DO_rare_slim DO_FlyBase_slim disease has basis in glycerol kinase deficiency ORDO:408 SNOMEDCT_US_2025_09_01:297256008 2015-09-17T15:45:20Z MIM:307030 UMLS_CUI:C0574108 DOID:0060363 An inherited metabolic disorder characterized_by wide range of phenotypic variability; patients can have severe metabolic and CNS abnormalities, while others possess hyperglycerolemia and glyceroluria with no other apparent phenotype and that has_material_basis_in mutation in the GK gene on chromosome Xp21. disease_ontology inherited metabolic disorder structural_variant