Progressive familial intrahepatic cholestasis type 1

PFIC1, a type of progressive familial intrahepathic cholestasis (PFIC), is an infantile hereditary disorder in bile formation that is hepatocellular in origin and associated with extrahepatic features.

Also known as: Byler disease, FIC1 deficiency, PFIC1, cholestasis, progressive familial intrahepatic 1, cholestasis, progressive familial intrahepatic, type 1, Byler's disease, cholestasis, fatal intrahepatic, cholestasis, progressive familial intrahepatic, 1

11 clinical trials for this condition and its sub-types, 4 tagged with Progressive familial intrahepatic cholestasis type 1 itself.