Hypoalphalipoproteinemia
Infobox_Disease
Name = PAGENAME
Caption =
DiseasesDB =
ICD10 = ICD10|E|78|6|e|70
ICD9 = ICD9|272.5
ICDO =
OMIM = 604091
MedlinePlus =
eMedicineSubj = med
eMedicineTopic = 3368
MeshID = D052456
Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner. [OMIM|604091]
It can be associated with LDL receptor.[cite journal |author=Pisciotta L, Calabresi L, Lupattelli G, "et al" |title=Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes |journal=Atherosclerosis |volume=182 |issue=1 |pages=153–9 |year=2005 |month=September |pmid=16115486 |doi=10.1016/j.atherosclerosis.2005.01.048 |url=http://linkinghub.elsevier.com/retrieve/pii/S0021-9150(05)00117-6] ]References
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