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| Term | cholesterol-ester transfer protein deficiency | ID (Ontology) | DOID:0111368 (Human Disease) |
| Definition | A lipid metabolism disorder characterized by elevated levels of alpha-lipoprotein in the blood. | ||
| Also Known As | "CEPT deficiency" ; "familial hyperalphalipoproteinemia" | ||
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inherited metabolic disorder |__lipid metabolism disorder |__cholesterol-ester transfer protein deficiency |__apolipoprotein C-III deficiency |__hyperalphalipoproteinemia 1 |
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| Is a | lipid metabolism disorder | ||
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| ORDO:79506 | |||