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 |
| 351270010 | vWD - Congenital von Willebrand's disease type I | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 351271014 | Congenital von Willebrand's disease type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 622766011 | Congenital von Willebrand's disease type I (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2841830016 | Congenital von Willebrand disease type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1944771000052118 | medfödd von Willebrands sjukdom, typ 1 | 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 |
| Congenital von Willebrand's disease type I | Is a | Congenital von Willebrand's disease | true | Inferred relationship | Some | ||
| Congenital von Willebrand's disease type I | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Congenital von Willebrand's disease type I | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital von Willebrand's disease type I | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Congenital von Willebrand's disease type I | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Congenital von Willebrand's disease type I | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
| Congenital von Willebrand's disease type I | Interprets | Hemostatic function | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR