Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3701622017 | Congenital upper esophageal web | en | Synonym | Active | Case insensitive | SNOMED CT core |
3701623010 | Congenital upper esophageal web (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3701624016 | Congenital upper oesophageal web | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital upper oesophageal web | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital upper oesophageal web | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital upper oesophageal web | Finding site | Structure of upper third of oesophagus | true | Inferred relationship | Some | 1 | |
Congenital upper oesophageal web | Associated morphology | Congenital webbing | true | Inferred relationship | Some | 1 | |
Congenital upper oesophageal web | Is a | Congenital web of oesophagus | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set