Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 474908012 | von Willebrand disease Normandy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 734389013 | von Willebrand disease Normandy (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 1944941000052111 | von Willebrands sjukdom, typ 2N | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| von Willebrands sjukdom, typ 2N | Is a | von Willebrand disorder | false | Inferred relationship | Some | ||
| von Willebrands sjukdom, typ 2N | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| von Willebrands sjukdom, typ 2N | Finding site | Body system structure | false | Inferred relationship | Some | ||
| von Willebrands sjukdom, typ 2N | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR