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4637005: Intrahepatic cholestasis (finding)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
8746017 Intrahepatic cholestasis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
783712018 Intrahepatic cholestasis (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
50005721000188110 cholestase intrahépatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

14 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Intrahepatic cholestasis Is a Cholestasis true Inferred relationship Some
Intrahepatic cholestasis Finding site Biliary tract structure false Inferred relationship Some 1
Intrahepatic cholestasis Finding site Liver structure false Inferred relationship Some 2
Intrahepatic cholestasis Is a Finding of biliary tract true Inferred relationship Some
Intrahepatic cholestasis Finding site Intrahepatic biliary tract structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
A mild subtype of citrin deficiency characterized clinically by low birth weight, failure to thrive, transient intrahepatic cholestasis, multiple aminoacidemia, galactosemia, hypoproteinemia, hepatomegaly, decreased coagulation factors, hemolytic anemia, variable but mostly mild liver dysfunction, and hypoglycemia. Is a True Intrahepatic cholestasis Inferred relationship Some
Severe autosomal recessive intrahepatic cholestasis described in aboriginal children from northwestern Quebec. First manifestation as neonatal jaundice, progresses to periportal fibrosis and cirrhosis. Is a False Intrahepatic cholestasis Inferred relationship Some
Drug-induced intrahepatic cholestasis Is a True Intrahepatic cholestasis Inferred relationship Some
Benign recurrent intrahepatic cholestasis Is a True Intrahepatic cholestasis Inferred relationship Some
Cholestasis of pregnancy Is a True Intrahepatic cholestasis Inferred relationship Some
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. Is a True Intrahepatic cholestasis Inferred relationship Some
Cholestasis of parenteral nutrition (disorder) Is a True Intrahepatic cholestasis Inferred relationship Some

This concept is not in any reference sets

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