Status: retired, Primitive. Date: 31-Jul 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 474907019 | Hereditary von Willebrand disease type 2N | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 474908012 | von Willebrand disease Normandy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 734389013 | von Willebrand disease Normandy (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| von Willebrand disease Normandy | Is a | von Willebrand disorder | false | Inferred relationship | Some | ||
| von Willebrand disease Normandy | Finding site | Body system structure | false | Inferred relationship | Some | ||
| von Willebrand disease Normandy | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| von Willebrand disease Normandy | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set
FHIR