Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 378509019 | Balanced rearrangement and structural marker | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 645145010 | Balanced rearrangement and structural marker (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Balanced rearrangement and structural marker | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Balanced rearrangement and structural marker | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| Balanced rearrangement and structural marker | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | ||
| Balanced rearrangement and structural marker | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| Balanced rearrangement and structural marker | Is a | Chromosomal disorder | true | Inferred relationship | Some | ||
| Balanced rearrangement and structural marker | Finding site | Chromosome structure | true | Inferred relationship | Some | 1 | |
| Balanced rearrangement and structural marker | Associated morphology | Alteration of chromosome structure | false | Inferred relationship | Some | ||
| Balanced rearrangement and structural marker | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Balanced rearrangement and structural marker | Is a | Congenital chromosomal disease | false | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR