Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2018. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3527478013 | Congenital conductive hearing loss | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3527479017 | Congenital conductive hearing loss (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Facial dysmorphism, conductive hearing loss, heart defect syndrome | Is a | True | Congenital conductive hearing loss | Inferred relationship | Existential restriction modifier | |
Conductive hearing loss, malformation of external ear syndrome | Is a | True | Congenital conductive hearing loss | Inferred relationship | Existential restriction modifier | |
Multiple epiphyseal dysplasia Beighton type | Is a | True | Congenital conductive hearing loss | Inferred relationship | Existential restriction modifier | |
Johnson neuroectodermal syndrome | Is a | True | Congenital conductive hearing loss | Inferred relationship | Existential restriction modifier | |
Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome | Is a | True | Congenital conductive hearing loss | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets