pulmonary embolism |
Occasional [Orphanet]
|
|
|
|
26 / 7739
|
|
5
|
(HPO:0002625)
|
Deep venous thrombosis |
|
|
|
|
10 / 7739
|
|
6
|
(HPO:0004936)
|
Venous thrombosis |
Frequent [Orphanet]
|
|
|
|
41 / 7739
|
|
7
|
(HPO:0005293)
|
Venous insufficiency |
Occasional [Orphanet]
|
|
|
|
27 / 7739
|
|
8
|
(HPO:0100659)
|
Abnormality of the cerebral vasculature |
Occasional [Orphanet]
|
|
|
|
25 / 7739
|
|
9
|
(HPO:0100758)
|
Gangrene |
Occasional [Orphanet]
|
|
|
|
25 / 7739
|
|
10
|
(HPO:0200042)
|
Skin ulcer |
Occasional [Orphanet]
|
|
|
|
138 / 7739
|
|
11
|
(HPO:0008065)
|
Aplasia/Hypoplasia of the skin |
Frequent [Orphanet]
|
|
|
|
81 / 7739
|
|
12
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
13
|
(HPO:0000478)
|
Abnormality of the eye |
|
|
|
|
126 / 7739
|
|
14
|
(HPO:0000707)
|
Abnormality of the nervous system |
|
|
|
|
61 / 7739
|
|
15
|
(HPO:0001038)
|
Warfarin-induced skin necrosis |
|
|
|
|
3 / 7739
|
|
16
|
(HPO:0002638)
|
Superficial thrombophlebitis |
|
|
|
|
6 / 7739
|
|
17
|
(HPO:0005305)
|
Cerebral venous thrombosis |
|
|
|
|
7 / 7739
|
|
18
|
(HPO:0005543)
|
Reduced protein C activity |
|
|
|
|
4 / 7739
|
|
19
|
(HPO:0100724)
|
Hypercoagulability |
|
|
|
|
15 / 7739
|