Status: current, 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 |
132070012 | Congenital hepatic fibrosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
820676011 | Congenital hepatic fibrosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
NPHP3-related Meckel-like syndrome | est un(e) (attribut) | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Congenital cystic disease of liver | est un(e) (attribut) | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Nephronophthisis hepatic fibrosis syndrome (disorder) | est un(e) (attribut) | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Joubert syndrome with congenital hepatic fibrosis (disorder) | est un(e) (attribut) | True | Congenital hepatic fibrosis | Inferred relationship | Some | |
Hepatic fibrosis, renal cyst, intellectual disability syndrome (disorder) | est un(e) (attribut) | True | Congenital hepatic fibrosis | Inferred relationship | Some |
Reference Sets