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Familial hypospadias

4 OMIM references -
2 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

Pseudohyperaldosteronism type 2

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

Familial hypospadias

Pseudohyperaldosteronism type 2

AR	(UniProt - OMIM)		NR3C2	(UniProt - OMIM)
MAMLD1	(UniProt - OMIM)


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

Citations in the biomedical literature:

Familial hypospadias		Pseudohyperaldosteronism type 2
	Synonym(s): (no synonyms)		Synonym(s): - Early-onset hypertension with exacerbation in pregnancy - Hypertension due to gain-of-function mutations in the mineralocorticoid receptor

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital disease		Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare renal disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the circulatory system -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Familial hypospadias
	Very frequent - Hypospadias / epispadias / bent penis
Pseudohyperaldosteronism type 2
(no data available)