Autosomal dominant nonsyndromic hearing loss 4A

MONDO:0010915

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH14 gene.

Also known as: DFNA4A, MYH14 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 4A, autosomal dominant nonsyndromic deafness 4A, autosomal dominant nonsyndromic deafness caused by mutation in MYH14, autosomal dominant nonsyndromic deafness type 4A, deafness, autosomal dominant 4, deafness, autosomal dominant 4A

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 4A itself.

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