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Disease Ontology Browser
hyperalphalipoproteinemia 1 (DOID:0111369)
Alliance: disease page
Synonyms: HALP1
Alt IDs: OMIM:143470, MESH:C564591, NCI:C128806, UMLS_CUI:C0342883
Definition: A cholesterol-ester transfer protein deficiency characterized by elevated levels of alpha-lipoprotein in the blood that has_material_basis_in heterozygous mutation in the CETP gene on chromosome 16q13.

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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory