1234911006: Congenital cochleovestibular malformation (disorder)

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

13660901000172113 congenitale cochleovestibulaire malformatie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

13660911000172111 aangeboren cochleovestibulaire misvorming nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

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

Characteristic

Refinability

This concept is not in any reference sets

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
13660901000172113	congenitale cochleovestibulaire malformatie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
13660911000172111	aangeboren cochleovestibulaire misvorming	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)