ODCs

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

PROTEIN INTERACTIONS: 1

6 associated genes
No signs/symptoms info

Pseudohyperaldosteronism type 2

Childhood-onset nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NR3C2	(0.52)	ACTA1

Citations in the biomedical literature:

Pseudohyperaldosteronism type 2		Childhood-onset nemaline myopathy
	Synonym(s): - Early-onset hypertension with exacerbation in pregnancy - Hypertension due to gain-of-function mutations in the mineralocorticoid receptor		Synonym(s): - Mild nemaline myopathy

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.