Hypoalphalipoproteinemias

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.

Also Known As:

Hypoalphalipoproteinemia; Familial High-Density Lipoprotein Deficiency Disease; Familial alpha-Lipoprotein Deficiency Disease; HDL Lipoprotein Deficiency Disease; High-Density Lipoprotein Deficiency Disease, Familial; Hypo alpha Lipoproteinemia; Familial High Density Lipoprotein Deficiency Disease; Familial Hypoalphalipoproteinemia; Familial Hypoalphalipoproteinemias; Familial alpha Lipoprotein Deficiency Disease; High Density Lipoprotein Deficiency Disease, Familial; Hypo alpha Lipoproteinemias; Hypoalphalipoproteinemias, Familial; alpha Lipoprotein Deficiency Disease, Familial; Hypoalphalipoproteinemia, Familial; Lipoprotein Deficiency Disease, HDL, Familial; alpha-Lipoprotein Deficiency Disease, Familial

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Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 449

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Inborn Genetic Diseases: 578

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Inborn Errors Metabolism: 434

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Inborn Errors Lipid Metabolism

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Hypolipoproteinemias: 25

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Hypoalphalipoproteinemias: 135

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Nutritional and Metabolic Diseases

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Metabolic Diseases: 1406

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Inborn Errors Metabolism: 434

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Inborn Errors Lipid Metabolism

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Hypolipoproteinemias: 25

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Hypoalphalipoproteinemias: 135

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Lipid Metabolism Disorders: 92

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Dyslipidemias: 4230

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Hypolipoproteinemias: 25

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Hypoalphalipoproteinemias: 135

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