Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3638525019 | Isolated congenital maxillomandibular fusion | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3638526018 | Isolated congenital syngnathia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3638527010 | Isolated congenital syngnathia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3638528017 | A very rare developmental defect during embryogenesis with characteristics of varying degrees of congenital fusion (ranging from simple mucosal adhesions to extensive bony fusion) of mandible to maxilla that is not associated with any other malformations. Patients present with mouth opening limitation (which could range from severe to minimal restriction) that typically results in feeding, swallowing and/or respiratory difficulties that may lead to failure to thrive, malnutrition and/or temporomandibular joint ankylosis. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Isolated congenital syngnathia | Is a | Congenital anomaly of jaw | true | Inferred relationship | Some | ||
| Isolated congenital syngnathia | Associated morphology | Congenital abnormal fusion | true | Inferred relationship | Some | 1 | |
| Isolated congenital syngnathia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Isolated congenital syngnathia | Finding site | Jaw region structure | true | Inferred relationship | Some | 1 | |
| Isolated congenital syngnathia | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Isolated congenital syngnathia | Is a | Lesion of face | 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