Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3752667019 | Stewart-Morel-Morgagni syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 3752668012 | Stewart-Morel-Morgagni syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Stewart-Morel-Morgagni syndrome | Is a | Hyperostosis interna frontalis | true | Inferred relationship | Existential restriction modifier | ||
| Stewart-Morel-Morgagni syndrome | Finding site | Frontal bone structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Stewart-Morel-Morgagni syndrome | Is a | Disorder of skull | true | Inferred relationship | Existential restriction modifier | ||
| Stewart-Morel-Morgagni syndrome | Is a | Metabolic bone disease | true | Inferred relationship | Existential restriction modifier | ||
| Stewart-Morel-Morgagni syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
| Stewart-Morel-Morgagni syndrome | Associated morphology | Internal hyperostosis | true | Inferred relationship | Existential restriction modifier | 1 | |
| Stewart-Morel-Morgagni syndrome | Is a | Hypertrophy of bone | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR