Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
123149016 | Progressive intrahepatic cholestasis | en | Synonym | Active | Case insensitive | SNOMED CT core |
123151017 | Familial intrahepatic cholestasis | en | Synonym | Active | Case insensitive | SNOMED CT core |
123152012 | Fatal intrahepatic cholestasis | en | Synonym | Active | Case insensitive | SNOMED CT core |
4570357019 | Progressive familial intrahepatic cholestasis | en | Synonym | Active | Case insensitive | SNOMED CT core |
4570358012 | PFIC - progressive familial intrahepatic cholestasis | en | Synonym | Active | Case sensitive | SNOMED CT core |
814631018 | Progressive intrahepatic cholestasis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4570359016 | A heterogeneous group of autosomal recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin. Three types of PFIC have been identified and are related to mutations in hepatocellular transport system genes involved in bile formation. Main clinical manifestations include cholestasis, pruritus and jaundice. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Progressive familial intrahepatic cholestasis type 2 | Is a | True | Progressive intrahepatic cholestasis | Inferred relationship | Some | |
Progressive familial intrahepatic cholestasis type 1 | Is a | True | Progressive intrahepatic cholestasis | Inferred relationship | Some | |
Progressive familial intrahepatic cholestasis type 3 | Is a | True | Progressive intrahepatic cholestasis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set