Autosomal dominant nonsyndromic hearing loss 30
MONDO:0011673An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 15q25-q26.
Also known as: DFNA30, autosomal dominant deafness 30, autosomal dominant nonsyndromic deafness 30, autosomal dominant nonsyndromic deafness type 30, deafness, autosomal dominant 30
0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 30 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.