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Autosomal dominant secondary polycythemia
2 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Multiple paragangliomas associated with polycythemia
1 associated gene
No signs/symptoms info
Autosomal dominant secondary polycythemia
Multiple paragangliomas associated with polycythemia

EGLN1
(UniProt - OMIM)
 EPAS1
(UniProt - OMIM)
EPAS1
(UniProt - OMIM)

COMMON
GENES 		EPAS1
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EGLN1
(0.89)
EPAS1


Citations in the biomedical literature:


Autosomal dominant secondary polycythemia
EGLN1 EPAS1
Multiple paragangliomas associated with polycythemia



Autosomal dominant secondary polycythemia
Multiple paragangliomas associated with polycythemia

Synonym(s):
- Autosomal dominant secondary erythrocytosis
Synonym(s):
- Multiple paragangliomas associated with erythrocytosis
- Paraganglioma - somatostatinoma - polycythemia
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.