Term Name:	primary hypoalphalipoproteinemia 1
Synonyms:	familial HDL deficiency
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.
Ontology:	Human Disease [DOID:0080957]   ( DOID:0080957 )