Status: current, Defined. Date: 31-Jan 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
459490018 | Congenital conduction defect | en | Synonym | Active | Case insensitive | SNOMED CT core |
711876016 | Congenital conduction defect (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Jervell and Lange-Nielsen syndrome | Is a | True | Congenital conduction defect | Inferred relationship | Some | |
Congenital heart block | Is a | True | Congenital conduction defect | Inferred relationship | Some | |
Jervell and Lange-Nielson syndrome | Is a | False | Congenital conduction defect | Inferred relationship | Some | |
Congenital complete atrioventricular heart block | Is a | True | Congenital conduction defect | Inferred relationship | Some | |
Congenital incomplete atrioventricular heart block | Is a | True | Congenital conduction defect | Inferred relationship | Some | |
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome | Is a | True | Congenital conduction defect | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set