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・ Lipophrys pholis
・ Lipophrys trigloides
・ Lipoplatin
・ Lipopolysaccharide
・ Lipopolysaccharide 3-alpha-galactosyltransferase
・ Lipopolysaccharide binding protein
・ Lipopolysaccharide glucosyltransferase I
・ Lipopolysaccharide glucosyltransferase II
・ Lipopolysaccharide kinase (Kdo/WaaP) family
・ Lipopolysaccharide N-acetylglucosaminyltransferase
・ Lipopolysaccharide N-acetylmannosaminouronosyltransferase
・ Lipopolysaccharide-transporting ATPase
・ LipoProfile
・ Lipoprotein
・ Lipoprotein lipase
Lipoprotein lipase deficiency
・ Lipoprotein receptor-related protein
・ Lipoprotein(a)
・ Lipoprotein-associated phospholipase A2
・ Lipoprotein-X
・ Lipoptena
・ Lipoptena cervi
・ Lipoptena depressa
・ Lipoptena mazamae
・ Lipopteninae
・ Lipopterichthys carrioni
・ Lipopterocis
・ Liposarcoma
・ Liposcelididae
・ Liposcelis bostrychophila


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Lipoprotein lipase deficiency : ウィキペディア英語版
Lipoprotein lipase deficiency

Lipoprotein lipase deficiency (also known as "(familial chylomicronemia syndrome )", "chylomicronemia",〔 "chylomicronemia syndrome" and "hyperlipoproteinemia type Ia"〔, updated 03/18/2004. As of October 2012, mention of type Ia no longer appears in the OMIM record.〕) is caused by a mutation in the gene which codes lipoprotein lipase. As a result, afflicted individuals lack the ability to produce lipoprotein lipase enzymes necessary for effective breakdown of fatty acids.
==Incidence==
The disorder affects about 1 out of 1,000,000 people.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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