Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4034274011 | Congenital anomaly of cochlea | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4034275012 | Congenital anomaly of cochlea (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5827621000241114 | anomalie congénitale de la cochlée | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5827631000241111 | anomalie congénitale cochléaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital anomaly of cochlea | Is a | Congenital anomaly of membranous labyrinth | true | Inferred relationship | Some | ||
Congenital anomaly of cochlea | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 1 | |
Congenital anomaly of cochlea | Finding site | Cochlear structure | true | Inferred relationship | Some | 1 | |
Congenital anomaly of cochlea | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital anomaly of cochlea | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital anomaly of cochlea | Is a | Congenital anomaly of vestibule of inner ear | false | Inferred relationship | Some | ||
Congenital anomaly of cochlea | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital anomaly of organ of Corti | Is a | True | Congenital anomaly of cochlea | Inferred relationship | Some | |
Incomplete formation of bony cochlea | Is a | True | Congenital anomaly of cochlea | Inferred relationship | Some | |
A rare otorhinolaryngological malformation characterised by a hypoplastic or absent cochlear nerve, resulting in variable hearing loss or total deafness, depending on the quantity of nerve fibres present. The condition can be unilateral or bilateral, occur as an isolated malformation or in the context of a complex syndrome, and may be associated with a hypoplastic internal auditory or cochlear nerve canal. | Is a | True | Congenital anomaly of cochlea | Inferred relationship | Some |
This concept is not in any reference sets