Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3760123011 | Conductive hearing loss, malformation of external ear syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3760124017 | Conductive deafness, malformed external ear syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3760125016 | Mengel Konigsmark syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3760128019 | Conductive hearing loss, malformation of external ear syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3760129010 | A very rare syndromic genetic deafness with characteristics of mild to moderate conductive hearing loss, dysmorphic pinnae and lip pits or dimples. The pinnae are usually small, cup-shaped with helix folded forward, and hearing loss is associated with malformed ossicles and displacement of the external auditory canal. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Conductive deafness, malformed external ear syndrome | Is a | Congenital conductive hearing loss | true | Inferred relationship | Some | ||
Conductive deafness, malformed external ear syndrome | Interprets | Hearing | true | Inferred relationship | Some | 2 | |
Conductive deafness, malformed external ear syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Conductive deafness, malformed external ear syndrome | Finding site | External ear structure | true | Inferred relationship | Some | 1 | |
Conductive deafness, malformed external ear syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Conductive deafness, malformed external ear syndrome | Is a | Congenital abnormality of external ear | true | Inferred relationship | Some | ||
Conductive deafness, malformed external ear syndrome | Has interpretation | Decreased | true | Inferred relationship | Some | 2 | |
Conductive deafness, malformed external ear syndrome | Is a | Genetic disease | true | Inferred relationship | Some | ||
Conductive deafness, malformed external ear syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set