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Up to: Progressive familial intrahepatic cholestasis
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.
This condition has no sub-types.