"disease_ontology"^^ . . "DOID:0080687"^^ . _:vb50941445 . _:vb50941445 . "A myopathy that is characterized by by the presence of intracytoplasmic inclusion bodies strongly stained by menadione-linked alpha-glycerophosphate dehydrogenase in the absence of substrate, alpha-glycerophosphate, with late childhood or adult onset, and that has_material_basis_in mutation in the FHL1 gene on chromosome Xq26."^^ . . "OMIM:300718"^^ . _:vb50941445 . "reducing body myopathy 1B"@en . _:vb50941445 . _:vb50941445 . . .