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Autosomal dominant auditory neuropathy 1

MONDO:0012196

Any auditory neuropathy in which the cause of the disease is a mutation in the DIAPH3 gene.

Also known as: AUNA1, DIAPH3 auditory neuropathy, NSDAN, auditory neuropathy caused by mutation in DIAPH3, auditory neuropathy, autosomal dominant, type 1, autosomal dominant auditory neuropathy type 1, auditory neuropathy, autosomal dominant, 1, auditory neuropathy, nonsyndromic dominant

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) Auditory neuropathy (6) Hereditary neurological disease (5) Nonsyndromic genetic hearing loss (3)
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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