familial cholestasis
Classification
biliary ducts
- Alagille’s syndrome
- Norwegian cholestasis
- neonatal sclerosing cholangitis
- turkish nonsyndromic paucity of interlobular bile ducts
- north american indian cirrhosis (16q22)
lobule
- congenital anomalies of bile acid metabolism
- progressive familial intrahepatic cholestases (PFIC)
- PFIC-1 (Byler’s disease) (P-type adenosine triphosphatse - 18q21-22)
- benign recurrent intrahepatic cholestasis (BRIC) (P-type adenosine triphosphatse - 18q21-22)
- PFIC-2 (Canalicular bile acide transporte ABCB11 - 2q24)
- PFIC-3 (canalicular phospholipid transporter ABCB4 - 7q21)
Unknown origin
- Greenland Eskimo cholestasis
- indian childhood cirrhosis
- childhood cirrhosis in Arab israelis
- tyrolean infantile cirrhosis