Autosomal dominant nonsyndromic hearing loss 18

MONDO:0011625

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 3q22.

Also known as: DFNA18, autosomal dominant deafness 18, autosomal dominant nonsyndromic deafness 18, autosomal dominant nonsyndromic deafness type 18, deafness, autosomal dominant 18

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 18 itself.

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↑ Autosomal dominant nonsyndromic hearing loss (2)

Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 18 (0)

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