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Up to: Syndromic disease · Inborn disorder of bilirubin metabolism · Familial intrahepatic cholestasis

Progressive familial intrahepatic cholestasis

Progressive familial intrahepatic cholestasis (PFIC) refers to a heterogeneous group of autosomal recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin.

16 trials tagged with this condition →

Progressive familial intrahepatic cholestasis type 1 4 trials
Progressive familial intrahepatic cholestasis type 2 4 trials
Cholestasis, progressive familial intrahepatic, 4 2 trials
Progressive familial intrahepatic cholestasis type 3 2 trials
Cholestasis, progressive familial intrahepatic, 5 1 trial
Cholestasis, progressive familial intrahepatic, 6 1 trial
Hereditary North American Indian childhood cirrhosis 1 trial
MYO5B-related progressive familial intrahepatic cholestasis 0 trials
Benign recurrent intrahepatic cholestasis type 1 0 trials
Cholestasis, progressive familial intrahepatic, 10 0 trials
Cholestasis, progressive familial intrahepatic, 11 0 trials
Cholestasis, progressive familial intrahepatic, 12 0 trials
Cholestasis, progressive familial intrahepatic, 13 0 trials
Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss 0 trials
Cholestasis, progressive familial intrahepatic, 8 0 trials
Cholestasis, progressive familial intrahepatic, 9 0 trials