C1704417 - Type IIb hyperlipoproteinemia is caused by mutation in the receptor-binding domain of APOLIPOPROTEIN B-100 which is a major component of LOW-DENSITY LIPOPROTEINS and VERY-LOW-DENSITY LIPOPROTEINS resulting in reduced clearance of these lipoproteins. It is characterized by both hypercholesterolemia and HYPERTRIGLYCERIDEMIA (combined hyperlipidemia). 1/10
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Terms, descriptions
CUI    C1704417
RussianMDRRUS 10045264 L16082284preferred S19403157 Y Гиперлипопротеинемия IIb типа
RussianMDRRUS 10017345 L16061260no S19403161 Y Гиперлипопротеинемия Фредриксона IIb типа
RussianMDRRUS 10054676 L16113793no S19403166 Y Гиперлипопротеинемия типа IIb
RussianMDRRUS 10060598 L16124306no S19403165 Y Гиперлипопротеинемия типа IIb по Фредриксону
Medical Subject Headings A26620040 AT64676349 Type IIb hyperlipoproteinemia is caused by mutation in the receptor-binding domain of APOLIPOPROTEIN B-100 which is a major component of LOW-DENSITY LIPOPROTEINS and VERY-LOW-DENSITY LIPOPROTEINS resulting in reduced clearance of these lipoproteins. It is characterized by both hypercholesterolemia and HYPERTRIGLYCERIDEMIA (combined hyperlipidemia).