Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 373313011 | White blood cell chromosome abnormality | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 640820012 | White blood cell chromosome abnormality (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| White blood cell chromosome abnormality | Interprets | White blood cell test | true | Inferred relationship | Some | 1 | |
| White blood cell chromosome abnormality | Finding site | Leucocyte | false | Inferred relationship | Some | ||
| White blood cell chromosome abnormality | Interprets | Laboratory test | false | Inferred relationship | Some | ||
| White blood cell chromosome abnormality | Finding method | Procedure | false | Inferred relationship | Some | ||
| White blood cell chromosome abnormality | Interprets | Haematology procedure | false | Inferred relationship | Some | 1 | |
| White blood cell chromosome abnormality | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| White blood cell chromosome abnormality | Is a | White blood cell finding | 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