Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Progressive familial intrahepatic cholestasis · Benign recurrent intrahepatic cholestasis type 2
Progressive familial intrahepatic cholestasis type 2
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome.
This condition has no sub-types.