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autosomal recessive nonsyndromic hearing loss 14 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 14

MONDO:0011360

Also known as:DFNB14autosomal recessive deafness 14autosomal recessive nonsyndromic deafness 14

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation between D7S554 and D7S2459 in the chromosome region 7q31.

GeneticsAutosomal recessive

OnsetINFANTILE

Clinical Presentation

Features include: Inner ear hearing loss (sensorineural hearing impairment).

Organ System	Phenotype Count	Example Features
Ears	1	Inner ear hearing loss (sensorineural hearing impairment)

Age of onset: infancy.

Explore clinical features

Diagnosis

Biomarker and diagnostic research for autosomal recessive nonsyndromic hearing loss 14 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 14.

21 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 14. Research spans Case Report / Case Series (33%), Epidemiology / Natural History (19%), and Clinical Trial Publication (14%).

Research Type	Count	% of Total
Patient case studies	7	33%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 12:50 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:603678

GARD

Genetic and Rare Diseases Info Center

GARD:22596

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 14

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

GARD

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Questions for Your Care Team

Questions for Your Care Team

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