Autosomal dominant nonsyndromic hearing loss 43

MONDO:0012030

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

Also known as: DFNA43, autosomal dominant deafness 43, autosomal dominant nonsyndromic deafness 43, autosomal dominant nonsyndromic deafness type 43, deafness, autosomal dominant 43

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 43 itself.

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↑ Autosomal dominant nonsyndromic hearing loss (2)

Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 43 (0)

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