Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3004456012 | Congenital osteodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 45771000119115 | Congenital osteodystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital osteodystrophy | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Congenital osteodystrophy | Is a | Osteodystrophy | true | Inferred relationship | Some | ||
| Congenital osteodystrophy | Is a | Disorder of bone | false | Inferred relationship | Some | ||
| Congenital osteodystrophy | Is a | Degenerative disorder | false | Inferred relationship | Some | ||
| Congenital osteodystrophy | Is a | Congenital connective tissue disorder | false | Inferred relationship | Some | ||
| Congenital osteodystrophy | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital osteodystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
| Congenital osteodystrophy | Finding site | Bone structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Francois syndrome | Is a | True | Congenital osteodystrophy | Inferred relationship | Some | |
| Morquio syndrome | Is a | True | Congenital osteodystrophy | Inferred relationship | Some | |
| DOORS syndrome | Is a | True | Congenital osteodystrophy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set
FHIR