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autosomal dominant nonsyndromic hearing loss 59 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal dominant nonsyndromic hearing loss 59

MONDO:0012974

Also known as:DFNA59autosomal dominant deafness 59autosomal dominant nonsyndromic deafness 59

Overview

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 11p14.2-q12.3.

GeneticsAutosomal dominant

OnsetCONGENITAL

ResearchLimited published research (1 article)

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 always present findings: 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: at birth.

Explore clinical features

Diagnosis

Biomarker and diagnostic research for autosomal dominant nonsyndromic hearing loss 59 has been reported in the published literature.

Prognosis

Phenotype severity distribution: 1 always present feature.

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 dominant nonsyndromic hearing loss 59.

1 publication has been identified in PubMed for autosomal dominant nonsyndromic hearing loss 59. Research spans Diagnostic / Biomarker (100%).

Recent Publications

Kim JA (2025). [PMID: 40164689](https://pubmed.ncbi.nlm.nih.gov/40164689/). *Experimental & molecular medicine*. [Diagnostic / Biomarker]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 8:02 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:612642

GARD

Genetic and Rare Diseases Info Center

GARD:18129

Questions for Your Care Team

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autosomal dominant nonsyndromic hearing loss 59

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team