Familial hyperchylomicronemia: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{SK}} Type I hyperlipoproteinemia, Buerger-Gruetz syndrome, primary 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

Please help WikiDoc by adding content here. It's easy! Click here to learn about editing.