Sensorineural Hearing Loss

Alias:
Sensory Hearing Loss
Hearing Loss, Sensorineural
Perceptive Hearing Loss or Deafness
Sensorineural Hearing Loss Disorder
Hearing Loss, High-Frequency
High Frequency Hearing Loss
High-Frequency Hearing Loss
Hearing Loss High-Frequency
Hearing Loss Sensorineural
High Frequency Deafness
Perceptive Hearing Loss
Sensorineural Deafness
Deafness Sensorineural
Hearing Loss, Central
Central Hearing Loss
Perceptive Deafness
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Sensorineural Hearing Loss, also known as sensory hearing loss, is related to deafness, autosomal dominant 1, with or without thrombocytopenia and rare autosomal recessive non-syndromic sensorineural deafness type dfnb, and has symptoms including tinnitus An important gene associated with Sensorineural Hearing Loss is GJB2 (Gap Junction Protein Beta 2), and among its related pathways/superpathways are Sensory processing of sound and Aminoglycoside Ototoxicity Pathway, Adverse Drug Reaction. The drugs Prednisolone and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include bone and bone marrow, and related phenotypes are nervous system and hearing/vestibular/ear
Related ID:
MESH:D006319

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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276
2517
4

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
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Gene & Mutation

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Disease Model

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MGI
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References Literature

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