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autosomal recessive nonsyndromic hearing loss 51 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 51

MONDO:0012370

Also known as:DFNB51autosomal recessive deafness 51autosomal recessive nonsyndromic deafness 51

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 11p13-p12.

GeneticsAutosomal recessive

OnsetINFANTILE

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)

Age of onset: infancy.

Explore clinical features

Diagnosis

Biomarker and diagnostic research for autosomal recessive nonsyndromic hearing loss 51 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 recessive nonsyndromic hearing loss 51.

10 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 51. Research spans Review / Meta-Analysis (30%), Case Report / Case Series (30%), and Epidemiology / Natural History (20%).

Research Type	Count	% of Total
Research summaries	3	30%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 9:43 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:609941

GARD

Genetic and Rare Diseases Info Center

GARD:9918

Questions for Your Care Team

→Should my partner and I meet with a genetic counselor to discuss carrier status and family planning?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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autosomal recessive nonsyndromic hearing loss 51

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

GARD

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Questions for Your Care Team

Questions for Your Care Team

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