Autosomal recessive nonsyndromic hearing loss 63

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

Also known as: autosomal recessive nonsyndromic hearing loss 63, DFNB63, LRTOMT autosomal recessive nonsyndromic deafness, autosomal recessive deafness 63, autosomal recessive nonsyndromic deafness 63, autosomal recessive nonsyndromic deafness caused by mutation in LRTOMT, autosomal recessive nonsyndromic deafness type 63, deafness, autosomal recessive 63

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 63 itself.