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autosomal dominant nonsyndromic hearing loss 47 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant nonsyndromic hearing loss 47

MONDO:0012090

Also known as:DFNA47autosomal dominant deafness 47autosomal dominant nonsyndromic deafness 47

Overview

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 9p22-p21.

GeneticsAutosomal dominant

ResearchLimited published research (8 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 47 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 47.

8 publications have been identified in PubMed for autosomal dominant nonsyndromic hearing loss 47. Research spans Review / Meta-Analysis (25%), Case Report / Case Series (25%), and Diagnostic / Biomarker (13%).

Recent Publications

Kim JA (2025). [PMID: 40164689](https://pubmed.ncbi.nlm.nih.gov/40164689/). *Exp Mol Med*. [Review / Meta-Analysis]
Guan J (2025). [PMID: 40068948](https://pubmed.ncbi.nlm.nih.gov/40068948/). *Yi Chuan*. [Diagnostic / Biomarker]
Gong GQ (2025). [PMID: 40052770](https://pubmed.ncbi.nlm.nih.gov/40052770/). *Mol Genet Genomic Med*. [Case Report / Case Series]
Al-Bustanji R (2025). [PMID: 41305774](https://pubmed.ncbi.nlm.nih.gov/41305774/). *Medicine (Baltimore)*. [Case Report / Case Series]
Yuan YY (2025). [PMID: 40010783](https://pubmed.ncbi.nlm.nih.gov/40010783/). *Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi*. [Clinical Trial Publication]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 10:00 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:608652

GARD

Genetic and Rare Diseases Info Center

GARD:18126

Questions for Your Care Team

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autosomal dominant nonsyndromic hearing loss 47

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