Status: current, Defined. Date: 31-Jan 2015. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3034825014 | Congenital absence of eyelid | en | Synonym | Active | Case insensitive | SNOMED CT core |
3034841010 | Complete ablepharon | en | Synonym | Active | Case insensitive | SNOMED CT core |
3034852016 | Agenesis of eyelid | en | Synonym | Active | Case insensitive | SNOMED CT core |
3034859013 | Complete ablepharon (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Complete ablepharon | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Complete ablepharon | Associated morphology | Agenesis | true | Inferred relationship | Some | 1 | |
Complete ablepharon | Is a | Ablepharon | true | Inferred relationship | Some | ||
Complete ablepharon | Associated morphology | Congenital absence | false | Inferred relationship | Some | 1 | |
Complete ablepharon | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Complete ablepharon | Finding site | Entire eyelid | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set