Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 474881019 | von Willebrand disease type 2M | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 734160018 | von Willebrand disease type 2M (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 989851000172118 | maladie de von Willebrand type 2M | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| maladie de von Willebrand type 2M | Is a | von Willebrand disorder | false | Inferred relationship | Some | ||
| maladie de von Willebrand type 2M | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| maladie de von Willebrand type 2M | Finding site | Body system structure | false | Inferred relationship | Some | ||
| maladie de von Willebrand type 2M | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| maladie de von Willebrand type 2M | Interprets | Hemostatic function | false | Inferred relationship | Some | 1 | |
| maladie de von Willebrand type 2M | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary von Willebrand disease type 1C | Is a | False | maladie de von Willebrand type 2M | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR