43353004: Congenital anomaly of inner ear (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 inner ear
\Head finding (finding)\Finding of head region\Ear finding (finding)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear
\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital malformation of ear\Congenital anomaly of inner ear
\Head finding (finding)\Disorder of head (disorder)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear
\Head finding (finding)\Disorder of head (disorder)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear

\Ear, nose and throat finding\Ear finding (finding)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear
\Ear, nose and throat finding\Ear finding (finding)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear
\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
\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

\Ear and auditory finding\Disorder of auditory system\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear
\Ear and auditory finding\Disorder of auditory system\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear
\Ear and auditory finding\Ear finding (finding)\Disorder of ear\Congenital malformation of ear\Congenital anomaly of inner ear
\Ear and auditory finding\Ear finding (finding)\Disorder of ear\Disorder of inner ear (disorder)\Congenital anomaly of inner ear

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

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital anomaly of inner ear	Is a	Congenital anomaly of ear	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital anomaly of inner ear	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital anomaly of inner ear	Finding site	Inner ear structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of inner ear	Is a	Disorder of inner ear (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital anomaly of inner ear	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of inner ear	Finding site	Inner ear structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of inner ear	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of inner ear	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital anomaly of inner ear	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital anomaly of inner ear	Finding site	Inner ear structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital anomaly of inner ear	Is a	Congenital malformation of ear	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital anomaly of inner ear	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of inner ear	Finding site	Inner ear structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of inner ear	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of inner ear	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
Congenital aplasia of inner ear	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Neurofibromatosis type 2	Is a	False	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital abnormal shape of inner ear	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital deafness	Is a	False	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Hutchinson's triad	Is a	False	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Structural anomaly of the cochlea and vestibular labyrinth	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Vascular malformation of inner ear	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital anomaly of membranous labyrinth (disorder)	Is a	False	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Inner ear anomalies NOS	Is a	False	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Deafness, vitiligo, achalasia syndrome	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital deafness with labyrinthine aplasia, microtia and microdontia	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare genetic hematologic disorder characterized by bone marrow failure which manifests with aplastic anemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner. Caused by heterozygous mutation in the SRP72 gene on chromosome 4q12.	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Neutropenia, monocytopenia, deafness syndrome (disorder)	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Sinoatrial node dysfunction and deafness (disorder)	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital cochleovestibular malformation (disorder)	Is a	True	Congenital anomaly of inner ear	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
72332012	Congenital anomaly of inner ear	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
780355017	Congenital anomaly of inner ear (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3006548010	Congenital malformation of inner ear	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3787195019	Congenital abnormality of inner ear	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
72332012	Congenital anomaly of inner ear	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
72332012	Congenital anomaly of inner ear	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
780355017	Congenital anomaly of inner ear (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
780355017	Congenital anomaly of inner ear (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3006548010	Congenital malformation of inner ear	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3006548010	Congenital malformation of inner ear	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3787195019	Congenital abnormality of inner ear	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
390581000274119	Angeborene Fehlbildung des Innenohres	de	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5989471000241116	anomalie congénitale de l'oreille interne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5989471000241116	anomalie congénitale de l'oreille interne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
390581000274119	Angeborene Fehlbildung des Innenohres	de	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module