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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01199 | Hyperalphalipoproteinemia | ... genetic and environmental factors. The most important cause of primary HALP is a genetic deficiency of CETP, which has been reported mainly from Japan. A mutation in APOC3 gene is also associated in some ... | Inherited metabolic disorder |
(HALP1) CETP [HSA:1071] [KO:K16835] (HALP2) APOC3 [HSA:345] [KO:K08759] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |