"OMIM mapping confirmed by DO. [SN]."^^ . . _:vb50951133 . "A glycogen storage disease that is characterized by onset of exercise intolerance and muscle cramps in childhood or adolescence and that has_material_basis_in homozygous or compound heterozygous mutation in the PYGM gene, which encodes muscle glycogen phosphorylase, on chromosome 11q13."^^ . . "ICD10CM:E74.04"^^ . "ORDO:368"^^ . "disease_ontology"^^ . "glycogen storage disease V"^^ . "MESH:D006012"^^ . "UMLS_CUI:C0017924"^^ . _:vb50951133 . "GARD:6528"^^ . _:vb50951133 . "Glycogen storage disease, type V"@en . "OMIM:232600"^^ . "McArdle's disease"@en . "SNOMEDCT_US_2021_09_01:55912009"^^ . "DOID:2746"^^ . _:vb50951133 . "NCI:C84738"^^ . . _:vb50951133 . . "myophosphorylase deficiency"@en . . "glycogen storage disease type V"@en .