Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3004456012 | Congenital osteodystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 45771000119115 | Congenital osteodystrophy (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 osteodystrophy | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
| Congenital osteodystrophy | est un(e) (attribut) | Osteodystrophy | true | Inferred relationship | Some | ||
| Congenital osteodystrophy | est un(e) (attribut) | Disorder of bone (disorder) | false | Inferred relationship | Some | ||
| Congenital osteodystrophy | est un(e) (attribut) | affection dégénérative | false | Inferred relationship | Some | ||
| Congenital osteodystrophy | est un(e) (attribut) | affection congénitale du tissu conjonctif | false | Inferred relationship | Some | ||
| Congenital osteodystrophy | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Congenital osteodystrophy | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Congenital osteodystrophy | localisation d'une constatation (attribut) | structure osseuse | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| syndrome de François | est un(e) (attribut) | True | Congenital osteodystrophy | Inferred relationship | Some | |
| Morquio syndrome | est un(e) (attribut) | True | Congenital osteodystrophy | Inferred relationship | Some | |
| Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder) | est un(e) (attribut) | True | Congenital osteodystrophy | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR