Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 785719013 | Otocephalic syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 80275016 | Otocephalic syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 80276015 | Otocephaly | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 80277012 | Otocephalus | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Otocephalic syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Otocephalic syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Otocephalic syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
| Otocephalic syndrome | Associated morphology | Congenital malformation | false | Inferred relationship | Some | ||
| Otocephalic syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Otocephalic syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
| Otocephalic syndrome | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
| Otocephalic syndrome | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR