primary hypoalphalipoproteinemia 1 (DOID:0080957)
Alliance: disease page
Synonyms: familial HDL deficiency; familial hypoalphalipoproteinemia
Alt IDs: OMIM:604091, ORDO:425
Definition: A hypolipoproteinemia that is characterized by low levels of high-density lipoprotein in the blood and that has_material_basis_in heterozygous mutation in the ABC1 gene on chromosome 9q31, which is also the site of mutations causing Tangier disease.