Autosomal recessive nonsyndromic hearing loss 25

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GRXCR1 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 25, DFNB25, GRXCR1 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 25, autosomal recessive nonsyndromic deafness 25, autosomal recessive nonsyndromic deafness caused by mutation in GRXCR1, autosomal recessive nonsyndromic deafness type 25, deafness, autosomal recessive 25

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 25 itself.