Status: retired, Primitive. Date: 30-Nov 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2839593011 | Congenital von Willebrand disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
351268018 | Congenital von Willebrand's disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
351269014 | vWD - Congenital von Willebrand's disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
622765010 | Congenital von Willebrand's disease (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital von Willebrand's disease | Has interpretation | Abnormal | false | Inferred relationship | Some | 2 | |
Congenital von Willebrand's disease | Interprets | Haemostatic function | false | Inferred relationship | Some | 2 | |
Congenital von Willebrand's disease | Is a | Congenital disease | false | Inferred relationship | Some | ||
Congenital von Willebrand's disease | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Congenital von Willebrand's disease | Finding site | Body system structure | false | Inferred relationship | Some | ||
Congenital von Willebrand's disease | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
Congenital von Willebrand's disease | Is a | von Willebrand disorder | false | Inferred relationship | Some | ||
Congenital von Willebrand's disease | Finding site | Entire haematological system | false | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Concept inactivation indicator reference set
REPLACED BY association reference set