An instance of hyperlipidemia (disease) that is caused by an inherited modification of the individual's genome.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Familial hypercholesterolemia | MONDO:0005439 | 6 | |
| Cholesterol-ester transfer protein deficiency | MONDO:0007744 | CETP | |
| Familial apolipoprotein C-II deficiency | MONDO:0008810 | APOC2 | |
| Familial lipoprotein lipase deficiency | MONDO:0009387 | LPL | |
| Hyperlipidemia due to hepatic triglyceride lipase deficiency | MONDO:0013533 | LIPC | |
| Hyperlipidemia, combined, 2 | MONDO:0011470 | ||
| Hyperlipidemia, familial combined, LPL related | MONDO:0007759 | LPL | |
| Hyperlipoproteinemia type 3 | MONDO:0018473 | ||
| Hyperlipoproteinemia type V | MONDO:0007762 | APOA5 | |
| Hyperlipoproteinemia, type 1D | MONDO:0014412 | GPIHBP1 |
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