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An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 2p12.
Features include: Inner ear hearing loss (sensorineural hearing impairment) and Tinnitus.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Ears | 2 | Inner ear hearing loss (sensorineural hearing impairment), Tinnitus |
No clinical trials have been registered for autosomal dominant nonsyndromic hearing loss 43.
3 publications have been identified in PubMed for autosomal dominant nonsyndromic hearing loss 43. Research spans Case Report / Case Series (67%) and Basic Science / Preclinical (33%).
Peng LT (2026). [PMID: 41351289](https://pubmed.ncbi.nlm.nih.gov/41351289/). *J Clin Lab Anal*. [Case Report / Case Series]
Simmons JH (2025). [PMID: 40222603](https://pubmed.ncbi.nlm.nih.gov/40222603/). *Bone*. [Case Report / Case Series]
Reichenberger EJ (2024). [PMID: 39165910](https://pubmed.ncbi.nlm.nih.gov/39165910/). *JBMR Plus*. [Basic Science / Preclinical]
Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 3:23 AM UTC
Online Mendelian Inheritance in Man
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