nonsyndromic deafness

Summary
Synonym
  • nonsyndromic hearing loss
  • nonsyndromic hereditary hearing loss
Definition
An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms.
Super Class
auditory system disease
Disease Ontology
DOID:0050563
Mondo Disease Ontology
MeSH
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7399 USH2A usherin
Displaying all 2 entries
Gene ID Gene Symbol Description Source
22393 Wfs1 wolframin ER transmembrane glycoprotein
380959 Alg10b ALG10 alpha-1,2-glucosyltransferase
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
O75445 Usherin
Displaying 1 entry
UniProt ID Protein Name Source
Q80UI9 Wolfram syndrome 1 homolog (Human)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: April 7, 2025