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| {{Infobox_Disease |
| | #Redirect [[Low HDL]] |
| Name = {{PAGENAME}} |
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| Image = |
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| Caption = |
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| DiseasesDB = |
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| ICD10 = {{ICD10|E|78|6|e|70}} |
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| ICD9 = {{ICD9|272.5}} |
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| ICDO = |
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| OMIM = 604091 |
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| MedlinePlus = |
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| eMedicineSubj = med |
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| eMedicineTopic = 3368 |
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| MeshID = D052456 |
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| }}
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| {{SI}}
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| {{CMG}}
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| '''Hypoalphalipoproteinemia''' is a [[high-density lipoprotein]] deficiency, inherited in an [[autosomal]] [[dominant]] manner.<ref>{{OMIM|604091}}</ref>
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| [[Image:autodominant.jpg|thumb|left|{{PAGENAME}} has an autosomal dominant pattern of [[inheritance]].]]
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| It can be associated with [[LDL receptor]].<ref name="pmid16115486">{{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}}</ref>
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| ==References==
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| {{reflist|2}}
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| {{Lipidemias}}
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| [[Category:Genetic disorders]]
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