Autosomal dominant nonsyndromic hearing loss 6

MONDO:0010963

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the WFS1 gene.

Also known as: DFNA14, DFNA38, DFNA6, WFS1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 14, autosomal dominant deafness 38, autosomal dominant deafness 6, autosomal dominant nonsyndromic deafness 6

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