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Hypoalphalipoproteinemias

More information in Books or onNLM PubMed
Definition: Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS.     
Examples Lecithin Acyltransferase Deficiency; Tangier Disease
Other names alpha Lipoproteinemia, Hypo; alpha Lipoprotein Deficiency Disease, Familial; Primary Hypoalphalipoproteinemias; Primary Hypoalphalipoproteinemia; Lipoproteinemias, Hypo alpha; Lipoproteinemia, Hypo alpha; Hypoalphalipoproteinemias, Primary; Hypoalphalipoproteinemias, Familial; High Density Lipoprotein Deficiency Disease, Famil; Hypo alpha Lipoproteinemias; Familial alpha Lipoprotein Deficiency Disease; Familial Hypoalphalipoproteinemias; Familial Hypoalphalipoproteinemia; Familial High Density Lipoprotein Deficiency Disea; Hypoalphalipoproteinemia, Primary; Hypoalphalipoproteinemia; Hypo alpha Lipoproteinemia; High-Density Lipoprotein Deficiency Disease, Famil; HDL Lipoprotein Deficiency Disease; Familial alpha-Lipoprotein Deficiency Disease
 
SubstanceCAS Registry & nameCategoriesSource
Familial HDL deficiency  0   *Hypoalphalipoproteinemias.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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