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

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant auditory neuropathy 1 itself.

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↑ Auditory neuropathy (11) ↑ Autosomal dominant nonsyndromic hearing loss (2)

Including sub-types (0) Tagged with Autosomal dominant auditory neuropathy 1 (0)

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