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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
5400237014 A rare otorhinolaryngological malformation characterized by 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
5400238016 A rare otorhinolaryngological malformation characterised by 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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital cochleovestibular malformation Is a Decreased hearing (finding) true Inferred relationship Some
Congenital cochleovestibular malformation Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Some
Congenital cochleovestibular malformation Is a Congenital anomaly of inner ear true Inferred relationship Some
Congenital cochleovestibular malformation Is a Congenital sensorineural hearing loss (disorder) true Inferred relationship Some
Congenital cochleovestibular malformation Interprets Hearing true Inferred relationship Some 2
Congenital cochleovestibular malformation Has interpretation Decreased true Inferred relationship Some 2
Congenital cochleovestibular malformation Occurrence Congenital true Inferred relationship Some 1
Congenital cochleovestibular malformation Finding site Inner ear structure (body structure) true Inferred relationship Some 1
Congenital cochleovestibular malformation Associated morphology Morphologically abnormal structure (morphologic abnormality) 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

Component annotation with string value reference set (foundation metadata concept)

GB English

US English

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