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autosomal dominant nonsyndromic hearing loss 33 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant nonsyndromic hearing loss 33

MONDO:0013632

Also known as:DFNA33autosomal dominant deafness 33autosomal dominant nonsyndromic deafness 33

Overview

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 13q34.

GeneticsAutosomal dominant

ResearchLimited published research (8 articles)

Clinical Presentation

Features include: Inner ear hearing loss (sensorineural hearing impairment) and Tinnitus.

Organ System	Phenotype Count	Example Features
Ears	2	Inner ear hearing loss (sensorineural hearing impairment), Tinnitus

Explore clinical features

Diagnosis

Biomarker and diagnostic research for autosomal dominant nonsyndromic hearing loss 33 has been reported in the published literature.

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 33.

8 publications have been identified in PubMed for autosomal dominant nonsyndromic hearing loss 33. Research spans Review / Meta-Analysis (38%), Case Report / Case Series (25%), and Epidemiology / Natural History (25%).

Recent Publications

Hoang NC (2026). [PMID: 41955303](https://pubmed.ncbi.nlm.nih.gov/41955303/). *Human molecular genetics*. [Epidemiology / Natural History]
Peng LT (2026). [PMID: 41351289](https://pubmed.ncbi.nlm.nih.gov/41351289/). *Journal of clinical laboratory analysis*. [Case Report / Case Series]
Leduc F (2025). [PMID: 40348827](https://pubmed.ncbi.nlm.nih.gov/40348827/). *European journal of human genetics : EJHG*. [Review / Meta-Analysis]
Kim JA (2025). [PMID: 40164689](https://pubmed.ncbi.nlm.nih.gov/40164689/). *Experimental & molecular medicine*. [Epidemiology / Natural History]
Gong GQ (2025). [PMID: 40052770](https://pubmed.ncbi.nlm.nih.gov/40052770/). *Molecular genetics & genomic medicine*. [Case Report / Case Series]

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 5:50 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:614211

GARD

Genetic and Rare Diseases Info Center

GARD:18135

Questions for Your Care Team

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autosomal dominant nonsyndromic hearing loss 33

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team