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 |
| 194701018 | von Willebrand disease type 2 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 206397010 | Hereditary von Willebrand disease type 2 | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5156380016 | Hereditary von Willebrand disease type 2 (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5156383019 | A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive. | 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 2 | Is a | von Willebrand disorder | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 2 | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 2 | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 2 | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 2 | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Hereditary von Willebrand disease type 2 | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hereditary von Willebrand disease type 2 | Is a | Autosomal hereditary disorder | false | Inferred relationship | Some | ||
| Hereditary von Willebrand disease type 2 | Is a | Hereditary von Willebrand disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary von Willebrand disease type 2N (disorder) | Is a | True | Hereditary von Willebrand disease type 2 | Inferred relationship | Some | |
| Hereditary von Willebrand disease type 2A | Is a | True | Hereditary von Willebrand disease type 2 | Inferred relationship | Some | |
| Hereditary von Willebrand disease type 2B | Is a | True | Hereditary von Willebrand disease type 2 | Inferred relationship | Some | |
| Hereditary von Willebrand disease type 2M | Is a | True | Hereditary von Willebrand disease type 2 | Inferred relationship | Some |
This concept is not in any reference sets
FHIR