Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 2790086014 | Mild hereditary factor IX deficiency disease with inhibitor (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core | 
| 2791292015 | Mild hemophilia B with inhibitor | en | Synonym | Active | Initial character case insensitive | SNOMED CT core | 
| 2793938017 | Mild hereditary factor IX deficiency disease with inhibitor | en | Synonym | Active | Initial character case insensitive | SNOMED CT core | 
| 2794994014 | Mild haemophilia B with inhibitor | en | Synonym | Active | Initial character case insensitive | SNOMED CT core | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Mild hereditary factor IX deficiency disease with inhibitor | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Mild hereditary factor IX deficiency disease with inhibitor | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Mild hereditary factor IX deficiency disease with inhibitor | Is a | Hereditary factor IX deficiency disease with inhibitor | true | Inferred relationship | Some | ||
| Mild hereditary factor IX deficiency disease with inhibitor | Occurrence | Congenital | true | Inferred relationship | Some | 2 | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set