Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
132070012 | Congenital hepatic fibrosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
820676011 | Congenital hepatic fibrosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Nephronophthisis hepatic fibrosis syndrome | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Existential restriction modifier | |
Joubert syndrome with congenital hepatic fibrosis | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Existential restriction modifier | |
Hepatic fibrosis, renal cyst, intellectual disability syndrome | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Existential restriction modifier | |
Nephrocystin 3-related Meckel-like syndrome | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Existential restriction modifier | |
Congenital cystic disease of liver | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Existential restriction modifier | |
Caroli syndrome | Is a | True | Congenital hepatic fibrosis | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets