Central Hypoventilation Syndrome, Congenital, 2, and Autonomic Dysfunction (CCHS2)

Central Hypoventilation Syndrome, Congenital, 2, and Autonomic Dysfunction, is also known as cchs2. An important gene associated with Central Hypoventilation Syndrome, Congenital, 2, and Autonomic Dysfunction is MYO1H (Myosin IH). Affiliated tissues include lung, and related phenotypes are dysphagia and global developmental delay