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897539005: Congenital anomaly of cochlea (disorder)


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


4 descendants. Search Descendants:

Expanded Value Set


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

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