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1186865008: Progressive familial intrahepatic cholestasis type 3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4667864010 Progressive familial intrahepatic cholestasis type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667865011 Progressive familial intrahepatic cholestasis type 3 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
7723811000241113 PFIC3 - progressive familial intrahepatic cholestasis type 3 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7723821000241118 cholestase intrahépatique familiale progressive de type 3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive familial intrahepatic cholestasis type 3 Is a 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. true Inferred relationship Some
Progressive familial intrahepatic cholestasis type 3 Clinical course Progressive true Inferred relationship Some 1
Progressive familial intrahepatic cholestasis type 3 Finding site Intrahepatic biliary tract structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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