Congenital Myopathy 10b, Mild Variant (CMYP10B)

Congenital Myopathy 10b, Mild Variant, also known as myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant, is related to congenital myopathy 10a, severe variant. An important gene associated with Congenital Myopathy 10b, Mild Variant is MEGF10 (Multiple EGF Like Domains 10). Affiliated tissues include skeletal muscle, and related phenotypes are scoliosis and dysphagia