Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 158711011 | Congenital deafness | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 512317011 | Congenital sensorineural deafness | en | Synonym | Inactive | Case insensitive | SNOMED CT core |
| 840063013 | Congenital deafness (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal dominant aplasia and myelodysplasia | Is a | True | Congenital deafness | Inferred relationship | Some | |
| Congenital prelingual deafness | Is a | True | Congenital deafness | Inferred relationship | Some | |
| Neutropenia, monocytopenia, deafness syndrome | Is a | True | Congenital deafness | Inferred relationship | Some | |
| Deafness, vitiligo, achalasia syndrome | Is a | True | Congenital deafness | Inferred relationship | Some | |
| Congenital deafness with labyrinthine aplasia, microtia and microdontia | Is a | True | Congenital deafness | Inferred relationship | Some | |
| Sinoatrial node dysfunction and deafness | Is a | True | Congenital deafness | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set