Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 210869010 | Blood group antigen A variant | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 210870011 | Weak A subgroup | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 210871010 | Blood group A variant | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 735526010 | Blood group A variant (finding) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Blood group A variant | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| Blood group A variant | Interprets | Laboratory test | false | Inferred relationship | Some | ||
| Blood group A variant | Finding method | Procedure | false | Inferred relationship | Some | ||
| Blood group A variant | Is a | Blood group A | true | Inferred relationship | Some | ||
| Blood group A variant | Interprets | Genetic test | true | Inferred relationship | Some | 2 | |
| Blood group A variant | Interprets | Blood transfusion test | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Blood group A>3< | Is a | True | Blood group A variant | Inferred relationship | Some | |
| Blood group A>x< | Is a | True | Blood group A variant | Inferred relationship | Some | |
| Blood group A>m< | Is a | True | Blood group A variant | Inferred relationship | Some | |
| Blood group A>y< | Is a | True | Blood group A variant | Inferred relationship | Some | |
| Blood group A>end< | Is a | True | Blood group A variant | Inferred relationship | Some | |
| Blood group A>el< | Is a | True | Blood group A variant | Inferred relationship | Some |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR