ODCs

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

PROTEIN INTERACTIONS: 1

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

Pseudohypoaldosteronism type 2E

Syndromic diarrhea

CUL3	(UniProt - OMIM)		SKIV2L	(UniProt - OMIM)
			TTC37	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CUL3	(0.63)	TTC37

Citations in the biomedical literature:

Pseudohypoaldosteronism type 2E		Syndromic diarrhea
	Synonym(s): - PHA2E		Synonym(s): - Phenotypic diarrhea - SD/THE - Syndromatic diarrhea - Syndromic diarrhea/Tricho-hepato-enteric syndrome - Tricho-hepato-enteric syndrome

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic disease - Rare hepatic disease

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): (no data available)

	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: neonatal/infancy Average age of death: child / adolescent Type of inheritance: autosomal recessive

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

No signs/symptoms info available.