lipids

3. Genetic disorder causing xanthomas due to defective LDL receptor clearance
5. Signaling lipids derived from omega-3 and omega-6 fatty acids
7. Process by which fatty acids are sequentially cleaved into acetyl-CoA
8. Ketone body produced in excess during uncontrolled diabetes, leading to acidosis
9. Lipoprotein secreted by the intestine to transport dietary lipids
10. Major phospholipid component of mitochondrial membranes
12. Enzyme that esterifies cholesterol within HDL particles
14. Sphingolipid storage disease caused by deficiency of hexosaminidase A

1. Glycerophospholipid critical for surfactant function in the lungs
2. Carrier molecule required for mitochondrial import of long-chain fatty acids
4. Bile acid synthesized from cholesterol, conjugated with glycine or taurine
6. Enzyme that converts acetyl-CoA into malonyl-CoA during fatty acid synthesis
11. Enzyme deficient in Niemann-Pick disease, leading to sphingomyelin accumulation
13. Enzyme that hydrolyzes stored triglycerides in adipocytes, activated by phosphorylation