Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 123149016 | Progressive intrahepatic cholestasis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 123151017 | Familial intrahepatic cholestasis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 123152012 | Fatal intrahepatic cholestasis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4570357019 | Progressive familial intrahepatic cholestasis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4570358012 | PFIC - progressive familial intrahepatic cholestasis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 814631018 | Progressive intrahepatic cholestasis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Progressive familial intrahepatic cholestasis type 2 (disorder) | est un(e) (attribut) | True | Progressive intrahepatic cholestasis | Inferred relationship | Some | |
| Progressive familial intrahepatic cholestasis type 1 (disorder) | est un(e) (attribut) | True | Progressive intrahepatic cholestasis | Inferred relationship | Some | |
| Progressive familial intrahepatic cholestasis type 3 | est un(e) (attribut) | True | Progressive intrahepatic cholestasis | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set
FHIR