Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4667221014 | Cochlear nerve deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4667225017 | Congenital deficiency of cochlear nerve (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4667226016 | Congenital deficiency of cochlear nerve | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
13243371000146110 | congenitale aplasie of hypoplasie van nervus cochlearis | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
13243381000146112 | congenitale deficiëntie van nervus cochlearis | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
13243391000146114 | congenitale aplasie of hypoplasie van nervus cochlearis (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
4667220010 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4667222019 | A rare otorhinolaryngological malformation characterized by a hypoplastic or absent cochlear nerve, resulting in variable hearing loss or total deafness, depending on the quantity of nerve fibers 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital deficiency of cochlear nerve (disorder) | Is a | Congenital anomaly of peripheral nerve | true | Inferred relationship | Some | ||
Congenital deficiency of cochlear nerve (disorder) | Is a | Congenital anomaly of nervous system of head/neck (disorder) | true | Inferred relationship | Some | ||
Congenital deficiency of cochlear nerve (disorder) | Is a | Cochlear nerve disorder | true | Inferred relationship | Some | ||
Congenital deficiency of cochlear nerve (disorder) | Is a | Congenital anomaly of cochlea | true | Inferred relationship | Some | ||
Congenital deficiency of cochlear nerve (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital deficiency of cochlear nerve (disorder) | Finding site | Structure of cochlear nerve | true | Inferred relationship | Some | 1 | |
Congenital deficiency of cochlear nerve (disorder) | Associated morphology | Maturation defect | true | Inferred relationship | Some | 1 | |
Congenital deficiency of cochlear nerve (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets