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Summary Literature (0)
DOID:0111369 - hyperalphalipoproteinemia 1


Disease Ontology 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.

Synonyms: HALP1,

Xenbase Genes : cetp



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), cholesterol-ester transfer protein deficiency (is_a)