Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2995113011 | Der(22) syndrome due to 3:1 meiotic disjunction events | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2995222019 | Supernumerary der(22)t(11;22) syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2995585015 | Supernumerary derivative 22 chromosome syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2995681016 | Emanuel syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 2995820019 | Supernumerary der(22)t(11;22) syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2995830011 | Supernumerary der(22) syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Emanuel syndrome | Is a | Congenital chromosomal disease | true | Inferred relationship | Some | ||
| Emanuel syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Emanuel syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Emanuel syndrome | Finding site | Chromosome structure | 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
FHIR