ODCs

Click node...

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

PROTEIN INTERACTIONS: 2

6 OMIM references -
4 associated genes
No signs/symptoms info

Pseudohypoaldosteronism type 2E

Congenital fibrosis of extraocular muscles


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CUL3 CUL3	(0.63) (0.63)	TUBB2B TUBB3

Citations in the biomedical literature:

Pseudohypoaldosteronism type 2E		Congenital fibrosis of extraocular muscles
	Synonym(s): - PHA2E		Synonym(s): - FEOM

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Diseases of the eye and adnexa -

	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: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 6 OMIM references - No MeSH references

No signs/symptoms info available.