autosomal dominant nonsyndromic hearing loss 23

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Disease Overview

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the SIX1 gene.

Synonyms

DFNA 23
DFNA23
SIX1 autosomal dominant nonsyndromic deafness
autosomal dominant deafness 23
autosomal dominant nonsyndromic deafness 23
autosomal dominant nonsyndromic deafness caused by mutation in SIX1
autosomal dominant nonsyndromic deafness type 23
deafness, autosomal dominant 23
deafness, autosomal dominant nonsyndromic sensorineural 23
deafness, autosomal dominant type 23

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.