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autosomal recessive nonsyndromic hearing loss 76

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Disease Overview

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SYNE4 gene.

Synonyms

  • DFNB76
  • SYNE4 autosomal recessive nonsyndromic deafness
  • autosomal recessive deafness 76
  • autosomal recessive nonsyndromic deafness 76
  • autosomal recessive nonsyndromic deafness caused by mutation in SYNE4
  • autosomal recessive nonsyndromic deafness type 76
  • autosomal recessive nonsyndromic hearing loss 76
  • deafness, autosomal recessive 76
  • deafness, autosomal recessive type 76
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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