autosomal dominant nonsyndromic deafness 88

Summary
Synonym
  • DFNA88
  • autosomal dominant deafness 88
Definition
An autosomal dominant nonsyndromic deafness characterized by postlingual progressive severe sensorineural hearing loss with tinnitus that has_material_basis_in heterozygous mutation in the EPHA10 gene on chromosome 1p34.
Super Class
autosomal dominant nonsyndromic deafness
Disease Ontology
DOID:0070611
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
284656 EPHA10 EPH receptor A10
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q5JZY3 Ephrin type-A receptor 10

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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