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autosomal dominant nonsyndromic hearing loss 18 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant nonsyndromic hearing loss 18

MONDO:0011625

Also known as:DFNA18autosomal dominant deafness 18autosomal dominant nonsyndromic deafness 18

Overview

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 3q22.

GeneticsAutosomal dominant

Clinical Presentation

Features include: Progressive hearing impairment.

Organ System	Phenotype Count	Example Features
Ears	1	Progressive 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 18.

15 publications have been identified in PubMed for autosomal dominant nonsyndromic hearing loss 18. Research spans Case Report / Case Series (57%), Review / Meta-Analysis (14%), and Epidemiology / Natural History (14%).

Research Type	Count	% of Total
Patient case studies	8	57%

Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 9:43 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:606012

GARD

Genetic and Rare Diseases Info Center

GARD:18113

Questions for Your Care Team

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autosomal dominant nonsyndromic hearing loss 18

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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