Autosomal recessive nonsyndromic hearing loss 97

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

Also known as: DFNB97, MET autosomal recessive nonsyndromic deafness, autosomal recessive deafness 97, autosomal recessive nonsyndromic deafness 97, autosomal recessive nonsyndromic deafness caused by mutation in MET, autosomal recessive nonsyndromic deafness type 97, deafness, autosomal recessive 97, deafness, autosomal recessive type 97

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 97 itself.