Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 194702013 | von Willebrand disease type 3 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 206398017 | Hereditary von Willebrand disease type 3 | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 732069015 | von Willebrand disease type 3 (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 1945011000052110 | von Willebrands sjukdom, typ 3 | sv | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| von Willebrand disease type 3 | Is a | von Willebrand disorder | true | Inferred relationship | Some | ||
| von Willebrand disease type 3 | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| von Willebrand disease type 3 | Finding site | Body system structure | false | Inferred relationship | Some | ||
| von Willebrand disease type 3 | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| von Willebrand disease type 3 | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| von Willebrand disease type 3 | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| von Willebrand disease type 3 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR