Autosomal dominant nonsyndromic hearing loss 2B

MONDO:0012976

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GJB3 gene.

Also known as: DFNA2B, GJB3 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 2B, autosomal dominant nonsyndromic deafness 2B, autosomal dominant nonsyndromic deafness caused by mutation in GJB3, autosomal dominant nonsyndromic deafness type 2B, deafness, autosomal dominant 2B, deafness, autosomal dominant 2b

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 2B 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 2B (0)

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