Hypoalphalipoproteinemia
From Wikipedia, the free encyclopedia
Hypoalphalipoproteinemia Classification and external resources |
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ICD-10 | E78.6 |
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ICD-9 | 272.5 |
OMIM | 604091 |
eMedicine | med/3368 |
MeSH | D052456 |
Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner.[1]
It can be associated with LDL receptor.[2]
[edit] References
- ^ Online 'Mendelian Inheritance in Man' (OMIM) 604091
- ^ Pisciotta L, Calabresi L, Lupattelli G, et al (September 2005). "Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes". Atherosclerosis 182 (1): 153–9. doi: . PMID 16115486.
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