Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 62317016 | Royer's syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 62319018 | Prader-Willi syndrome AND diabetes | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 769213011 | Royer's syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 2840034017 | Royer syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 1991961000005112 | Royers syndrom | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Royers syndrom | Is a | Multiple malformation syndrome with unusual brain and/or neuromuscular findings | false | Inferred relationship | Some | ||
| Royers syndrom | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Royers syndrom | Finding site | Brain structure | false | Inferred relationship | Some | 1 | |
| Royers syndrom | Associated morphology | Kongenit malformation | false | Inferred relationship | Some | ||
| Royers syndrom | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Royers syndrom | Associated morphology | dysgenese | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR