Autosomal dominant nonsyndromic hearing loss 10

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the EYA4 gene.

Also known as: autosomal dominant nonsyndromic hearing loss 10, DFNA10, EYA4 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 10, autosomal dominant nonsyndromic deafness 10, autosomal dominant nonsyndromic deafness caused by mutation in EYA4, autosomal dominant nonsyndromic deafness type 10, deafness, autosomal dominant 10

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