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Disease Ontology Browser
cholesterol-ester transfer protein deficiency (DOID:0111368)
Alliance: disease page
Synonyms: CEPT deficiency; familial hyperalphalipoproteinemia
Alt IDs: ORDO:79506
Definition: A lipid metabolism disorder characterized by elevated levels of alpha-lipoprotein in the blood.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
05/10/2022
MGI 6.19
The Jackson Laboratory