Familial hyperchylomicronemia: Difference between revisions
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{{SK}} Type I hyperlipoproteinemia, | {{SK}} Type I hyperlipoproteinemia, Burger-Grutz syndrome, primary hyperlipoproteinemia, lipoprotein lipase deficiency, LPL deficiency, idiopathic hyperlipemia, essential hyperlipemia, familial hyperlipemia, lipase D deficiency, hyperlipoproteinemia type IA, familial chylomicronemia | ||
{{PleaseHelp}} | {{PleaseHelp}} | ||
{{Lipopedia}} | {{Lipopedia}} | ||
[[Category:Lipopedia]] | [[Category:Lipopedia]] |
Revision as of 20:37, 12 September 2013
Synonyms and keywords: Type I hyperlipoproteinemia, Burger-Grutz syndrome, primary hyperlipoproteinemia, lipoprotein lipase deficiency, LPL deficiency, idiopathic hyperlipemia, essential hyperlipemia, familial hyperlipemia, lipase D deficiency, hyperlipoproteinemia type IA, familial chylomicronemia
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