Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 194707019 | von Willebrand disease type IB | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 206399013 | Hereditary von Willebrand disease type IB | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3891029013 | Hereditary von Willebrand disease type 1B | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 5156378010 | Hereditary von Willebrand disease type 1B (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| von Willebrand disease type IB | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| von Willebrand disease type IB | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| von Willebrand disease type IB | Is a | von Willebrand disease type 1 | true | Inferred relationship | Some | ||
| von Willebrand disease type IB | Is a | von Willebrand disease type 2A | false | Inferred relationship | Some | ||
| von Willebrand disease type IB | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| von Willebrand disease type IB | Finding site | Body system structure | false | Inferred relationship | Some | ||
| von Willebrand disease type IB | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| von Willebrand disease type IB | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR