Biliary atresia

rare

A rare, biliary tract disease characterized by progressive obliterative cholangiopathy of the intra- and extrahepatic bile ducts, occurring in the embryonic/ perinatal period, leading to severe and persistent neonatal jaundice and acholic stool.

Identifiers: MONDO:0008867 Orphanet:30391
Part of: Cholestasis Non-neoplastic bile duct disorder
Also known as: atresia of bile ducts · biliary atresia, congenital · congenital biliary atresia · isolated atresia of bile ducts · non-syndromic biliary atresia

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Biliary atresia intrahepatic non syndromic form	MONDO:0022573
Biliary atresia intrahepatic syndromic form	MONDO:0022574
Extrahepatic biliary atresia	MONDO:0100285

Projects

Including projects on subtypes.

No projects yet.