1234911006: Congenital cochleovestibular malformation (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of head region\Ear finding (finding)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Head finding (finding)\Finding of head region\Ear finding (finding)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Head finding (finding)\Finding of head region\Ear finding (finding)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)

\Ear, nose and throat finding\Ear finding (finding)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Ear, nose and throat finding\Ear finding (finding)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Ear, nose and throat finding\Ear finding (finding)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Ear, nose and throat finding\affection de l'oreille, du nez et de la gorge\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Ear, nose and throat finding\affection de l'oreille, du nez et de la gorge\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Ear, nose and throat finding\affection de l'oreille, du nez et de la gorge\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)

\Ear and auditory finding\Disorder of auditory system\Hearing disorder (disorder)\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Disorder of auditory system\Hearing disorder (disorder)\Congenital hearing disorder\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Disorder of auditory system\Hearing disorder (disorder)\Hearing loss\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Disorder of auditory system\Hearing disorder (disorder)\Hearing loss\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Disorder of auditory system\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Disorder of auditory system\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Disorder of auditory system\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Ear finding (finding)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Ear finding (finding)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Ear finding (finding)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Hearing finding\Hearing disorder (disorder)\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Hearing finding\Hearing disorder (disorder)\Congenital hearing disorder\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Hearing finding\Hearing disorder (disorder)\Hearing loss\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Hearing finding\Hearing disorder (disorder)\Hearing loss\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Ear and auditory finding\Hearing finding\Decreased hearing\Congenital cochleovestibular malformation (disorder)

\Functional finding\Decline in functional status (finding)\Decreased hearing\Congenital cochleovestibular malformation (disorder)
\Functional finding\Hearing finding\Hearing disorder (disorder)\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Functional finding\Hearing finding\Hearing disorder (disorder)\Congenital hearing disorder\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Functional finding\Hearing finding\Hearing disorder (disorder)\Hearing loss\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Functional finding\Hearing finding\Hearing disorder (disorder)\Hearing loss\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Functional finding\Hearing finding\Decreased hearing\Congenital cochleovestibular malformation (disorder)

\Disease\Disorder of sensory organ (disorder)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of sensory organ (disorder)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of sensory organ (disorder)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital hearing disorder\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder (disorder)\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder (disorder)\Congenital hearing disorder\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder (disorder)\Hearing loss\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder (disorder)\Hearing loss\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of body system\Disorder of auditory system\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\affection de l'oreille, du nez et de la gorge\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\affection de l'oreille, du nez et de la gorge\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\affection de l'oreille, du nez et de la gorge\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of head (disorder)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of head (disorder)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\Disorder of head (disorder)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear\Congenital cochleovestibular malformation (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of ear with impairment of hearing\Congenital cochleovestibular malformation (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of inner ear\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

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

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

3387151001000116 Dysplasie, kochleovestibuläre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3387151001000116 Dysplasie, kochleovestibuläre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital cochleovestibular malformation (disorder)	Is a	Decreased hearing	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital cochleovestibular malformation (disorder)	Is a	Congenital anomaly of ear with impairment of hearing	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital cochleovestibular malformation (disorder)	Is a	Congenital anomaly of inner ear	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital cochleovestibular malformation (disorder)	Is a	Congenital sensorineural hearing loss (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital cochleovestibular malformation (disorder)	Interprets	Hearing	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital cochleovestibular malformation (disorder)	Has interpretation	Decreased	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital cochleovestibular malformation (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital cochleovestibular malformation (disorder)	Finding site	Inner ear structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital cochleovestibular malformation (disorder)	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital cochleovestibular malformation (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

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

Back to Start

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
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
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
3387151001000116	Dysplasie, kochleovestibuläre	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3387151001000116	Dysplasie, kochleovestibuläre	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module