Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5068767014 | Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5068768016 | Overlap syndrome of autoimmune liver disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5068769012 | Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5068770013 | A rare hepatic disease characterised 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 recognised 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. 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5068771012 | 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. 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Is a | Cholangiohepatitis (disorder) | true | Inferred relationship | Some | ||
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Is a | Autoimmune hepatitis (disorder) | true | Inferred relationship | Some | ||
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Finding site | Liver structure | true | Inferred relationship | Some | 1 | |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 1 | |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Finding site | Biliary tract structure | true | Inferred relationship | Some | 2 | |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR