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Familial hypospadias
4 OMIM references -
2 associated genes
1 sign/symptom
PROTEIN INTERACTIONS: 1
Primary sclerosing cholangitis
2 OMIM references -
3 associated genes
No signs/symptoms info
Familial hypospadias
Primary sclerosing cholangitis

AR
(UniProt - OMIM)
 GPR35
(UniProt - OMIM)
MAMLD1
(UniProt - OMIM)
 MST1
(UniProt - OMIM)
TCF4
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
AR
(0.88)
TCF4


Citations in the biomedical literature:


Familial hypospadias
AR MAMLD1
Primary sclerosing cholangitis
GPR35 MST1 TCF4



Familial hypospadias
Primary sclerosing cholangitis

Synonym(s):
(no synonyms)

Synonym(s):
- PSC
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare urogenital disease
Classification (Orphanet):
- Rare hepatic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
4 OMIM references -
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C536419
Familial hypospadias

Very frequent
- Hypospadias / epispadias / bent penis



Primary sclerosing cholangitis

(no data available)