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autosomal recessive nonsyndromic hearing loss 85 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 85

MONDO:0013250

Also known as:DFNB85autosomal recessive deafness 85autosomal recessive nonsyndromic deafness 85

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 17p12-q11.2.

GeneticsAutosomal recessive

OnsetCONGENITAL

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

Age of onset: at birth.

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 85.

4 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 85. Research spans Basic Science / Preclinical (50%), Clinical Trial Publication (25%), and Gene Therapy / Novel Therapeutics (25%).

Recent Publications

Zhang L (2025). [PMID: 40409265](https://pubmed.ncbi.nlm.nih.gov/40409265/). *Med*. [Gene Therapy / Novel Therapeutics]
Liao B (2025). [PMID: 39777619](https://pubmed.ncbi.nlm.nih.gov/39777619/). *Genes Genomics*. [Basic Science / Preclinical]
Zaw K (2025). [PMID: 40184886](https://pubmed.ncbi.nlm.nih.gov/40184886/). *Stem Cell Res*. [Basic Science / Preclinical]
Wang H (2024). [PMID: 38839897](https://pubmed.ncbi.nlm.nih.gov/38839897/). *Nat Med*. [Clinical Trial Publication]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 6:58 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:613392

GARD

Genetic and Rare Diseases Info Center

GARD:22635

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 85

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