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autosomal recessive nonsyndromic hearing loss 71 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 71

MONDO:0013010

Also known as:DFNB71autosomal recessive deafness 71autosomal recessive nonsyndromic deafness 71

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 8p22-p21.3.

GeneticsAutosomal recessive

ResearchLimited published research (6 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 71.

6 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 71. Research spans Basic Science / Preclinical (33%), Epidemiology / Natural History (33%), and Review / Meta-Analysis (17%).

Recent Publications

Pshennikova VG (2026). [PMID: 40957967](https://pubmed.ncbi.nlm.nih.gov/40957967/). *J Hum Genet*. [Basic Science / Preclinical]
Kutija Fučkar I (2026). [PMID: 42074586](https://pubmed.ncbi.nlm.nih.gov/42074586/). *Genes (Basel)*. [Epidemiology / Natural History]
Kim JA (2025). [PMID: 40164689](https://pubmed.ncbi.nlm.nih.gov/40164689/). *Exp Mol Med*. [Review / Meta-Analysis]
Long X (2025). [PMID: 40410890](https://pubmed.ncbi.nlm.nih.gov/40410890/). *Hum Genomics*. [Basic Science / Preclinical]
Rodriguez-Valero M (2024). [PMID: 38855775](https://pubmed.ncbi.nlm.nih.gov/38855775/). *Laryngoscope Investig Otolaryngol*. [Epidemiology / Natural History]

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 12:29 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:612789

GARD

Genetic and Rare Diseases Info Center

GARD:22630

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 71

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