Status: current, Not 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 |
293528019 | Cystic fibrosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
293529010 | CF - Cystic fibrosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
293530017 | Fibrocystic disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
293532013 | Mucoviscidosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
574544017 | Cystic fibrosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cystic fibrosis | Is a | Disorder of respiratory system (disorder) | false | Inferred relationship | Some | ||
Cystic fibrosis | Is a | Inherited mucociliary clearance defect | true | Inferred relationship | Some | ||
Cystic fibrosis | Finding site | Structure of respiratory system (body structure) | 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 | false | Inferred relationship | Some | 2 | |
Cystic fibrosis | Finding site | Respiratory tract structure | true | Inferred relationship | Some | 2 | |
Cystic fibrosis | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some |
This concept is not in any reference sets