Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1769237019 | Smith-Magenis syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 1780502018 | Smith-Magenis syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Smith-Magenis syndrome | Is a | Multiple system malformation syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Smith-Magenis syndrome | Associated morphology | Congenital malformation | false | Inferred relationship | Existential restriction modifier | ||
| Smith-Magenis syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Smith-Magenis syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Smith-Magenis syndrome | Associated morphology | Developmental anomaly | false | Inferred relationship | Existential restriction modifier | 1 | |
| Smith-Magenis syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Smith-Magenis syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR