An instance of hyperlipidemia (disease) that is caused by an inherited modification of the individual's genome.
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cortisone reductase deficiency
MONDO:0000193
hypolipoproteinemia
MONDO:0001822
familial hypercholesterolemia
MONDO:0005439
steroid inherited metabolic disorder
MONDO:0005523
cholesterol-ester transfer protein deficiency
MONDO:0007744
hyperlipidemia, familial combined, LPL related
MONDO:0007759