autosomal recessive nonsyndromic deafness 39

Summary
Synonym
  • DFNB39
  • autosomal recessive deafness 39
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21.
Super Class
autosomal recessive nonsyndromic deafness
Disease Ontology
DOID:0110497
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3082 HGF hepatocyte growth factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
15234 Hgf hepatocyte growth factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
24446 Hgf hepatocyte growth factor

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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