Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2995130013 | Dappled metaphysis syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3008581017 | Spondyloepimetaphyseal dysplasia, Strudwick type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3008635013 | Spondyloepimetaphyseal dysplasia, Strudwick type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 3008691019 | SEMD - spondyloepimetaphyseal dysplasia, Strudwick type | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3008722011 | Strudwick syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Spondyloepimetaphyseal dysplasia, Strudwick type | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Spondyloepimetaphyseal dysplasia, Strudwick type | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Spondyloepimetaphyseal dysplasia, Strudwick type | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Spondyloepimetaphyseal dysplasia, Strudwick type | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Spondyloepimetaphyseal dysplasia, Strudwick type | Is a | Osteochondrodysplasia syndrome | true | Inferred relationship | Some | ||
| Spondyloepimetaphyseal dysplasia, Strudwick type | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Spondyloepimetaphyseal dysplasia, Strudwick type | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR