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 |
351272019 | Congenital von Willebrand's disease type II | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
351273012 | vWD - Congenital von Willebrand's disease type II | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
622767019 | Congenital von Willebrand's disease type II (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2840382017 | Congenital von Willebrand disease type II | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
1944781000052116 | medfödd von Willebrands sjukdom, typ 2 | 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 II | Is a | Congenital von Willebrand's disease | true | Inferred relationship | Some | ||
Congenital von Willebrand's disease type II | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
Congenital von Willebrand's disease type II | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital von Willebrand's disease type II | Finding site | Body system structure | false | Inferred relationship | Some | ||
Congenital von Willebrand's disease type II | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
Congenital von Willebrand's disease type II | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Congenital von Willebrand's disease type II | Interprets | Hemostatic function | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets