Английская Википедия:Hypoalphalipoproteinemia
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Шаблон:Infobox medical condition (new) Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner.[1]
It can be associated with LDL receptor.[2]
Associated regions and genes include:
Name | OMIM | Locus | Candidates |
---|---|---|---|
HDLCQ1 | Шаблон:OMIM | 9p | ABCA1 (Tangier disease)[3] |
HDLCQ2 | Шаблон:OMIM | 8q23 | |
HDLCQ3 | Шаблон:OMIM | 16q24.1 | Lecithin cholesterol acyltransferase deficiency (LCAT) |
HDLCQ4 | Шаблон:OMIM | 4q32 | |
HDLD3 | Шаблон:OMIM | 11q23.3 | APOA1 |
niacin is sometimes prescribed to raise HDL levels.Шаблон:Cn
References
External links
Шаблон:Medical resources Шаблон:Lipidemias