Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 351278015 | Acquired von Willebrand's disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1784908015 | Acquired von Willebrand syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1784909011 | Acquired von Willebrand disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5156395019 | Acquired von Willebrand disease (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5156397010 | Acquired von Willebrand disease (VWD) is a rare bleeding disorder marked by the same biological anomalies as those seen in hereditary von Willebrand disease (VWD) but which occurs in association with another underlying pathology, generally in elderly patients without any personal or family history of bleeding anomalies. There are three principle pathogenic mechanisms described which are firstly the presence of autoantibodies (inhibiting or noninhibiting) that form immune complexes with the von Willebrand factor (VWF) leading to rapid clearance of VWF from the circulation. Secondly, absorption of VWF onto malignant cell clones and thirdly the increased proteolysis of high molecular weight VWF multimers under abnormal blood conditions caused by cardiovascular malformations (such as aortic valve stenosis). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4995621000241112 | maladie de von Willebrand acquise | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Acquired von Willebrand disease | Is a | von Willebrand disorder | true | Inferred relationship | Some | ||
| Acquired von Willebrand disease | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Acquired von Willebrand disease | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Acquired von Willebrand disease | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Acquired von Willebrand disease | Occurrence | Period of life beginning after birth and ending before death (qualifier value) | true | Inferred relationship | Some | 1 | |
| Acquired von Willebrand disease | Is a | Acquired coagulation disorder | true | Inferred relationship | Some | ||
| Acquired von Willebrand disease | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
| Acquired von Willebrand disease | Interprets | Hemostatic function | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| von Willebrand factor inhibitor disorder | Is a | True | Acquired von Willebrand disease | Inferred relationship | Some |
This concept is not in any reference sets
FHIR