Number of the records: 1
hyperlipoproteinémia typu I
Record number d008072 Date 06.06.2025 Type M - MESH Topical term hyperlipoproteinémia typu I Other term English (Pseudonym) Apolipoprotein C-II Deficiency
English (Pseudonym) Hyperchylomicronemia, Familial
English (Pseudonym) Lipoprotein Lipase Deficiency, Familial
Slovak (Pseudonym) deficit apolipoproteínu C-II
Slovak (Pseudonym) hyperchylomikronémia familiárna
Slovak (Pseudonym) deficit lipoproteínlipázy, familiárny
Slovak (Pseudonym) deficit lipoproteínovej lipázy, familiárny
Slovak (Pseudonym) deficiencia lipoproteínovej lipázy, familiárna
Slovak (Pseudonym) hyperlipoproteinémia, typ Ia
Slovak (Pseudonym) hyperlipoproteinémia, typ Ib
Slovak (Pseudonym) hyperlipoproteinémia, typ I
Slovak (Pseudonym) hyperchylomikronémia familiárna
Slovak (Pseudonym) hyperchylomikronémia familiárna esenciálna
Slovak (Pseudonym) chylomikronémia familiárna
Slovak (Pseudonym) C-II anapolipoproteinémia
Slovak (Pseudonym) deficit lipázy D
Slovak (Pseudonym) nedostatok apolipoproteínu C-II
Slovak (Pseudonym) Burger-Grutzov syndróm
Slovak (Pseudonym) hypertriglyceridémia familiárna, indukovaná tukmi
Slovak (Pseudonym) hyperlipoproteinémia familiárna, typ 1
Slovak (Pseudonym) deficiencia LPL
Slovak (Pseudonym) hyperlipémia idiopatická, Burger-Grutzov typ
Slovak (Pseudonym) deficiencia LIPD
Slovak (Pseudonym) deficiencia lipázy D
Slovak (Pseudonym) deficiencia lipoproteínovej lipázy
See also (Later heading) lipoproteínlipáza
(Skutočné meno) lipoproteínlipáza
(Skutočné meno) apolipoproteín C-II
(Later heading) apolipoproteín C-II
UDC C16.320.565.398.465C18.452.584.500.500.644.237C18.452.584.563.465C18.452.648.398.465 Note An 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. 
subject heading
Number of the records: 1