ODCs

Click node...

1 associated gene
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Multiple paragangliomas associated with polycythemia

Autosomal dominant secondary polycythemia

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


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

Citations in the biomedical literature:

Multiple paragangliomas associated with polycythemia		Autosomal dominant secondary polycythemia
	Synonym(s): - Multiple paragangliomas associated with erythrocytosis - Paraganglioma - somatostatinoma - polycythemia		Synonym(s): - Autosomal dominant secondary erythrocytosis

	Classification (Orphanet): - Rare endocrine disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.