5C58.03 Progressive familial intrahepatic cholestasis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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. Three types of PFIC have been identified and are related to mutations in hepatocellular transport system genes involved in bile formation. PFIC1 and PFIC2 usually appear in the first months of life, whereas onset of PFIC3 may also occur later in infancy, in childhood or even during young adulthood.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Progressive familial intrahepatic cholestasis
- PFIC - [Progressive familial intrahepatic cholestasis]
- Progressive familial intrahepatic cholestasis type 1
- PFIC1 - [Progressive familial intrahepatic cholestasis type 1]
- Progressive familial intrahepatic cholestasis type 2
- PFIC2 - [Progressive familial intrahepatic cholestasis type 2]
- Progressive familial intrahepatic cholestasis type 3
- PFIC3 - [Progressive familial intrahepatic cholestasis type 3]
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