Hypoalphalipoproteinemia
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| Hypoalphalipoproteinemia | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | E78.6 |
| ICD-9-CM | 272.5 |
| OMIM | 604091 |
| eMedicine | med/3368 |
| Patient UK | Hypoalphalipoproteinemia |
| MeSH | D052456 |
Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner.[1]
Hypoalphalipoproteinemia has an autosomal dominant pattern of inheritance.
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.
References
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- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 604091
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
