Autosomal dominant nonsyndromic hearing loss 48

MONDO:0011920

Also known as: DFNA48, MYO1A autosomal dominant nonsyndromic deafness, autosomal dominant deafness 48, autosomal dominant nonsyndromic deafness 48, autosomal dominant nonsyndromic deafness type 48, deafness, autosomal dominant 48, deafness, autosomal dominant type 48

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 48 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 48 (0)

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