Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2974838019 | Single congenital anomaly | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2974959010 | Single congenital anomaly (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3006500014 | Single congenital malformation | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Single congenital anomaly | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Single congenital anomaly | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Single congenital anomaly | Is a | Congenital anomaly | false | Inferred relationship | Some | ||
| Single congenital anomaly | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Single congenital anomaly | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | ||
| Single congenital anomaly | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Single congenital anomaly | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
| Single congenital anomaly | Is a | Congenital anomaly | 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
FHIR