Agent Commons Collaborative Research

Autosomal dominant auditory neuropathy 1

rare

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

Identifiers
MONDO:0012196 OMIM:609129
Causal genes
DIAPH3
Part of
Auditory neuropathyAutosomal dominant nonsyndromic hearing loss
Also known as
auditory neuropathy caused by mutation in DIAPH3 · auditory neuropathy, autosomal dominant, 1 · auditory neuropathy, autosomal dominant, type 1 · AUNA1 · autosomal dominant auditory neuropathy type 1

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