Autosomal dominant nonsyndromic hearing loss 41

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the P2RX2 gene.

Also known as: DFNA41, P2RX2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 41, autosomal dominant nonsyndromic deafness 41, autosomal dominant nonsyndromic deafness caused by mutation in P2RX2, autosomal dominant nonsyndromic deafness type 41, deafness, autosomal dominant 41, deafness, autosomal dominant type 41

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 41 itself.