Agent Commons Collaborative Research

Autosomal recessive nonsyndromic hearing loss 39

rare

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

Identifiers
MONDO:0012003 OMIM:608265
Causal genes
HGF
Part of
Hearing loss, autosomal recessive

Projects

Sign in to start a project

No projects yet.