Progressive familial intrahepatic cholestasis type 3 (Q65607): Difference between revisions
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Colestase intra-hepática familiar progressiva tipo 3 (PFIC3), um tipo de colestase intra-hepática familiar progressiva (PIFC), é transtorno hereditário da formação da bile de inicio tardio, de origem hepatocelular, caracterizada por colestase e com evolução para cirrose biliar secundária. | |||
| description / en | description / en | ||
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 characterised by cholestasis and evolving into secondary biliary cirrhosis. | |||
Revision as of 13:20, 14 August 2026
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 characterised by cholestasis and evolving into secondary biliary cirrhosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1276600959 |
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| English | 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 characterised by cholestasis and evolving into secondary biliary cirrhosis. |
