ODCs

Click node...

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

Glomuvenous malformation


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

Citations in the biomedical literature:

Pseudohypoaldosteronism type 2E		Glomuvenous malformation
	Synonym(s): - PHA2E		Synonym(s): - Glomangiomatosis - Hereditary multiple glomangiomas - Multiple glomus tumors - VMGLOM - Venous malformations with glomus cells

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare circulatory system disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536827

No signs/symptoms info available.