ODCs

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

PROTEIN INTERACTIONS: 1

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

Pseudohypoaldosteronism type 2E

Congenital dyserythropoietic anemia type II


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CUL3	(0.63)	SEC23B

Citations in the biomedical literature:

Pseudohypoaldosteronism type 2E		Congenital dyserythropoietic anemia type II
	Synonym(s): - PHA2E		Synonym(s): - CDA II - CDA type 2 - CDA type II - Congenital dyserythropoietic anemia type 2 - Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas) - SEC23B-CDG

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): - Diseases of the circulatory system -		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: - 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: adult Type of inheritance: autosomal recessive

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

No signs/symptoms info available.