|
1
|
(HPO:0001677)
|
Coronary artery disease |
Very frequent [Orphanet]
|
|
|
|
58 / 7739
|
|
2
|
(HPO:0001744)
|
Splenomegaly |
Frequent [Orphanet]
|
|
|
|
337 / 7739
|
|
3
|
(HPO:0001872)
|
Abnormality of thrombocytes |
Very frequent [Orphanet]
|
|
|
|
20 / 7739
|
|
4
|
(HPO:0002488)
|
Acute leukemia |
Occasional [Orphanet]
|
|
|
|
29 / 7739
|
|
5
|
(HPO:0002863)
|
Myelodysplasia |
Occasional [Orphanet]
|
|
|
|
30 / 7739
|
|
6
|
(HPO:0004936)
|
Venous thrombosis |
Very frequent [Orphanet]
|
|
|
|
41 / 7739
|
|
7
|
(HPO:0004420)
|
Arterial thrombosis |
Very frequent [Orphanet]
|
|
|
|
20 / 7739
|
|
8
|
(HPO:0005561)
|
Abnormality of bone marrow cell morphology |
Very frequent [Orphanet]
|
|
|
|
11 / 7739
|
|
9
|
(HPO:0100576)
|
Amaurosis fugax |
Very frequent [Orphanet]
|
|
|
|
13 / 7739
|
|
10
|
(HPO:0100749)
|
Chest pain |
Very frequent [Orphanet]
|
|
|
|
92 / 7739
|
|
11
|
(HPO:0011875)
|
Abnormal platelet morphology |
Very frequent [Orphanet]
|
|
|
|
8 / 7739
|
|
12
|
(HPO:0003010)
|
Prolonged bleeding time |
Very frequent [Orphanet]
|
|
|
|
88 / 7739
|
|
13
|
(HPO:0002140)
|
Ischemic stroke |
Very frequent [Orphanet]
|
|
|
|
70 / 7739
|
|
14
|
(HPO:0100659)
|
Abnormality of the cerebral vasculature |
Very frequent [Orphanet]
|
|
|
|
25 / 7739
|
|
15
|
(HPO:0001909)
|
Leukemia |
Occasional [Orphanet]
|
|
|
|
46 / 7739
|
|
16
|
(HPO:0000763)
|
Sensory neuropathy |
Very frequent [Orphanet]
|
|
|
|
78 / 7739
|
|
17
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
18
|
(HPO:0000822)
|
Hypertension |
|
|
|
|
224 / 7739
|
|
19
|
(HPO:0000924)
|
Abnormality of the skeletal system |
|
|
|
|
114 / 7739
|
|
20
|
(HPO:0001063)
|
Acrocyanosis |
|
|
|
|
56 / 7739
|
|
21
|
(HPO:0001428)
|
Somatic mutation |
|
|
|
|
100 / 7739
|
|
22
|
(HPO:0001894)
|
Thrombocytosis |
|
|
|
|
16 / 7739
|
|
23
|
(HPO:0003540)
|
Impaired platelet aggregation |
|
|
|
|
17 / 7739
|
|
24
|
(HPO:0005547)
|
Myeloproliferative disorder |
|
|
|
|
7 / 7739
|