has material basis in germline mutation in MYH2 inclusion body myositis myopathy, proximal, and ophthalmoplegia https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/congenital_myopathy_6 https://www.malacards.org/card/congenital_myopathy_6_with_ophthalmoplegia GARD:0024809 MEDGEN:381340 DOID:0080719 myopathy, proximal, and ophthalmoplegia MYPOP MESH:C565311 OMIM:605637 MONDO:0011577 myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles UMLS:C1854106 inclusion body myopathy 3, autosomal dominant Any congenital myopathy in which the cause of the disease is a mutation in MYH2 gene. The disorder is either slowly progressive or nonprogressive, and affected individuals retain ambulation, although there is variable severity. It can show both autosomal dominant and autosomal recessive inheritance. inclusion body myopathy 3, autosomal dominant, formerly congenital myopathy