Autosomal dominant nonsyndromic hearing loss 58

MONDO:0014293

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 2p21-p12.

Also known as: DFNA58, autosomal dominant deafness 58, autosomal dominant nonsyndromic deafness 58, autosomal dominant nonsyndromic deafness type 58, deafness, autosomal dominant 58

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 58 itself.

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Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 58 (0)

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