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autosomal recessive nonsyndromic hearing loss 24 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 24

MONDO:0012602

Also known as:DFNB24RDX autosomal recessive nonsyndromic deafnessautosomal recessive deafness 24

Overview

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the RDX gene.

GeneticsAutosomal recessive · RDX (chr 11)

Clinical Presentation

Features include: Profound sensorineural hearing impairment.

Organ System	Phenotype Count	Example Features
Ears	1	Profound sensorineural hearing impairment

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Genetic Landscape

RDX function has not been fully characterized.

Autosomal recessive nonsyndromic hearing loss 24 is associated with mutations in the RDX gene on chromosome 11.

Diagnosis

Drawn from GeneReviews diagnostic guidelines, newborn screening panel status (RUSP), and ClinGen gene-disease validity classifications. Reflects current clinical evidence and consensus where available.

Genetic testing for RDX is available. Testing is considered confirmatory for diagnosis.

Biomarker and diagnostic research for autosomal recessive nonsyndromic hearing loss 24 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 24.

15 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 24. Research spans Case Report / Case Series (27%), Diagnostic / Biomarker (20%), and Epidemiology / Natural History (20%).

Research Type	Count	% of Total
Patient case studies	4	27%

Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 2:57 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:611022

GARD

Genetic and Rare Diseases Info Center

GARD:22626

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 24

Overview

Clinical Presentation

Explore clinical features

Genetic Landscape

Diagnosis

Research Landscape

Medical References

External Resources

OMIM

GARD

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Questions for Your Care Team

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