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 DeCS Categories

C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.147 Blood Protein Disorders .
C15.378.147.607 Hypoproteinemia .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.500 Hypolipoproteinemias .
C16.320.565.398.500.330 Hypoalphalipoproteinemias .
C16.320.565.398.500.440 Hypobetalipoproteinemias .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.500 Dyslipidemias .
C18.452.584.500.500 Hyperlipidemias .
C18.452.584.500.500.644 Hyperlipoproteinemias .
C18.452.584.500.875 Hypolipoproteinemias .
C18.452.584.500.875.330 Hypoalphalipoproteinemias .
C18.452.584.500.875.440 Hypobetalipoproteinemias .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.500 Hypolipoproteinemias .
C18.452.648.398.500.330 Hypoalphalipoproteinemias .
C18.452.648.398.500.440 Hypobetalipoproteinemias .
 Synonyms & Historicals
Hypolipoproteinemias .
Hypolipoproteinemia .
Hypoprebetalipoproteinemia .
Conditions with abnormally low levels of LIPOPROTEINS in the blood. This may involve any of the lipoprotein subclasses, including ALPHA-LIPOPROTEINS (high-density lipoproteins); BETA-LIPOPROTEINS (low-density lipoproteins); and PREBETA-LIPOPROTEINS (very-low-density lipoproteins). .
Hypoproteinemia .
Hypoproteinemias .
A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointestinal tract, EDEMA, or PROTEINURIA. .
Hyperlipoproteinemias .
Hyperlipoproteinemia .
Conditions with abnormally elevated levels of LIPOPROTEINS in the blood. They may be inherited, acquired, primary, or secondary. Hyperlipoproteinemias are classified according to the pattern of lipoproteins on electrophoresis or ultracentrifugation. .
Hypobetalipoproteinemias .
Familial Hypobetalipoproteinemia .
Hypo beta Lipoproteinemia .
Hypobetalipoproteinemia .
Hypo beta Lipoproteinemias .
Conditions with abnormally low levels of BETA-LIPOPROTEINS (low density lipoproteins or LDL) in the blood. It is defined as LDL values equal to or less than the 5th percentile for the population. They include the autosomal dominant form involving mutation of the APOLIPOPROTEINS B gene, and the autosomal recessive form involving mutation of the microsomal triglyceride transfer protein. All are characterized by low LDL and dietary fat malabsorption. .
Hypoalphalipoproteinemias .
Familial High Density Lipoprotein Deficiency Disease .
Familial High-Density Lipoprotein Deficiency Disease .
Familial alpha-Lipoprotein Deficiency Disease .
HDL Cholesterol, Low Serum .
HDL Lipoprotein Deficiency Disease .
High-Density Lipoprotein Deficiency Disease, Familial .
Hypo alpha Lipoproteinemia .
Hypoalphalipoproteinemia .
Hypoalphalipoproteinemia, Primary .
Familial Hypoalphalipoproteinemia .
Familial Hypoalphalipoproteinemias .
Familial alpha Lipoprotein Deficiency Disease .
High Density Lipoprotein Deficiency Disease, Familial .
Hypo alpha Lipoproteinemias .
Hypoalphalipoproteinemias, Familial .
Hypoalphalipoproteinemias, Primary .
Lipoproteinemia, Hypo alpha .
Lipoproteinemias, Hypo alpha .
Primary Hypoalphalipoproteinemias .
alpha Lipoprotein Deficiency Disease, Familial .
alpha Lipoproteinemia, Hypo .
alpha-Lipoprotein Deficiency Disease, Familial .
Hypoalphalipoproteinemia, Familial .
Lipoprotein Deficiency Disease, HDL, Familial .
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. .