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autosomal dominant nonsyndromic hearing loss 31 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant nonsyndromic hearing loss 31

MONDO:0012086

Also known as:DFNA31autosomal dominant deafness 31autosomal dominant nonsyndromic deafness 31

Overview

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 6p21.3.

GeneticsAutosomal dominant

Clinical Presentation

Features include: Old-aged sensorineural hearing impairment.

Organ System	Phenotype Count	Example Features
Ears	1	Old-aged sensorineural hearing impairment

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Diagnosis

Biomarker and diagnostic research for autosomal dominant nonsyndromic hearing loss 31 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 31.

11 publications have been identified in PubMed for autosomal dominant nonsyndromic hearing loss 31. Research spans Case Report / Case Series (45%), Diagnostic / Biomarker (18%), and Epidemiology / Natural History (18%).

Research Type	Count	% of Total
Patient case studies	5	45%

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 8:42 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:608645

GARD

Genetic and Rare Diseases Info Center

GARD:18125

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autosomal dominant nonsyndromic hearing loss 31

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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