autosomal recessive nonsyndromic deafness 61

Summary
Synonym
  • DFNB61
  • autosomal recessive deafness 61
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the SLC26A5 gene on chromosome 7q22.
Super Class
autosomal recessive nonsyndromic deafness
Disease Ontology
DOID:0110513
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
375611 SLC26A5 solute carrier family 26 member 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
80979 Slc26a5 solute carrier family 26, member 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
83819 Slc26a5 solute carrier family 26 member 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
322846 slc26a5 solute carrier family 26 member 5

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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: December 9, 2024