Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2989856013 | Congenital velopharyngeal dysfunction (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2989902017 | Congenital velopharyngeal dysfunction | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital velopharyngeal dysfunction | Is a | Congenital disease | true | Inferred relationship | Some | ||
Congenital velopharyngeal dysfunction | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital velopharyngeal dysfunction | Is a | Velopharyngeal inadequacy | true | Inferred relationship | Some | ||
Congenital velopharyngeal dysfunction | Finding site | Muscle structure of pharynx | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital velopharyngeal incompetence | Is a | True | Congenital velopharyngeal dysfunction | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Queensland allied health clinical finding reference set
Clinical finding foundation reference set
Respiratory finding reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set