ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Autosomal dominant secondary polycythemia

Acute myeloid leukemia with t(8;16)(p11;p13) translocation

EGLN1	(UniProt - OMIM)		CREBBP	(UniProt - OMIM)
EPAS1	(UniProt - OMIM)		KAT6A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EPAS1	(0.63)	CREBBP

Citations in the biomedical literature:

Autosomal dominant secondary polycythemia		Acute myeloid leukemia with t(8;16)(p11;p13) translocation
	Synonym(s): - Autosomal dominant secondary erythrocytosis		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.