Autosomal recessive nonsyndromic hearing loss 51
MONDO:0012370An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 11p13-p12.
Also known as: DFNB51, autosomal recessive deafness 51, autosomal recessive nonsyndromic deafness 51, autosomal recessive nonsyndromic deafness type 51, deafness, autosomal recessive 51
0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 51 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.