Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5072153018 | Correction of congenital anomaly of lower limb | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5072154012 | Correction of congenital anomaly of lower limb (procedure) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Correction of congenital anomaly of lower limb | est un(e) (attribut) | Correction of congenital anomaly (procedure) | true | Inferred relationship | Some | ||
| Correction of congenital anomaly of lower limb | a pour objet (attribut) | Congenital anomaly of lower limb | true | Inferred relationship | Some | 2 | |
| Correction of congenital anomaly of lower limb | méthode (attribut) | action : réparation | true | Inferred relationship | Some | 1 | |
| Correction of congenital anomaly of lower limb | est un(e) (attribut) | réparation chirurgicale d'un membre inférieur | true | Inferred relationship | Some | ||
| Correction of congenital anomaly of lower limb | Procedure site - Direct (attribute) | membre inférieur | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Repair of congenital pseudoarthrosis of tibia | est un(e) (attribut) | True | Correction of congenital anomaly of lower limb | Inferred relationship | Some | |
| Closure of cleft foot | est un(e) (attribut) | True | Correction of congenital anomaly of lower limb | Inferred relationship | Some | |
| Correction of congenital deformity of lower limb (procedure) | est un(e) (attribut) | True | Correction of congenital anomaly of lower limb | Inferred relationship | Some |
This concept is not in any reference sets
FHIR