ODCs

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

COMMON GENES: 1

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

Renal pseudohypoaldosteronism type 1

Pseudohyperaldosteronism type 2

Citations in the biomedical literature:

Renal pseudohypoaldosteronism type 1		Pseudohyperaldosteronism type 2
	Synonym(s): - Autosomal dominant pseudohypoaldosteronism type 1		Synonym(s): - Early-onset hypertension with exacerbation in pregnancy - Hypertension due to gain-of-function mutations in the mineralocorticoid receptor

	Classification (Orphanet): - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare renal disease

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

	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: (no data available)

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

No signs/symptoms info available.