Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2787399015 | Hemophilia carrier (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 294330014 | Haemophilia carrier | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 294331013 | Hemophilia carrier | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 574985019 | Hemophilia carrier (disorder) | en | Fully specified name | Inactive | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Haemophilia carrier | Is a | Blood coagulation disorder | false | Inferred relationship | Some | ||
| Haemophilia carrier | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Haemophilia carrier | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Haemophilia carrier | Is a | Carrier of disorder | true | Inferred relationship | Some | ||
| Haemophilia carrier | Interprets | General clinical state | true | Inferred relationship | Some | 1 | |
| Haemophilia carrier | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Carrier of hereditary factor IX deficiency disease | Is a | True | Haemophilia carrier | Inferred relationship | Some | |
| Carrier of hereditary factor VIII deficiency disease | Is a | True | Haemophilia carrier | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR