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autosomal dominant nonsyndromic hearing loss 24 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant nonsyndromic hearing loss 24

MONDO:0011657

Also known as:DFNA 24DFNA24autosomal dominant deafness 24

Overview

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 4q35-qter.

GeneticsAutosomal dominant

ResearchLimited published research (5 articles)

Clinical Presentation

Features include: Hearing loss (hearing impairment).

Organ System	Phenotype Count	Example Features
Ears	1	Hearing loss (hearing impairment)

Explore clinical features

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 24.

7 publications have been identified in PubMed for autosomal dominant nonsyndromic hearing loss 24. Kisho has analyzed 5 by research type. Research spans Case Report / Case Series (40%), Review / Meta-Analysis (20%), and Basic Science / Preclinical (20%).

Recent Publications

Peng LT (2026). [PMID: 41351289](https://pubmed.ncbi.nlm.nih.gov/41351289/). *J Clin Lab Anal*. [Basic Science / Preclinical]
Mumm S (2025). [PMID: 40204055](https://pubmed.ncbi.nlm.nih.gov/40204055/). *Bone*. [Case Report / Case Series]
Gong GQ (2025). [PMID: 40052770](https://pubmed.ncbi.nlm.nih.gov/40052770/). *Mol Genet Genomic Med*. [Case Report / Case Series]
Antunes LN (2024). [PMID: 39498320](https://pubmed.ncbi.nlm.nih.gov/39498320/). *Front Genet*. [Epidemiology / Natural History]
Giuca MR (2024). [PMID: 39212455](https://pubmed.ncbi.nlm.nih.gov/39212455/). *Eur J Paediatr Dent*. [Review / Meta-Analysis]

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 5:51 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:606282

GARD

Genetic and Rare Diseases Info Center

GARD:9166

Questions for Your Care Team

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autosomal dominant nonsyndromic hearing loss 24

Overview

Clinical Presentation

Explore clinical features

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team