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... > Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Lipid Metabolism, Inborn Errors > Hypolipoproteinemias > Hypoalphalipoproteinemias
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Hypolipoproteinemias > Hypoalphalipoproteinemias
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Hypolipoproteinemias > Hypoalphalipoproteinemias
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Dyslipidemias > Hypolipoproteinemias > Hypoalphalipoproteinemias

Preferred term

Hypoalphalipoproteinemias  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Entry terms

  • alpha Lipoproteinemia, Hypo
  • HDL Cholesterol, Low Serum
  • Hypo alpha Lipoproteinemia
  • Hypoalphalipoproteinemia
  • Hypo alpha Lipoproteinemias
  • Lipoproteinemia, Hypo alpha
  • Lipoproteinemias, Hypo alpha

Scope note

  • 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.

History note

  • 2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL use TANGIER DISEASE 1995-2006

In other languages

  • hypoalfalipoproteinemiat

    Finnish

  • deficientia acyltransferasae lecithin-cholesteroli
  • hypo-alfa-lipoproteinemi
  • hypoalfalipoproteinemia
  • hypoalphalipoproteinaemia
  • LCAT-puutos
  • lecitin-kolesterol-akyltransferasbrist
  • lesitiini-kolesteroli-asyylitransferaasin (LCAT) puutos
  • lesitiini-kolesteroli-asyylitransferaasin puutos
  • morbus Tangier
  • Tangierin tauti
  • Tangiers sjuka
  • Hypoalfalipoproteinemier

    Swedish

URI

http://www.yso.fi/onto/mesh/D052456

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