Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 101594016 | Congenital vascular disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 498945016 | Congenital vascular abnormality | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 498946015 | VM - Vascular malformation | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 498947012 | Vascular malformation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 800165017 | Congenital vascular disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital vascular disease | est un(e) (attribut) | Congenital anomaly of cardiovascular system | false | Inferred relationship | Some | ||
| Congenital vascular disease | est un(e) (attribut) | Disorder of blood vessel (disorder) | false | Inferred relationship | Some | ||
| Congenital vascular disease | localisation d'une constatation (attribut) | Cardiovascular system subdivision | false | Inferred relationship | Some | 2 | |
| Congenital vascular disease | localisation d'une constatation (attribut) | Blood vessel structure (body structure) | false | Inferred relationship | Some | 1 | |
| Congenital vascular disease | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Congenital vascular disease | morphologie associée (attribut) | Congenital anomaly | false | Inferred relationship | Some | 1 |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR