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autosomal recessive nonsyndromic hearing loss 65 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 65

MONDO:0012452

Also known as:DFNB65autosomal recessive deafness 65autosomal recessive nonsyndromic deafness 65

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 20q13.2-q13.3.

GeneticsAutosomal recessive

ResearchLimited published research (9 articles)

Clinical Presentation

Features include: Hearing loss (hearing impairment).

Organ System	Phenotype Count	Example Features
Ears	1	Hearing loss (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 65.

9 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 65. Research spans Basic Science / Preclinical (56%), Review / Meta-Analysis (11%), and Case Report / Case Series (11%).

Recent Publications

Pshennikova VG (2026). [PMID: 40957967](https://pubmed.ncbi.nlm.nih.gov/40957967/). *J Hum Genet*. [Basic Science / Preclinical]
Huynh BC (2026). [PMID: 41845931](https://pubmed.ncbi.nlm.nih.gov/41845931/). *Ophthalmic Genet*. [Basic Science / Preclinical]
Peng LT (2026). [PMID: 41351289](https://pubmed.ncbi.nlm.nih.gov/41351289/). *J Clin Lab Anal*. [Basic Science / Preclinical]
Riahi Z (2025). [PMID: 41359850](https://pubmed.ncbi.nlm.nih.gov/41359850/). *Proc Natl Acad Sci U S A*. [Basic Science / Preclinical]
Liu Y (2025). [PMID: 40555484](https://pubmed.ncbi.nlm.nih.gov/40555484/). *Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi*. [Clinical Trial Publication]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 4:33 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:610248

GARD

Genetic and Rare Diseases Info Center

GARD:22623

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 65

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