Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 474837010 | von Willebrand disease type 2A | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 733701017 | von Willebrand disease type 2A (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 385221000146112 | ziekte van von Willebrand type 2A | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 385231000146114 | ziekte van von Willebrand type 2A (aandoening) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| ziekte van von Willebrand type 2A | Is a | congenitale ziekte van von Willebrand | false | Inferred relationship | Some | ||
| ziekte van von Willebrand type 2A | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| ziekte van von Willebrand type 2A | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| ziekte van von Willebrand type 2A | Finding site | Body system structure | false | Inferred relationship | Some | ||
| ziekte van von Willebrand type 2A | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| ziekte van von Willebrand type 2A | Interprets | Hemostatic function | false | Inferred relationship | Some | 1 | |
| ziekte van von Willebrand type 2A | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary von Willebrand disease type 1B | Is a | False | ziekte van von Willebrand type 2A | Inferred relationship | Some | |
| ziekte van von Willebrand type 2A subtype IIC | Is a | False | ziekte van von Willebrand type 2A | Inferred relationship | Some | |
| ziekte van von Willebrand type 2A subtype IIH | Is a | False | ziekte van von Willebrand type 2A | Inferred relationship | Some | |
| ziekte van von Willebrand type 2A subtype IID | Is a | False | ziekte van von Willebrand type 2A | Inferred relationship | Some | |
| ziekte van von Willebrand type 2A subtype IIE | Is a | False | ziekte van von Willebrand type 2A | Inferred relationship | Some | |
| ziekte van von Willebrand type 2A subtype IIG | Is a | False | ziekte van von Willebrand type 2A | Inferred relationship | Some | |
| ziekte van von Willebrand type 2A subtype IIA (aandoening) | Is a | False | ziekte van von Willebrand type 2A | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR