Status: current, Sufficiently defined by necessary conditions definition status. Date: 30-Nov 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5156368012 | Hereditary von Willebrand disease | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 5156369016 | Hereditary von Willebrand disease (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary von Willebrand disease | Is a | von Willebrand disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary von Willebrand disease | Is a | Autosomal hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary von Willebrand disease | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hereditary von Willebrand disease | Has interpretation | Abnormal | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary von Willebrand disease type 1 | Is a | True | Hereditary von Willebrand disease | Inferred relationship | Existential restriction modifier | |
| Hereditary von Willebrand disease type 2 | Is a | True | Hereditary von Willebrand disease | Inferred relationship | Existential restriction modifier | |
| Hereditary von Willebrand disease type 3 | Is a | True | Hereditary von Willebrand disease | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR