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Cholesterol-ester transfer protein deficiency

MONDO:0007744

Also known as: hyperalphalipoproteinemia, CEPT deficiency, familial hyperalphalipoproteinemia, high density lipoprotein cholesterol level QTL 10, hyperalphalipoproteinemia 1, hyperalphalipoproteinemia type 1, CETP deficiency, HALP1

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Hyperlipidemia (295) Metabolic disease (233) Inherited lipid metabolism disorder (189) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Familial hyperlipidemia (8) Hyperlipoproteinemia (8) Disease of genetic or genomic mechanism (2)
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