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autosomal recessive nonsyndromic hearing loss 20 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive nonsyndromic hearing loss 20

MONDO:0011392

Also known as:DFNB20autosomal recessive deafness 20autosomal recessive nonsyndromic deafness 20

Overview

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 11q25-qter.

GeneticsAutosomal recessive

OnsetINFANTILE

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)

Age of onset: infancy.

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 20.

23 publications have been identified in PubMed for autosomal recessive nonsyndromic hearing loss 20. Research spans Case Report / Case Series (43%), Basic Science / Preclinical (22%), and Epidemiology / Natural History (17%).

Research Type	Count	% of Total
Patient case studies	10	43%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 9:42 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:604060

GARD

Genetic and Rare Diseases Info Center

GARD:22598

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 20

Overview

Clinical Presentation

Explore clinical features

Research Landscape

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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