Status: current, Primitive. Date: 31-Jan 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3636279017 | Classical cystic fibrosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3636280019 | Classical cystic fibrosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Classical cystic fibrosis | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Classical cystic fibrosis | Is a | Cystic fibrosis | true | Inferred relationship | Some | ||
Classical cystic fibrosis | Is a | Hereditary disorder by system | false | Inferred relationship | Some | ||
Classical cystic fibrosis | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
Classical cystic fibrosis | Interprets | Mucociliary clearance | true | Inferred relationship | Some | 2 | |
Classical cystic fibrosis | Associated morphology | Defect | true | Inferred relationship | Some | 3 | |
Classical cystic fibrosis | Finding site | Respiratory tract structure | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Liver cirrhosis due to classical cystic fibrosis | Due to | True | Classical cystic fibrosis | Inferred relationship | Some | 4 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Respiratory finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set