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autosomal recessive nonsyndromic hearing loss 13 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 13

MONDO:0011286

Also known as:DFNB13autosomal recessive deafness 13autosomal recessive nonsyndromic deafness 13

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 7q34-q36.

GeneticsAutosomal recessive

Clinical Presentation

Built from Human Phenotype Ontology (HPO) phenotype annotations and GeneReviews clinical descriptions. Features represent findings documented across known cases — not an exhaustive list of possible symptoms.

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

Organ System	Phenotype Count	Example Features
Ears	2	Hearing loss (hearing impairment), Inner ear hearing loss (sensorineural hearing impairment)

Explore clinical features

Diagnosis

Biomarker and diagnostic research for autosomal recessive nonsyndromic hearing loss 13 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 13.

29 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 13. Research spans Case Report / Case Series (38%), Epidemiology / Natural History (24%), and Basic Science / Preclinical (17%).

Research Type	Count	% of Total
Patient case studies	11	38%

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 6:03 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:603098

GARD

Genetic and Rare Diseases Info Center

GARD:22594

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 13

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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