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autosomal dominant nonsyndromic hearing loss 16 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant nonsyndromic hearing loss 16

MONDO:0011389

Also known as:DFNA16autosomal dominant deafness 16autosomal dominant nonsyndromic deafness 16

Overview

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 2q23-q24.3.

GeneticsAutosomal dominant

Clinical Presentation

Features include sometimes findings: Tinnitus. 2 total HPO annotations.

Organ System	Phenotype Count	Example Features
Ears	2	Tinnitus, Adult onset sensorineural hearing impairment

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Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for autosomal dominant nonsyndromic hearing loss 16.

18 publications have been identified in PubMed for autosomal dominant nonsyndromic hearing loss 16. Research spans Case Report / Case Series (33%), Basic Science / Preclinical (33%), and Epidemiology / Natural History (17%).

Research Type	Count	% of Total
Patient case studies	6	33%

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 12:32 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:603964

GARD

Genetic and Rare Diseases Info Center

GARD:18110

Questions for Your Care Team

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autosomal dominant nonsyndromic hearing loss 16

Overview

Clinical Presentation

Explore clinical features

Research Landscape

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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