Polyglucosan Body Myopathy 1 with or Without Immunodeficiency, also known as polyglucosan body myopathy type 1, is related to polyglucosan body myopathy 2 and immunodeficiency 57 with autoinflammation, and has symptoms including myalgia An important gene associated with Polyglucosan Body Myopathy 1 with or Without Immunodeficiency is RBCK1 (RANBP2-Type And C3HC4-Type Zinc Finger Containing 1), and among its related pathways/superpathways are p75 NTR receptor-mediated signalling and Toll-like receptor signaling pathway. Affiliated tissues include skeletal muscle and bone, and related phenotypes are scoliosis and ptosis