Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3752667019 | Stewart-Morel-Morgagni syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3752668012 | Stewart-Morel-Morgagni syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Stewart-Morel-Morgagni syndrome | Is a | Hyperostosis interna frontalis | true | Inferred relationship | Some | ||
Stewart-Morel-Morgagni syndrome | Finding site | Frontal bone structure | true | Inferred relationship | Some | 1 | |
Stewart-Morel-Morgagni syndrome | Is a | Disorder of skull | true | Inferred relationship | Some | ||
Stewart-Morel-Morgagni syndrome | Is a | Metabolic bone disease | true | Inferred relationship | Some | ||
Stewart-Morel-Morgagni syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Stewart-Morel-Morgagni syndrome | Associated morphology | Internal hyperostosis | true | Inferred relationship | Some | 1 | |
Stewart-Morel-Morgagni syndrome | Is a | Hypertrophy of bone | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set