ODCs

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

PROTEIN INTERACTIONS: 1

2 OMIM references -
1 associated gene
No signs/symptoms info

Renal pseudohypoaldosteronism type 1

Familial isolated pituitary adenoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NR3C2	(0.63)	AIP

Citations in the biomedical literature:

Renal pseudohypoaldosteronism type 1		Familial isolated pituitary adenoma
	Synonym(s): - Autosomal dominant pseudohypoaldosteronism type 1		Synonym(s): - FIPA

	Classification (Orphanet): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare endocrine disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the genitourinary system -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.