Autosomal dominant nonsyndromic hearing loss 59

MONDO:0012974

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 11p14.2-q12.3.

Also known as: DFNA59, autosomal dominant deafness 59, autosomal dominant nonsyndromic deafness 59, autosomal dominant nonsyndromic deafness type 59, deafness, autosomal dominant 59

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 59 itself.

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↑ Autosomal dominant nonsyndromic hearing loss (2)

Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 59 (0)

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