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 |
| 194700017 | von Willebrand disease type 1 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 206396018 | Hereditary von Willebrand disease type 1 | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5156373018 | Hereditary von Willebrand disease type 1 (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 365491000146113 | ziekte van von Willebrand type 1 | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 365501000146115 | ziekte van von Willebrand type 1 (aandoening) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 5156372011 | A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). The type 1 disease is considered to be the most common form of VWD, caused by mutations in the VWF gene (12p13.3). Transmitted in an autosomal dominant manner. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary von Willebrand disease type 1 | Is a | von Willebrand disorder | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 1 | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 1 | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 1 | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 1 | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Hereditary von Willebrand disease type 1 | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hereditary von Willebrand disease type 1 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 1 | Is a | Hereditary von Willebrand disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary von Willebrand disease type 1C | Is a | True | Hereditary von Willebrand disease type 1 | Inferred relationship | Some | |
| Hereditary von Willebrand disease type 1B | Is a | True | Hereditary von Willebrand disease type 1 | Inferred relationship | Some | |
| Hereditary von Willebrand disease type 1A | Is a | True | Hereditary von Willebrand disease type 1 | Inferred relationship | Some |
This concept is not in any reference sets
FHIR