Autosomal dominant nonsyndromic hearing loss 47

MONDO:0012090

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 9p22-p21.

Also known as: DFNA47, autosomal dominant deafness 47, autosomal dominant nonsyndromic deafness 47, autosomal dominant nonsyndromic deafness type 47, deafness, autosomal dominant 47

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 47 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal dominant nonsyndromic hearing loss (2)

Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 47 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.