/autosomal recessive nonsyndromic hearing loss 39

autosomal recessive nonsyndromic hearing loss 39

Rare Disease

MONDO:0012003

Also Known As

autosomal recessive nonsyndromic hearing loss 39DFNB39HGF autosomal recessive nonsyndromic deafnessautosomal recessive deafness 39autosomal recessive nonsyndromic deafness 39autosomal recessive nonsyndromic deafness caused by mutation in HGFautosomal recessive nonsyndromic deafness type 39deafness, autosomal recessive 39deafness, autosomal recessive type 39

Definition

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