MYH7 and congenital myopathy with cores: Finally, for congenital myopathies, muscle development and calcium homeostasis seem to be the most significant processes, but muscle contraction-related terms also play a role, as well as processes not specific for skeletal muscle, such as catabolism of nucleotides - these appear enriched due to the association of DNM2 to the catabolism of GTP, as well as MYH7 and TPM2 to the catabolism of ATP.