Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1225870016 | Congenital factor VIII deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2787090010 | Hereditary factor VIII deficiency disease (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 47356012 | Hemophilia A | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 47359017 | Hereditary factor VIII deficiency disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 47360010 | Classical hemophilia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 47361014 | AHG deficiency disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 47362019 | Sex-linked factor VIII deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 47363012 | Congenital factor VIII deficiency disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 483814018 | Haemophilia A | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 483815017 | Classical haemophilia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary factor VIII deficiency disease | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Hereditary factor VIII deficiency disease | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hereditary factor VIII deficiency disease | Is a | X-linked hereditary disease | true | Inferred relationship | Some | ||
| Hereditary factor VIII deficiency disease | Is a | Haemophilia | true | Inferred relationship | Some | ||
| Hereditary factor VIII deficiency disease | Is a | Hereditary coagulation factor deficiency | true | Inferred relationship | Some | ||
| Hereditary factor VIII deficiency disease | Is a | Factor VIII deficiency | true | Inferred relationship | Some | ||
| Hereditary factor VIII deficiency disease | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary factor VIII deficiency disease | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Hereditary factor VIII deficiency disease | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Severe hereditary factor VIII deficiency disease | Is a | True | Hereditary factor VIII deficiency disease | Inferred relationship | Some | |
| Mild hereditary factor VIII deficiency disease | Is a | True | Hereditary factor VIII deficiency disease | Inferred relationship | Some | |
| Moderate hereditary factor VIII deficiency disease | Is a | True | Hereditary factor VIII deficiency disease | Inferred relationship | Some | |
| Hereditary factor VIII deficiency disease without inhibitor | Is a | True | Hereditary factor VIII deficiency disease | Inferred relationship | Some | |
| Carrier of hereditary factor VIII deficiency disease | Is a | False | Hereditary factor VIII deficiency disease | Inferred relationship | Some | |
| Hereditary factor VIII deficiency disease with inhibitor | Is a | True | Hereditary factor VIII deficiency disease | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR