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autosomal recessive nonsyndromic hearing loss 15

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The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Disease Overview

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GIPC3 gene.

Synonyms

  • DFNB15
  • DFNB72
  • DFNB95
  • GIPC3 autosomal recessive nonsyndromic deafness
  • autosomal recessive deafness 15
  • autosomal recessive deafness 72
  • autosomal recessive deafness 95
  • autosomal recessive nonsyndromic deafness 15
  • autosomal recessive nonsyndromic deafness caused by mutation in GIPC3
  • autosomal recessive nonsyndromic deafness type 15
  • autosomal recessive nonsyndromic hearing loss 15
  • deafness, autosomal recessive 15
  • deafness, autosomal recessive 72
  • deafness, autosomal recessive 95
  • deafness, autosomal recessive type 15
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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