C0002768 - A very rare, autosomal recessive inherited condition caused by mutations in the SCN9A gene. It is characterized by a lack of the ability to perceive physical pain.

C0002768 - A very rare, autosomal recessive inherited condition caused by mutations in the SCN9A gene. It is characterized by a lack of the ability to perceive physical pain. Sorry, but the limit is exceeded! Please try again after 1 min...C0002768