Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4033155015 | Congenital epignathus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital epignathus (disorder) | Is a | Congenital anomaly of head | false | Inferred relationship | Some | ||
| Congenital epignathus (disorder) | Finding site | Head structure | true | Inferred relationship | Some | 1 | |
| Congenital epignathus (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital epignathus (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 | |
| Congenital epignathus (disorder) | Associated morphology | Teratoma - category | false | Inferred relationship | Some | 1 | |
| Congenital epignathus (disorder) | Is a | Epignathus | true | Inferred relationship | Some | ||
| Congenital epignathus (disorder) | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Congenital epignathus (disorder) | Associated morphology | Teratoma | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR