Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 474895016 | von Willebrand disease type 2N | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 5156384013 | Hereditary von Willebrand disease type 2N (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 5156385014 | Hereditary von Willebrand disease type 2N | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| von Willebrand disease type 2N | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| von Willebrand disease type 2N | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| von Willebrand disease type 2N | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| von Willebrand disease type 2N | Is a | von Willebrand disease type 2 | true | Inferred relationship | Some | ||
| von Willebrand disease type 2N | Is a | von Willebrand disorder | false | Inferred relationship | Some | ||
| von Willebrand disease type 2N | Finding site | Body system structure | false | Inferred relationship | Some | ||
| von Willebrand disease type 2N | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| von Willebrand disease type 2N | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| von Willebrand Normandy screening test | Has focus | True | von Willebrand disease type 2N | Inferred relationship | Some | 2 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR