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hyperlipoproteinémia typu I

  1. Subject h.hyperlipoproteinémia typu I
    Subject h.Hyperlipoproteinemia Type I
    Entry termsdeficit apolipoproteínu C-II
    hyperchylomikronémia familiárna
    deficit lipoproteínlipázy, familiárny
    deficit lipoproteínovej lipázy, familiárny
    deficiencia lipoproteínovej lipázy, familiárna
    hyperlipoproteinémia, typ Ia
    hyperlipoproteinémia, typ Ib
    hyperlipoproteinémia, typ I
    hyperchylomikronémia familiárna
    hyperchylomikronémia familiárna esenciálna
    chylomikronémia familiárna
    C-II anapolipoproteinémia
    deficit lipázy D
    nedostatok apolipoproteínu C-II
    Burger-Grutzov syndróm
    hypertriglyceridémia familiárna, indukovaná tukmi
    hyperlipoproteinémia familiárna, typ 1
    deficiencia LPL
    hyperlipémia idiopatická, Burger-Grutzov typ
    deficiencia LIPD
    deficiencia lipázy D
    deficiencia lipoproteínovej lipázy
    English X referencesApolipoprotein C-II Deficiency
    Hyperchylomicronemia, Familial
    Lipoprotein Lipase Deficiency, Familial
    Scope note in EnglishAn inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing.
    See also reference (FX) in Slovak apolipoproteín C-II
    lipoproteínlipáza
    See also reference (FX) in English Apolipoprotein C-II
    Lipoprotein Lipase
    Links (9) - ARTICLES
    (2) - MeSH descriptor
    (2) - CiBaMed
    (2) - BOOKS
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Number of the records: 1  

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