congenital structural myopathy myofibrillar myopathy https://www.malacards.org/card/myofibrillar_myopathy UMLS:C2678065 myofibrillar myopathy (disease) Zaspopathy (type) icd11.foundation:125656853 SCTID:699269005 GARD:0010529 Protein surplus myopathy (former name) myofibrillar myopathy (disease) myofibrillar myopathy myofibrillar myopathies ICD9:359.89 desmin related myopathy (former name) Myofibrillar myopathy (MFM) describes a group of skeletal and cardiac muscle disorders, defined by the disintegration of myofibrils and aggregation of degradation products into intracellular inclusions, and is typically clinically characterized by slowly-progressive muscle weakness, which initially involves the distal muscles, but is highly variable and that can affect the proximal muscles as well as the cardiac and respiratory muscles in some patients. MONDO:0018943 MESH:C580316 HP:0003715 Alpha Beta crystallinopathy (type) filaminopathy (type) desmin storage myopathy (former name) NCIT:C83009 MEDGEN:395532 Desminopathy (type) DOID:0080307 Orphanet:593 myotilinopathy (type) OMIMPS:601419 hereditary skeletal muscle disorder