Autosomal recessive nonsyndromic hearing loss 30

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO3A gene.

Also known as: autosomal recessive nonsyndromic hearing loss 30, DFNB30, MYO3A autosomal recessive nonsyndromic deafness, autosomal recessive deafness 30, autosomal recessive nonsyndromic deafness 30, autosomal recessive nonsyndromic deafness caused by mutation in MYO3A, autosomal recessive nonsyndromic deafness type 30, deafness, autosomal recessive 30

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 30 itself.