autosomal dominant nonsyndromic hearing loss 12

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Disease Overview

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

Synonyms

DFNA12
DFNA8
TECTA autosomal dominant nonsyndromic deafness
autosomal dominant deafness 12
autosomal dominant deafness 8
autosomal dominant nonsyndromic deafness 12
autosomal dominant nonsyndromic deafness caused by mutation in TECTA
autosomal dominant nonsyndromic deafness type 12
autosomal dominant nonsyndromic hearing loss 12
deafness, autosomal dominant 12
deafness, autosomal dominant 8
deafness, autosomal dominant 8/12
deafness, autosomal dominant type 12

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.