Autosomal dominant nonsyndromic hearing loss 16

MONDO:0011389

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 2q23-q24.3.

Also known as: DFNA16, autosomal dominant deafness 16, autosomal dominant nonsyndromic deafness 16, autosomal dominant nonsyndromic deafness type 16, deafness, autosomal dominant 16

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 16 itself.

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↑ Autosomal dominant nonsyndromic hearing loss (2)

Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 16 (0)

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