Cytoscape Web
Click node...

Pseudohyperaldosteronism type 2
1 OMIM reference -
1 associated gene
18 connected diseases
No signs/symptoms info
Disease Type of connection
Renal pseudohypoaldosteronism type 1
Papillary or follicular thyroid carcinoma
Glucocorticoid resistance
Acromegaly
Cerebellar ataxia - hypogonadism
Complete androgen insensitivity syndrome
Familial hypospadias
Familial isolated pituitary adenoma
Kennedy disease
Partial androgen insensitivity syndrome
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Baraitser-Winter syndrome
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
Synonym(s):
- Early-onset hypertension with exacerbation in pregnancy
- Hypertension due to gain-of-function mutations in the mineralocorticoid receptor
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare renal disease
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
NR3C2 P08235600983
No signs/symptoms info available.