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autosomal recessive nonsyndromic hearing loss 62 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 62

MONDO:0012418

Also known as:DFNB62autosomal recessive deafness 62autosomal recessive nonsyndromic deafness 62

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 12p13.2-p11.23.

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

Diagnosis

Biomarker and diagnostic research for autosomal recessive nonsyndromic hearing loss 62 has been reported in the published literature.

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 62.

6 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 62. Research spans Case Report / Case Series (67%), Diagnostic / Biomarker (17%), and Epidemiology / Natural History (17%).

Recent Publications

Gan H (2026). [PMID: 41578500](https://pubmed.ncbi.nlm.nih.gov/41578500/). *Medicine (Baltimore)*. [Case Report / Case Series]
Ding Y (2025). [PMID: 40195191](https://pubmed.ncbi.nlm.nih.gov/40195191/). *Eur Arch Otorhinolaryngol*. [Diagnostic / Biomarker]
Yadav B (2024). [PMID: 40654386](https://pubmed.ncbi.nlm.nih.gov/40654386/). *JNMA J Nepal Med Assoc*. [Case Report / Case Series]
Whyte MP (2024). [PMID: 39084544](https://pubmed.ncbi.nlm.nih.gov/39084544/). *Bone*. [Case Report / Case Series]
AitRaise I (2024). [PMID: 37777971](https://pubmed.ncbi.nlm.nih.gov/37777971/). *Biochem Genet*. [Case Report / Case Series]

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 5:51 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:610143

GARD

Genetic and Rare Diseases Info Center

GARD:22618

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 62

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team