Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
194708012 | von Willebrand disease type IC | en | Synonym | Active | Case sensitive | SNOMED CT core |
206400018 | Hereditary von Willebrand disease type IC | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3891027010 | Hereditary von Willebrand disease type 1C | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5156379019 | Hereditary von Willebrand disease type 1C (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 IC | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
von Willebrand disease type IC | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
von Willebrand disease type IC | Is a | von Willebrand disease type 1 | true | Inferred relationship | Some | ||
von Willebrand disease type IC | Is a | von Willebrand disease type 2M | false | Inferred relationship | Some | ||
von Willebrand disease type IC | Finding site | Body system structure | false | Inferred relationship | Some | ||
von Willebrand disease type IC | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
von Willebrand disease type IC | 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