| Topical term | hyperlipoproteinémia typu I - BL - CF - CI - CL - CO - DG - DH - DI - DT - EC - EH - EM - EN - EP - ET - GE - HI - IM - ME - MI - MO - NU - PA - PC - PP - PS - PX - RH - RT - SU - TH - UR - VE - VI
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| Other term | Apolipoprotein C-II Deficiency
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| Hyperchylomicronemia, Familial
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| Lipoprotein Lipase Deficiency, Familial
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| deficit apolipoproteínu C-II
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| hyperchylomikronémia familiárna
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| deficit lipoproteínlipázy, familiárny
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| deficit lipoproteínovej lipázy, familiárny
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| deficiencia lipoproteínovej lipázy, familiárna
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| hyperlipoproteinémia, typ Ia
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| hyperlipoproteinémia, typ Ib
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| hyperlipoproteinémia, typ I
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| hyperchylomikronémia familiárna
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| hyperchylomikronémia familiárna esenciálna
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| chylomikronémia familiárna
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| C-II anapolipoproteinémia
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| deficit lipázy D
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| nedostatok apolipoproteínu C-II
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| Burger-Grutzov syndróm
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| hypertriglyceridémia familiárna, indukovaná tukmi
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| hyperlipoproteinémia familiárna, typ 1
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| deficiencia LPL
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| hyperlipémia idiopatická, Burger-Grutzov typ
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| deficiencia LIPD
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| deficiencia lipázy D
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| deficiencia lipoproteínovej lipázy
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| See also | (b) lipoproteínlipáza
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| (p) lipoproteínlipáza
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| (p) apolipoproteín C-II
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| (b) apolipoproteín C-II
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| Collection kind | t150m - MeSH descriptor
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| References | (2) Authority database - MeSH descriptor
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| (3) Catalogue documents - CiBaMed
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| (9) Catalogue documents - Articles
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| (2) Catalogue documents - Books
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