Congenital Myopathy 24, also known as nemaline myopathy 11, autosomal recessive, is related to nemaline myopathy 11 and nemaline myopathy. An important gene associated with Congenital Myopathy 24 is MYPN (Myopalladin). Affiliated tissues include skeletal muscle and heart, and related phenotypes are muscle weakness and type 1 muscle fiber predominance