Autosomal recessive nonsyndromic hearing loss 37

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 37, DFNB37, MYO6 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 37, autosomal recessive nonsyndromic deafness 37, autosomal recessive nonsyndromic deafness caused by mutation in MYO6, autosomal recessive nonsyndromic deafness type 37, deafness, autosomal recessive 37

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 37 itself.