Human genes for glycerol kinase deficiency
Glycerol kinase deficiency [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.
Synonyms: glycerol kinase deficiency, DOID:0060363, glycerol kinase deficiencies