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Autosomal dominant nonsyndromic hearing loss 27

MONDO:0012902

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 4q12-q13.1.

Also known as: DFNA27, autosomal dominant deafness 27, autosomal dominant nonsyndromic deafness 27, autosomal dominant nonsyndromic deafness type 27, deafness, autosomal dominant 27

60 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hearing loss disorder (254) Nervous system disorder (217) Hereditary disease (172) Perceptual disorders (21) Hearing disorder (19) Human disease (14) Hereditary neurological disease (5) Nonsyndromic genetic hearing loss (3) Disease of genetic or genomic mechanism (2)
Trials to join now! 21 Not yet recruiting 13 Not yet finished but already full! 8 Completed 17 Terminated 1
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  • Cochlear implant study tests new sound processor for better hearing

    Knowledge-focused Terminated

    This study tested how well adults with a NeuroZti cochlear implant could hear and how satisfied they were with two different sound processors: the current Neu2 and a newer Nuc8. Four participants attended a single 3-hour visit to compare speech understanding at normal and soft vo…

    Phase: NA • Sponsor: Cochlear • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:36 UTC

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