"NCI:C84585"^^ . "OMIM:302060"^^ . _:vb50936904 . _:vb50936904 . "MESH:D056889"^^ . . . "MESH:D056889"^^ . "OMIM mapping confirmed by DO. [SN]."^^ . "A lipid metabolism disorder that has_material_basis_in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin."^^ . "MGA type II"@en . "disease_ontology"^^ . _:vb50936904 . . "GARD:5890"^^ . "DOID:0050476"^^ . . "ICD10CM:E78.71"^^ . "3-methylglutaconicaciduria type 2"@en . "SNOMEDCT_US_2021_09_01:297231002"^^ . _:vb50936904 . "3-methylglutaconicaciduria type II"@en . _:vb50936904 . . . . "UMLS_CUI:C0574083"^^ . "Barth syndrome"^^ . "MGA Type 2"@en .