Autosomal dominant nonsyndromic hearing loss 28

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GRHL2 gene.

Also known as: DFNA28, GRHL2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 28, autosomal dominant nonsyndromic deafness 28, autosomal dominant nonsyndromic deafness caused by mutation in GRHL2, autosomal dominant nonsyndromic deafness type 28, deafness, autosomal dominant 28, deafness, autosomal dominant type 28

60 clinical trials for this condition and its sub-types.