Congenital insensitivity to pain syndrome, Marsili type

Congenital insensitivity to pain syndrome, Marsili type

Definition

A pain insensitivity disorder in which the cause of the disease is a mutation in ZFHX2 gene. It is characterized by a lowered ability to sense pain, to experience temperature, and to sweat.

Also known as congenital analgesia, autosomal dominant, indifference to pain, congenital, autosomal dominant, insensitivity to pain, congenital, autosomal dominant, MARSILI syndrome, MARSIS — per MONDO

Also identified as