Progressive familial intrahepatic cholestasis type 3

Progressive familial intrahepatic cholestasis type 3 (PFIC3), a type of progressive familial intrahepatic cholestasis (PFIC), is a late-onset hereditary disorder in bile formation that is hepatocellular in origin. Onset may occur from infancy to young adulthood.

Also known as: ABCB4 progressive familial intrahepatic cholestasis, MDR3 Deficiency, PFIC3, cholestasis, progressive familial intrahepatic 3, cholestasis, progressive familial intrahepatic, type 3, progressive familial intrahepatic cholestasis caused by mutation in ABCB4, Mdr3 deficiency, cholestasis, progressive familial intrahepatic, 3

10 clinical trials for this condition and its sub-types, 2 tagged with Progressive familial intrahepatic cholestasis type 3 itself.