Autosomal recessive nonsyndromic hearing loss 3

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO15A gene.

Also known as: autosomal recessive nonsyndromic hearing loss 3, DFNB3, MYO15A autosomal recessive nonsyndromic deafness, NRSD3, autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3, autosomal recessive nonsyndromic deafness 3, autosomal recessive nonsyndromic deafness caused by mutation in MYO15A, autosomal recessive nonsyndromic deafness type 3

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 3 itself.