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

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 6 itself.

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↑ Autosomal dominant nonsyndromic hearing loss (2) ↑ WFS1-related disorder (1)

Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 6 (0)

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