Autosomal recessive nonsyndromic hearing loss 39

An autosomal recessive disorder caused by mutations in the HGF gene, encoding hepatocyte growth factor receptor. It is characterized by profound deafness.

Also known as: autosomal recessive nonsyndromic hearing loss 39, DFNB39, HGF autosomal recessive nonsyndromic deafness, autosomal recessive deafness 39, autosomal recessive nonsyndromic deafness 39, autosomal recessive nonsyndromic deafness caused by mutation in HGF, autosomal recessive nonsyndromic deafness type 39, deafness, autosomal recessive 39

3 clinical trials for this condition and its sub-types, 3 tagged with Autosomal recessive nonsyndromic hearing loss 39 itself.