Biliary atresia

MONDO:0008867

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.

Also known as: atresia of bile ducts, biliary atresia, congenital, congenital biliary atresia, isolated atresia of bile ducts, non-syndromic biliary atresia, isolated biliary atresia

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