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- B6f88086f02ec2a408e5cf736cf8dae88 hasDbXref "Orphanet:140905" @default.
- B6f88086f02ec2a408e5cf736cf8dae88 type Axiom @default.
- B6f88086f02ec2a408e5cf736cf8dae88 annotatedProperty IAO_0000115 @default.
- B6f88086f02ec2a408e5cf736cf8dae88 annotatedSource MONDO_0013533 @default.
- B6f88086f02ec2a408e5cf736cf8dae88 annotatedTarget "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." @default.