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autosomal recessive nonsyndromic hearing loss 83 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 83

MONDO:0013365

Also known as:DFNB83autosomal recessive deafness 83autosomal recessive nonsyndromic deafness 83

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 9p23-p21.2.

GeneticsAutosomal recessive

ResearchLimited published research (4 articles)

Clinical Presentation

Features include: Prelingual sensorineural hearing impairment.

Organ System	Phenotype Count	Example Features
Ears	1	Prelingual sensorineural hearing impairment

Explore clinical features

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 83.

4 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 83. Research spans Basic Science / Preclinical (50%) and Epidemiology / Natural History (50%).

Recent Publications

Zaman Q (2025). [PMID: 40404069](https://pubmed.ncbi.nlm.nih.gov/40404069/). *Gene*. [Basic Science / Preclinical]
Yang Y (2025). [PMID: 40583560](https://pubmed.ncbi.nlm.nih.gov/40583560/). *Hum Mol Genet*. [Basic Science / Preclinical]
Rodriguez-Valero M (2024). [PMID: 38855775](https://pubmed.ncbi.nlm.nih.gov/38855775/). *Laryngoscope Investig Otolaryngol*. [Epidemiology / Natural History]
Antunes LN (2024). [PMID: 39498320](https://pubmed.ncbi.nlm.nih.gov/39498320/). *Front Genet*. [Epidemiology / Natural History]

Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 9:15 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:613685

GARD

Genetic and Rare Diseases Info Center

GARD:22637

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 83

Overview

Clinical Presentation

Explore clinical features

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team