Progressive familial intrahepatic cholestasis type 1

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Name:
Progressive familial intrahepatic cholestasis type 1
Description:
PFIC1, a type of progressive familial intrahepathic cholestasis (PFIC, see this term), is an infantile hereditary disorder in bile formation that is hepatocellular in origin and associated with extrahepatic features.
ORPHAcode:
79306
Synonyms:
Byler disease
FIC1 deficiency
PFIC1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14