Status: current, Defined. Date: 31-Jan 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3527478013 | Congenital conductive hearing loss | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3527479017 | Congenital conductive hearing loss (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Conductive deafness, malformed external ear syndrome | Is a | True | Congenital conductive hearing loss | Inferred relationship | Some | |
| Multiple epiphyseal dysplasia Beighton type | Is a | True | Congenital conductive hearing loss | Inferred relationship | Some | |
| Johnson neuroectodermal syndrome | Is a | True | Congenital conductive hearing loss | Inferred relationship | Some | |
| Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome | Is a | True | Congenital conductive hearing loss | Inferred relationship | Some | |
| Facial dysmorphism, conductive hearing loss, heart defect syndrome | Is a | True | Congenital conductive hearing loss | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set