Progressive familial intrahepatic cholestasis type 3 (Q65607): Difference between revisions
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13 August 2026
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Latest 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. |
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CID11:ID_1276600959
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dki-india-ID_1276600959
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Concluído
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13 August 2026
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