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autosomal dominant nonsyndromic hearing loss 65

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Disease Overview

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the TBC1D24 gene.

Synonyms

  • DFNA65
  • TBC1D24 autosomal dominant nonsyndromic deafness
  • autosomal dominant deafness 65
  • autosomal dominant nonsyndromic deafness 65
  • autosomal dominant nonsyndromic deafness caused by mutation in TBC1D24
  • autosomal dominant nonsyndromic deafness type 65
  • deafness, autosomal dominant 65
  • deafness, autosomal dominant type 65
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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GeneReviews

GeneReviews has an article on this condition covering diagnosis, management, and inheritance. Each article is written by one or more experts on the specific disease and is reviewed by other specialists. The article contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. The GeneReviews database is managed by the University of Washington.

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