Secondary polycythemia

General Information (adopted from Orphanet):

Synonyms, Signs: Secondary erythrocytosis
Number of Symptoms 16
OrphanetNr: 98428
OMIM Id:
ICD-10: D75.1
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant
Autosomal recessive
[Orphanet]
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Genetic polycythemia
 -Rare genetic disease
Polycythemia
 -Rare hematologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0002315) Headache Very frequent [Orphanet] 175 / 7739
2
 (HPO:0004372) Reduced consciousness/confusion Very frequent [Orphanet] 73 / 7739
3
 (HPO:0100760) Clubbing of toes Frequent [Orphanet] 24 / 7739
4
 (HPO:0005244) Gastrointestinal infarctions Very frequent [Orphanet] 14 / 7739
5
 (HPO:0001513) Obesity Very frequent [Orphanet] 172 / 7739
6
 (HPO:0100761) Visceral angiomatosis Very frequent [Orphanet] 21 / 7739
7
 (HPO:0001063) Acrocyanosis Very frequent [Orphanet] 56 / 7739
8
 (HPO:0010783) Erythema Very frequent [Orphanet] 138 / 7739
9
 (HPO:0100659) Abnormality of the cerebral vasculature Very frequent [Orphanet] 25 / 7739
10
 (HPO:0005293) Venous insufficiency Very frequent [Orphanet] 27 / 7739
11
 (HPO:0002615) Hypotension Very frequent [Orphanet] 52 / 7739
12
 (HPO:0002140) Ischemic stroke Very frequent [Orphanet] 70 / 7739
13
 (HPO:0000822) Hypertension Very frequent [Orphanet] 224 / 7739
14
 (HPO:0004420) Arterial thrombosis Very frequent [Orphanet] 20 / 7739
15
 (HPO:0004936) Venous thrombosis Very frequent [Orphanet] 41 / 7739
16
 (HPO:0001877) Abnormality of erythrocytes Very frequent [Orphanet] 18 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: