Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2788310019 | Carrier of hereditary factor IX deficiency disease (finding) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
2790727011 | Haemophilia B carrier | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2790728018 | Hemophilia B carrier | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2794700018 | Carrier of hereditary factor IX deficiency disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Carrier of hereditary factor IX deficiency disease | Is a | Haemophilia carrier | true | Inferred relationship | Some | ||
Carrier of hereditary factor IX deficiency disease | Interprets | General clinical state | 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