Status: current. Date: 30-Jun 2022
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 | Inactive | 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 | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400137018 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400138011 | 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 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. | 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 | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Is a | Autoimmune hepatitis (disorder) | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Finding site | Liver structure | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Pathological process (attribute) | Autoimmune process | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 2 | |
| Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome | Finding site | Biliary tract structure | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR