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1186656004: congenitale aplasie of hypoplasie van nervus cochlearis (aandoening)


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


0 descendants.

Expanded Value Set


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

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