has material basis in germline mutation in LIPC familial hyperlipidemia hyperlipidemia due to hepatic triglyceride lipase deficiency https://www.malacards.org/card/hepatic_lipase_deficiency Orphanet:140905 UMLS:C3151466 Hyperlipidemia due to hepatic triacylglycerol lipase deficiency is a rare, genetic hyperalphalipoproteinemia characterized by elevated plasma cholesterol and triglyceride (TG) levels with a marked TG enrichment of low- and high-density lipoproteins (HDL), presence of circulating beta-very low density lipoproteins and elevated HDL cholesterol levels, in the presence of a very low, or undetectable, postheparin plasma hepatic lipase activity. Premature atherosclerosis and/or coronary heart disease may be associated. OMIM:614025 hyperlipidemia due to HL deficiency MONDO:0013533 MEDGEN:462816 SCTID:720940008 GARD:0012864 hyperlipidemia due to hepatic lipase deficiency hyperlipidemia due to HTGL deficiency hyperalphalipoproteinemia