Concept information
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Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypoalphalipoproteinemias
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Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypoalphalipoproteinemias
Término preferido
Tangier Disease
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Tipo
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mesh:Descriptor
Definición
- An autosomal recessively inherited disorder caused by mutation of ATP-BINDING CASSETTE TRANSPORTERS involved in cellular cholesterol removal (reverse-cholesterol transport). It is characterized by near absence of ALPHA-LIPOPROTEINS (high-density lipoproteins) in blood. The massive tissue deposition of cholesterol esters results in HEPATOMEGALY; SPLENOMEGALY; RETINITIS PIGMENTOSA; large orange tonsils; and often sensory POLYNEUROPATHY. The disorder was first found among inhabitants of Tangier Island in the Chesapeake Bay, MD.
Concepto genérico
Etiquetas alternativas
- Alpha High Density Lipoprotein Deficiency Disease
- Analphalipoproteinemia
- Cholesterol Thesaurismosis
- HDLDT1
- High Density Lipoprotein Deficiency, Tangier Type
- High Density Lipoprotein Deficiency, Type 1
- High-Density Lipoprotein Deficiency, Tangier Type
- High-Density Lipoprotein Deficiency, Type I
En otras lenguas
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francés
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Analphalipoprotéinémie
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Déficit familial en HDL de type 1
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Déficit familial en HDL de type I
URI
http://data.loterre.fr/ark:/67375/JVR-T6QJ6LLL-5
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