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Standards Ontologies Notations
Guidelines
MIRAGE
sensorineural hearing loss

Summary
Synonym
  • High Frequency Hearing Loss
  • High frequency deafness
  • Perceptive deafness
  • Perceptive hearing loss
  • Perceptive hearing loss or deafness
  • Sensorineural Deafness
  • Sensory hearing loss
  • central hearing loss
  • high-frequency hearing loss
Definition
An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem.
Super Class
inner ear disease
Disease Ontology
DOID:10003
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 11 - 20 of 24 in total
Gene ID Gene Symbol Description Source
3673 ITGA2 integrin subunit alpha 2
4153 MBL2 mannose binding lectin 2
4627 MYH9 myosin heavy chain 9
4640 MYO1A myosin IA
4646 MYO6 myosin VI
4647 MYO7A myosin VIIA
7007 TECTA tectorin alpha
7124 TNF tumor necrosis factor
7466 WFS1 wolframin ER transmembrane glycoprotein
25861 WHRN whirlin
Displaying 1 entry
Gene ID Gene Symbol Description Source
241919 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14
Displaying 1 entry
Gene ID Gene Symbol Description Source
50672 Ednrb endothelin receptor type B
Displaying all 2 entries
Gene ID Gene Symbol Description Source
34615 Rh5 Rhodopsin 5
41889 Rh6 Rhodopsin 6
Displaying 1 entry
Gene ID Gene Symbol Description Source
393385 slc44a4 solute carrier family 44 member 4
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q8BXR1 Solute carrier family 7 member 14
Displaying 1 entry
UniProt ID Protein Name Source
P21451 Endothelin receptor type B
Displaying all 2 entries
UniProt ID Protein Name Source
O01668 Opsin Rh6
P91657 Opsin Rh5
Displaying 1 entry
UniProt ID Protein Name Source
Q7T2B0 Choline transporter-like protein 4
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025