polygenic hypercholesterolemia

polygenic hypercholesterolemia: any of a diverse group of disorders in which some combination of genetic, and frequently also environmental, factors interact to cause elevated plasma cholesterol (i.e., a hyperlipoproteinemia type II-a or II-b phenotype; see table at hyperlipoproteinemia). It is distinguished from familial hypercholesterolemia and familial combined hyperlipidemia.

Игры ⚽ Поможем написать курсовую

Familial hypercholesterolemia — Classification and external resources Xanthelasma palpebrarum, yellowish patches consisting of cholesterol deposits above the eyelids. These are more common in people with FH. ICD … Wikipedia
ABCG5 — Sterolin 1, ABCG5 Größe 651 Aminosäuren Struktur multipass Membranprotein, Heterodimer Bezeichner … Deutsch Wikipedia
ABCG8 — Sterolin 1, ABCG5 Größe 651 Aminosäuren Struktur multipass Membranprotein, Heterodimer Bezeichner … Deutsch Wikipedia
Sterolin — 1, ABCG5 Masse/Länge Primärstruktur 651 Aminosäuren … Deutsch Wikipedia
Genetic disorder — For a non technical introduction to the topic, see Introduction to genetics. Genetic disorder Classification and external resources MeSH D030342 A genetic disorder is an illness caused by abnormalities in genes or … Wikipedia
Nutritional genomics — is a science studying the relationship between human genome, nutrition and health. It can be divided into two disciplines: Nutrigenomics: studies the effect of nutrients on health through altering genome, proteome, metabolome and the resulting… … Wikipedia

Academic Dictionaries and Encyclopedias