Inborn error of lipid metabolism — Classification and external resources Several fatty acid molecules ICD 10 E75 … Wikipedia
Inborn errors of lipid metabolism — ICD9|277.85 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D008052 Numerous genetic disorders are caused by errors in fatty acid metabolism. These disorders may be described as fatty oxidation disorders or as a lipid… … Wikipedia
Lipid — Structures of some common lipids. At the top are oleic acid[1] and cholesterol.[2] The middle structure is a triglyceride composed of oleoyl, stearoyl, and palmitoyl chains at … Wikipedia
lipid — /lip id, luy pid/, n. Biochem. any of a group of organic compounds that are greasy to the touch, insoluble in water, and soluble in alcohol and ether: lipids comprise the fats and other esters with analogous properties and constitute, with… … Universalium
Metabolism — Cell metabolism redirects here. For the journal, see Cell Metabolism. Structure of adenosine triphosphate, a central intermediate in energy metabolism Metabolism (from Greek: μεταβολή metabolē , change or Greek: μεταβολισμός metabolismos,… … Wikipedia
Lipid storage diseases — A series of disorders due to inborn errors in lipid metabolism resulting in the abnormal accumulation of lipids in the wrong places (Examples include Gaucher, Fabry and Niemann Pick diseases and metachromatic leukodystrophy) … Medical dictionary
lipid granulomatosis — noun widespread xanthomas (especially on elbows and knees); often associated with a disorder of lipid metabolism • Syn: ↑xanthomatosis, ↑xanthoma multiplex, ↑cholesterosis cutis, ↑lipoid granulomatosis • Hypernyms: ↑xanthoma … Useful english dictionary
Lipid signaling — Lipid signaling, broadly defined, refers to any biological signaling event involving a lipid messenger that binds and activates a receptor. Lipid signaling is thought to be qualitatively different from other classical signaling paradigms (such as … Wikipedia
metabolism — /meuh tab euh liz euhm/, n. 1. Biol., Physiol. the sum of the physical and chemical processes in an organism by which its material substance is produced, maintained, and destroyed, and by which energy is made available. Cf. anabolism, catabolism … Universalium
lipid storage disease — Any of a group of relatively rare hereditary disorders of fat metabolism in which enzyme defects cause distinctive types of lipids to accumulate. They include Tay Sachs disease, Gaucher disease, Niemann Pick disease, and Fabry disease. Several… … Universalium
