cap myopathy https://rarediseases.info.nih.gov/diseases/11915/cap-myopathy https://www.malacards.org/card/cap_myopathy SCTID:703532002 GARD:0011915 MEDGEN:777197 Orphanet:171881 MONDO:0015753 MESH:C579969 Cap disease UMLS:C3710589 Cap myopathy is a very rare congenital myopathy presenting a weakness of facial and respiratory muscles associated with craniofacial and thoracic deformities, as well as weakness of limb proximal and distal muscles. Onset is at birth or in childhood, weakness progression is slow but may lead to a severe and even fatal prognosis. congenital myopathy with caps alpha-actinopathy TPM3-related myopathy