Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4033154016 | Congenital epignathus (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4033155015 | Congenital epignathus | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4033156019 | A very rare and life threatening intraoral teratoma, usually arising from the maxilla, mandible, palate or base of skull and invading the cranium, nasopharynx or oral cavity. Epignathus is more commonly seen in females, and presents with various manifestations including dyspnoea, cyanosis, cough, difficulty in sucking and swallowing, and rarely vomiting (due to swallowing difficulties). When large, they can lead to airway obstruction, asphyxia and death in the neonatal period. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 4033157011 | A very rare and life threatening intraoral teratoma, usually arising from the maxilla, mandible, palate or base of skull and invading the cranium, nasopharynx or oral cavity. Epignathus is more commonly seen in females, and presents with various manifestations including dyspnea, cyanosis, cough, difficulty in sucking and swallowing, and rarely vomiting (due to swallowing difficulties). When large, they can lead to airway obstruction, asphyxia and death in the neonatal period. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital epignathus | Is a | Congenital anomaly of head | false | Inferred relationship | Some | ||
| Congenital epignathus | Finding site | Structure of head | true | Inferred relationship | Some | 1 | |
| Congenital epignathus | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital epignathus | Pathological process | Pathological developmental process | false | Inferred relationship | Some | 1 | |
| Congenital epignathus | Associated morphology | Teratoma - category | false | Inferred relationship | Some | 1 | |
| Congenital epignathus | Is a | Epignathus | true | Inferred relationship | Some | ||
| Congenital epignathus | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Congenital epignathus | Associated morphology | Teratoma | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set
FHIR