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370489002: Cholangiohepatitis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1195782014 Cholangiohepatitis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1209223011 Cholangiohepatitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1375301000005110 kolangiohepatit da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cholangiohepatitis (disorder) Is a Inflammatory disease of liver true Inferred relationship Some
Cholangiohepatitis (disorder) Is a Cholangitis true Inferred relationship Some
Cholangiohepatitis (disorder) Finding site Structure of biliary tree (body structure) true Inferred relationship Some 2
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 2
Cholangiohepatitis (disorder) Finding site Liver structure true Inferred relationship Some 1
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 1
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 1
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 2
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 2
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 1
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 2
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 1
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 2
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 1
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 1
Cholangiohepatitis (disorder) Associated morphology Inflammation false Inferred relationship Some 2
Cholangiohepatitis (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 2
Cholangiohepatitis (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Primary sclerosing cholangitis Is a False Cholangiohepatitis (disorder) Inferred relationship Some
Cholangiolitis Is a True Cholangiohepatitis (disorder) Inferred relationship Some
Orientalsk kolangiohepatit Is a False Cholangiohepatitis (disorder) Inferred relationship Some
Cholangitis-cholangiohepatitis syndrome in cats Is a False Cholangiohepatitis (disorder) Inferred relationship Some
Chronic lymphocytic cholangitis-cholangiohepatitis Is a True Cholangiohepatitis (disorder) Inferred relationship Some
Acute cholangiohepatitis (disorder) Is a True Cholangiohepatitis (disorder) Inferred relationship Some
Cholestatic hepatitis Is a True Cholangiohepatitis (disorder) Inferred relationship Some
Primary biliary cholangitis Is a True Cholangiohepatitis (disorder) Inferred relationship Some
Intrahepatic cholangitis due to intrahepatic cholelithiasis Is a True Cholangiohepatitis (disorder) Inferred relationship Some
A rare hepatic disease characterized by the overlap of primary biliary cholangitis and/or primary sclerosing cholangitis with autoimmune hepatitis, defined by the presence of at least two of the three recognized biochemical, serological, and histological criteria of each disease. The onset of the overlapping diseases can be simultaneous or sequential, with a variable interval of up to several years. Age of onset, gender predisposition, and clinical phenotype vary between each of the diseases, and the clinical presentation ranges from asymptomatic disease or unspecific symptoms such as fatigue, arthralgia, and pruritus, to established cirrhosis and decompensation, or also acute, fulminant hepatitis and liver failure. Association with extrahepatic autoimmune diseases is common. Is a True Cholangiohepatitis (disorder) Inferred relationship Some

Reference Sets

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