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Phosphohexose isomerase deficiency

phosphohexose isomerase deficiency phos·pho·hex·ose isomerase deficiency (fŏs’fō-hěk’sōs’)
See glucosephosphate isomerase deficiency.


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  • Phospholipase

    [fos-foh-lahy-peys, -peyz] /ˌfɒs foʊˈlaɪ peɪs, -peɪz/ noun, Biochemistry. 1. any of a group of enzymes that catalyze the breaking down of . phospholipase phos·pho·lip·ase (fŏs’fō-lĭp’ās’, -lī’pās’) n. An enzyme that catalyzes the hydrolysis of a phospholipid. Also called lecithinase.

  • Phospholipid

    [fos-foh-lip-id] /ˌfɒs foʊˈlɪp ɪd/ noun, Biochemistry. 1. any of a group of fatty compounds, as lecithin, composed of phosphoric esters, and occurring in living cells. /ˌfɒsfəˈlɪpɪd/ noun 1. any of a group of compounds composed of fatty acids, phosphoric acid, and a nitrogenous base: important constituents of all membranes Also called phosphatide phospholipid phos·pho·lip·id (fŏs’fō-lĭp’ĭd) […]

  • Phospholipid-bilayer

    noun 1. a two-layered arrangement of phosphate and lipid molecules that form a cell membrane, the hydrophobic lipid ends facing inward and the hydrophilic phosphate ends facing outward.

  • Phosphomutase

    phosphomutase phos·pho·mu·tase (fŏs’fō-myōō’tās, -tāz) n. Any of various enzymes associated with intramolecular transfer catalysis because the donor is regenerated.

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