Human genes for hyperalphalipoproteinemia 1
Hyperalphalipoproteinemia 1 [DOID:0111369]
A cholesterol-ester transfer protein deficiency characterized by elevated levels of alpha-lipoprotein in the blood that has_material_basis_in heterozygous mutation in CETP on chromosome 16q13.
Synonyms: hyperalphalipoproteinemia 1, DOID:0111369, HALP1