Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1771686011 | XXYY syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 1782770018 | XXYY syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| XXYY syndrome | Is a | Congenital chromosomal disease | true | Inferred relationship | Some | ||
| XXYY syndrome | Occurrence | Congenital | false | Inferred relationship | Some | ||
| XXYY syndrome | Associated morphology | Alteration of chromosome structure | false | Inferred relationship | Some | ||
| XXYY syndrome | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| XXYY syndrome | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| XXYY syndrome | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | ||
| XXYY syndrome | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| XXYY syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| XXYY syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| XXYY 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