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1234911006: Congenital cochleovestibular malformation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5084709014 Congenital cochleovestibular malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5084710016 Congenital cochleovestibular malformation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5084711017 A rare otorhinolaryngological malformation with characteristics of varying degrees of malformation of the inner ear associated with severe to profound congenital sensorineural hearing loss in the absence of cochlear nerve anomalies (hypoplasia or aplasia). Categorisation of the malformation is based on the morphology of the cochlea, modiolus, and lamina cribrosa, which can range from normal development of these structures (with the malformation being limited to other structures of the inner ear) to their complete absence. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5084712012 A rare otorhinolaryngological malformation with characteristics of varying degrees of malformation of the inner ear associated with severe to profound congenital sensorineural hearing loss in the absence of cochlear nerve anomalies (hypoplasia or aplasia). Categorization of the malformation is based on the morphology of the cochlea, modiolus, and lamina cribrosa, which can range from normal development of these structures (with the malformation being limited to other structures of the inner ear) to their complete absence. 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 cochleovestibular malformation est un(e) (attribut) Decreased hearing true Inferred relationship Some
Congenital cochleovestibular malformation est un(e) (attribut) Congenital anomaly of ear with impairment of hearing true Inferred relationship Some
Congenital cochleovestibular malformation est un(e) (attribut) Congenital anomaly of inner ear true Inferred relationship Some
Congenital cochleovestibular malformation est un(e) (attribut) Congenital sensorineural hearing loss (disorder) true Inferred relationship Some
Congenital cochleovestibular malformation interprète (attribut) Hearing, function (observable entity) true Inferred relationship Some 2
Congenital cochleovestibular malformation a pour interprétation (attribut) Decreased true Inferred relationship Some 2
Congenital cochleovestibular malformation survenue (attribut) congénital true Inferred relationship Some 1
Congenital cochleovestibular malformation localisation d'une constatation (attribut) structure de l'oreille interne (structure corporelle) true Inferred relationship Some 1
Congenital cochleovestibular malformation morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Congenital cochleovestibular malformation Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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