Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1495080011 | McLeod syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 351207014 | Blood group deletion syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 622726012 | Blood group deletion syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Blood group deletion syndrome | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| Blood group deletion syndrome | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Some | ||
| Blood group deletion syndrome | Is a | Erythrocyte membrane abnormality | true | Inferred relationship | Some | ||
| Blood group deletion syndrome | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| Blood group deletion syndrome | Finding site | Erythrocyte | 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