Autosomal recessive nonsyndromic hearing loss 77

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LOXHD1 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 77, DFNB77, LOXHD1 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 77, autosomal recessive nonsyndromic deafness 77, autosomal recessive nonsyndromic deafness caused by mutation in LOXHD1, autosomal recessive nonsyndromic deafness type 77, deafness, autosomal recessive 77

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 77 itself.