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autosomal recessive nonsyndromic hearing loss 61 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 61

MONDO:0013471

Also known as:DFNB61SLC26A5 autosomal recessive nonsyndromic deafnessautosomal recessive deafness 61

Overview

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SLC26A5 gene.

GeneticsAutosomal recessive · SLC26A5 (chr 7)

OnsetCONGENITAL

ResearchLimited published research (2 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)

Age of onset: at birth.

Explore clinical features

Genetic Landscape

SLC26A5 function has not been fully characterized.

Autosomal recessive nonsyndromic hearing loss 61 is associated with mutations in the SLC26A5 gene on chromosome 7.

Diagnosis

Genetic testing for SLC26A5 is available. Testing is considered confirmatory for diagnosis.

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 61.

2 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 61. Research spans Review / Meta-Analysis (50%) and Basic Science / Preclinical (50%).

Recent Publications

Abati E (2026). [PMID: 42089726](https://pubmed.ncbi.nlm.nih.gov/42089726/). *J Neuromuscul Dis*. [Review / Meta-Analysis]
Yalcouyé A (2025). [PMID: 39663698](https://pubmed.ncbi.nlm.nih.gov/39663698/). *HGG Adv*. [Basic Science / Preclinical]

Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 9:42 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:613865

GARD

Genetic and Rare Diseases Info Center

GARD:22639

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 61

Overview

Clinical Presentation

Explore clinical features

Genetic Landscape

Diagnosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

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Questions for Your Care Team

Questions for Your Care Team