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