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autosomal recessive nonsyndromic hearing loss 96 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 96

MONDO:0013738

Also known as:DFNB96autosomal recessive deafness 96autosomal recessive nonsyndromic deafness 96

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 1p36.31-p36.13.

GeneticsAutosomal recessive

ResearchLimited published research (7 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 96.

7 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 96. Research spans Clinical Trial Publication (29%), Basic Science / Preclinical (29%), and Review / Meta-Analysis (14%).

Recent Publications

Abati E (2026). [PMID: 42089726](https://pubmed.ncbi.nlm.nih.gov/42089726/). *J Neuromuscul Dis*. [Review / Meta-Analysis]
Jiang L (2026). [PMID: 42020731](https://pubmed.ncbi.nlm.nih.gov/42020731/). *Nature*. [Gene Therapy / Novel Therapeutics]
Wu L (2026). [PMID: 41895920](https://pubmed.ncbi.nlm.nih.gov/41895920/). *J Mol Diagn*. [Clinical Trial Publication]
Colbert BM (2025). [PMID: 39560289](https://pubmed.ncbi.nlm.nih.gov/39560289/). *Laryngoscope*. [Basic Science / Preclinical]
Zhang T (2025). [PMID: 40364746](https://pubmed.ncbi.nlm.nih.gov/40364746/). *Mol Genet Genomic Med*. [Case Report / Case Series]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 11:57 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:614414

GARD

Genetic and Rare Diseases Info Center

GARD:22642

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 96

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