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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00154 | Hyperlipoproteinemia, type I | Type I hyperlipoproteinemia is an autosomal recessive disorder caused by deficiency of lipoprotein lipase or its activator apolipoprotein C-II. The defects result in a massive increase in chylomicron and ... | Inherited metabolic disorder |
LPL [HSA:4023] [KO:K01059] APOC2 [HSA:344] [KO:K22287] GPIHBP1 [HSA:338328] [KO:K20001] |
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| H01635 | Hyperlipidemia | Dyslipidemia is a condition characterized by either an increase or decrease in concentration of lipids in the blood. Hyperlipidemia, which refers to an increase in cholesterol, triglyceride (TG), or both ... | Endocrine and metabolic disease |
(Hyperlipoproteinemia type 1) APOC2 [HSA:344] [KO:K22287] (Hyperlipoproteinemia type 1,2) LPL [HSA:4023] [KO:K01059] (Hyperlipoproteinemia type 2) LDLR [HSA:3949] [KO:K12473] (Hyperlipoproteinemia type 5) APOA5 [HSA:116519] [KO:K09025] |
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| H01784 | Primary hyperchylomicronemia | Primary hyperchylomicronemia is characterized by a marked hypertriglyceridemia due to the accumulation of chylomicron. The main clinical symptoms of this disorder are a huge increase in plasma triglyceride ... | Inherited metabolic disorder |
LPL [HSA:4023] [KO:K01059] APOC2 [HSA:344] [KO:K22287] GPIHBP1 [HSA:338328] [KO:K20001] LMF1 [HSA:64788] [KO:K23555] APOA5 [HSA:116519] [KO:K09025] |
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