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Primary sclerosing cholangitis

2 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Familial hypospadias

4 OMIM references -
2 associated genes
1 sign/symptom

Primary sclerosing cholangitis

Familial hypospadias

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


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

Citations in the biomedical literature:

Primary sclerosing cholangitis		Familial hypospadias
	Synonym(s): - PSC		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare hepatic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital disease

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

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

	External references: 2 OMIM references - 1 MeSH reference: C536419		External references: 4 OMIM references - No MeSH references

Familial hypospadias
	Very frequent - Hypospadias / epispadias / bent penis
Primary sclerosing cholangitis
(no data available)