autosomal dominant nonsyndromic deafness 69

Summary
Synonym
  • DCUA
  • DFNA69
  • autosomal dominant deafness 69
  • unilateral or asymmetric congenital deafness
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21.
Super Class
autosomal dominant nonsyndromic deafness
Disease Ontology
DOID:0110590
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4254 KITLG KIT ligand
Displaying 1 entry
Gene ID Gene Symbol Description Source
17311 Kitl kit ligand
Displaying 1 entry
Gene ID Gene Symbol Description Source
60427 Kitlg KIT ligand

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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