Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2787760013 | Hereditary factor IX deficiency disease with inhibitor (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
2791040019 | Haemophilia B with inhibitor | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2791041015 | Hemophilia B with inhibitor | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2791042010 | Hereditary factor IX deficiency disease with inhibitor | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary factor IX deficiency disease with inhibitor | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
Hereditary factor IX deficiency disease with inhibitor | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
Hereditary factor IX deficiency disease with inhibitor | Is a | Hereditary factor IX deficiency disease | true | Inferred relationship | Some | ||
Hereditary factor IX deficiency disease with inhibitor | Occurrence | Congenital | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Severe hereditary factor IX deficiency disease with inhibitor | Is a | True | Hereditary factor IX deficiency disease with inhibitor | Inferred relationship | Some | |
Mild hereditary factor IX deficiency disease with inhibitor | Is a | True | Hereditary factor IX deficiency disease with inhibitor | Inferred relationship | Some | |
Moderate hereditary factor IX deficiency disease with inhibitor | Is a | True | Hereditary factor IX deficiency disease with inhibitor | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set