1
|
(HPO:0011902)
|
Abnormal hemoglobin |
Very frequent [Orphanet]
|
|
|
|
18 / 7739
|
2
|
(HPO:0000421)
|
Epistaxis |
Very frequent [Orphanet]
|
|
|
|
85 / 7739
|
3
|
(HPO:0002027)
|
Abdominal pain |
Frequent [Orphanet]
|
|
|
|
184 / 7739
|
4
|
(HPO:0000989)
|
Pruritus |
Frequent [Orphanet]
|
|
|
|
111 / 7739
|
5
|
(HPO:0002141)
|
Gait imbalance |
Very frequent [Orphanet]
|
|
|
|
55 / 7739
|
6
|
(HPO:0002321)
|
Vertigo |
|
|
|
|
58 / 7739
|
7
|
(HPO:0002093)
|
Respiratory insufficiency |
Very frequent [Orphanet]
|
|
|
|
410 / 7739
|
8
|
(HPO:0003010)
|
Prolonged bleeding time |
Occasional [Orphanet]
|
|
|
|
88 / 7739
|
9
|
(HPO:0002104)
|
Apnea |
Occasional [Orphanet]
|
|
|
|
106 / 7739
|
10
|
(HPO:0002315)
|
Headache |
Very frequent [Orphanet]
|
|
|
|
175 / 7739
|
11
|
(HPO:0005059)
|
Arthralgia/arthritis |
Frequent [Orphanet]
|
|
|
|
141 / 7739
|
12
|
(HPO:0004936)
|
Venous thrombosis |
Very frequent [Orphanet]
|
|
|
|
41 / 7739
|
13
|
(HPO:0002140)
|
Ischemic stroke |
Occasional [Orphanet]
|
|
|
|
70 / 7739
|
14
|
(HPO:0001877)
|
Abnormality of erythrocytes |
Very frequent [Orphanet]
|
|
|
|
18 / 7739
|
15
|
(HPO:0000822)
|
Hypertension |
|
|
|
|
224 / 7739
|
16
|
(HPO:0001050)
|
Plethora |
|
|
|
|
3 / 7739
|
17
|
(HPO:0001342)
|
Cerebral hemorrhage |
|
|
|
|
24 / 7739
|
18
|
(HPO:0001658)
|
Myocardial infarction |
|
|
|
|
30 / 7739
|
19
|
(HPO:0001744)
|
Splenomegaly |
|
|
|
|
337 / 7739
|
20
|
(HPO:0001898)
|
Increased red blood cell mass |
|
|
|
|
5 / 7739
|
21
|
(HPO:0001899)
|
Increased hematocrit |
|
|
|
|
6 / 7739
|
22
|
(HPO:0001900)
|
Increased hemoglobin |
|
|
|
|
7 / 7739
|
23
|
(HPO:0002641)
|
Peripheral thrombosis |
|
|
|
|
2 / 7739
|
24
|
(HPO:0002875)
|
Exertional dyspnea |
|
|
|
|
29 / 7739
|
25
|
(HPO:0012378)
|
Fatigue |
|
|
|
|
50 / 7739
|
26
|
(HPO:0001677)
|
Coronary artery disease |
|
|
|
|
58 / 7739
|
27
|
(HPO:0001901)
|
Polycythemia |
|
|
|
|
16 / 7739
|
28
|
(OMIM)
|
Normal oxygen affinity of hemoglobin |
|
|
|
|
2 / 7739
|
29
|
(OMIM)
|
Hypersensitivity of erythroid colony-forming units to erythropoietin (EPO, 133170) |
|
|
|
|
1 / 7739
|
30
|
(OMIM)
|
Low or normal serum erythropoietin |
|
|
|
|
1 / 7739
|
31
|
([DEL]MedDRA:10011224)
|
Cough |
Occasional [Orphanet]
|
|
|
|
70 / 7739
|
32
|
(HPO:0001324)
|
Muscle weakness |
Very frequent [Orphanet]
|
|
|
|
859 / 7739
|
33
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|