ODCs

Click node...

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

PROTEIN INTERACTIONS: 2

1 OMIM reference -
1 associated gene
No signs/symptoms info

Autosomal dominant secondary polycythemia

Chuvash erythrocytosis

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


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EPAS1 EGLN1	(0.96) (0.82)	VHL VHL

Citations in the biomedical literature:

Autosomal dominant secondary polycythemia		Chuvash erythrocytosis
	Synonym(s): - Autosomal dominant secondary erythrocytosis		Synonym(s): - Chuvash polycythemia - Von Hippel-Lindau-dependent polycythemia

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.