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Disease Ontology Browser
apolipoprotein C-III deficiency (DOID:0111370)
Alliance: disease page
Synonyms: HALP2; hyperalphalipoproteinemia 2
Alt IDs: OMIM:614028
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 APOC3 on chromosome 11q23.3.

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
MGI 6.14
The Jackson Laboratory