Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
132070012 | Congenital hepatic fibrosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
820676011 | Congenital hepatic fibrosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
NPHP3-related Meckel-like syndrome | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Congenital cystic disease of liver | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Caroli syndrome | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Boichis syndrome | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Joubert syndrome with hepatic defect | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Hepatic fibrosis, renal cyst, intellectual disability syndrome | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set