Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
293528019 | Cystic fibrosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
293529010 | CF - Cystic fibrosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
293530017 | Fibrocystic disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
293531018 | CF | en | Synonym | Active | Case sensitive | SNOMED CT core |
293532013 | Mucoviscidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
574544017 | Cystic fibrosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cystic fibrosis | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Cystic fibrosis | Is a | Respiratory disease | false | Inferred relationship | Some | ||
Cystic fibrosis | Is a | Inherited mucociliary clearance defect | true | Inferred relationship | Some | ||
Cystic fibrosis | Finding site | Structure of respiratory system | false | Inferred relationship | Some | ||
Cystic fibrosis | Has interpretation | Impaired | true | Inferred relationship | Some | 1 | |
Cystic fibrosis | Interprets | Mucociliary clearance | true | Inferred relationship | Some | 1 | |
Cystic fibrosis | Associated morphology | Defect | true | Inferred relationship | Some | 2 | |
Cystic fibrosis | Finding site | Respiratory tract structure | true | Inferred relationship | Some | 2 |
Reference Sets
Emergency department reference set
Australian emergency department reference set
NSW Emergency Department reference set
Clinical finding foundation reference set
Respiratory finding reference set
Emergency department diagnosis reference set
Problem/Diagnosis reference set