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43353004: Congenital anomaly of inner ear (disorder)


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

Descriptions:

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
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


27 descendants. Search Descendants:

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 Some
Congenital anomaly of inner ear Occurrence Congenital false Inferred relationship Some
Congenital anomaly of inner ear Finding site Inner ear structure false Inferred relationship Some 1
Congenital anomaly of inner ear Is a Disorder of inner ear true Inferred relationship Some
Congenital anomaly of inner ear Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital anomaly of inner ear Finding site Inner ear structure false Inferred relationship Some 1
Congenital anomaly of inner ear Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital anomaly of inner ear Occurrence Congenital false Inferred relationship Some 2
Congenital anomaly of inner ear Associated morphology anomalie du développement false Inferred relationship Some 2
Congenital anomaly of inner ear Finding site Inner ear structure false Inferred relationship Some 2
Congenital anomaly of inner ear Is a Congenital malformation of ear (disorder) true Inferred relationship Some
Congenital anomaly of inner ear Occurrence Congenital true Inferred relationship Some 1
Congenital anomaly of inner ear Finding site Inner ear structure true Inferred relationship Some 1
Congenital anomaly of inner ear Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Congenital anomaly of inner ear Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital aplasia of inner ear Is a True Congenital anomaly of inner ear Inferred relationship Some
Neurofibromatosis type 2 Is a False Congenital anomaly of inner ear Inferred relationship Some
Congenital abnormal shape of inner ear Is a True Congenital anomaly of inner ear Inferred relationship Some
Congenital deafness Is a False Congenital anomaly of inner ear Inferred relationship Some
Hutchinson's triad Is a False Congenital anomaly of inner ear Inferred relationship Some
Structural anomaly of the cochlea and vestibular labyrinth Is a True Congenital anomaly of inner ear Inferred relationship Some
Vascular malformation of inner ear Is a True Congenital anomaly of inner ear Inferred relationship Some
Congenital anomaly of membranous labyrinth Is a False Congenital anomaly of inner ear Inferred relationship Some
Inner ear anomalies NOS Is a False Congenital anomaly of inner ear Inferred relationship Some
Deafness-vitiligo-achalasia syndrome is characterized by the association of deafness, short stature, vitiligo, muscle wasting, and achalasia. Is a True Congenital anomaly of inner ear Inferred relationship Some
Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome. Is a True Congenital anomaly of inner ear Inferred relationship Some
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. Is a True Congenital anomaly of inner ear Inferred relationship Some
Neutropenia-monocytopenia-deafness syndrome is characterized by neutropenia with myeloid marrow hypoplasia, monocytopenia, and congenital deafness. It has been described in three siblings who suffered recurrent bacterial infections. Is a True Congenital anomaly of inner ear Inferred relationship Some
Sinoatrial node dysfunction and deafness is a rare genetic disease characterized by congenital severe to profound deafness with no evidence of vestibular dysfunction, associated with sinoatrial node dysfunction with pronounced bradycardia and increased variability of heart rate at rest and episodic syncopes that may be triggered by enhanced physical activity and stress. Is a True Congenital anomaly of inner ear Inferred relationship Some
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. Is a True Congenital anomaly of inner ear Inferred relationship Some

This concept is not in any reference sets

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