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autosomal dominant nonsyndromic hearing loss 30 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant nonsyndromic hearing loss 30

MONDO:0011673

Also known as:DFNA30autosomal dominant deafness 30autosomal dominant nonsyndromic deafness 30

Overview

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 15q25-q26.

GeneticsAutosomal dominant

ResearchLimited published research (9 articles)

Clinical Presentation

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

Organ System	Phenotype Count	Example Features
Ears	1	Inner ear hearing loss (sensorineural hearing impairment)

Explore clinical features

Diagnosis

Biomarker and diagnostic research for autosomal dominant nonsyndromic hearing loss 30 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 30.

10 publications have been identified in PubMed for autosomal dominant nonsyndromic hearing loss 30. Research spans Case Report / Case Series (78%), Diagnostic / Biomarker (11%), and Basic Science / Preclinical (11%).

Recent Publications

Peng LT (2026). [PMID: 41351289](https://pubmed.ncbi.nlm.nih.gov/41351289/). *J Clin Lab Anal*. [Case Report / Case Series]
Rietmann SJ (2026). [PMID: 41601192](https://pubmed.ncbi.nlm.nih.gov/41601192/). *Anim Genet*. [Case Report / Case Series]
DeSollar B (2026). [PMID: 41979979](https://pubmed.ncbi.nlm.nih.gov/41979979/). *JMIR Bioinform Biotechnol*. [Diagnostic / Biomarker]
Yang C (2026). [PMID: 41822198](https://pubmed.ncbi.nlm.nih.gov/41822198/). *Exp Ther Med*. [Case Report / Case Series]
Guan J (2025). [PMID: 40068948](https://pubmed.ncbi.nlm.nih.gov/40068948/). *Yi Chuan*. [Basic Science / Preclinical]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 9:41 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:606451

GARD

Genetic and Rare Diseases Info Center

GARD:18114

Questions for Your Care Team

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autosomal dominant nonsyndromic hearing loss 30

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