Hypoalphalipoproteinemia

 Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner.^[1]

Hypoalphalipoproteinemia
Hypoalphalipoproteinemia has an autosomal dominant pattern of inheritance.
Specialty	Endocrinology

It can be associated with LDL receptor.^[2]

Associated regions and genes include:

Name	OMIM	Locus	Candidates
HDLCQ1	606613	9p	ABCA1 (Tangier disease)[3]
HDLCQ2	607053	8q23
HDLCQ3	607687	16q24.1	Lecithin cholesterol acyltransferase deficiency (LCAT)
HDLCQ4	610239	4q32
HDLD3	605201	11q23.3	APOA1

niacin is sometimes prescribed to raise HDL levels.^{[citation needed]}