Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core
Descriptions:
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Cyst of intrahepatic bile ducts | Is a | True | Liver cyst | Inferred relationship | Some | |
Hepatic peliosis | Is a | False | Liver cyst | Inferred relationship | Some | |
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). | Is a | True | Liver cyst | Inferred relationship | Some | |
Fibropolycystic disease of liver | Is a | True | Liver cyst | Inferred relationship | Some | |
Congenital cystic disease of liver | Is a | True | Liver cyst | Inferred relationship | Some | |
Rupture of liver due to Echinococcus granulosus infection (disorder) | Is a | True | Liver cyst | Inferred relationship | Some | |
polykystose hépatique autosomique dominante | Is a | False | Liver cyst | Inferred relationship | Some | |
Peliosis hepatis | Is a | True | Liver cyst | Inferred relationship | Some |
This concept is not in any reference sets