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- Q2349695 subject Q6853484.
- Q2349695 subject Q8591772.
- Q2349695 subject Q8750387.
- Q2349695 abstract "Lipoprotein lipase deficiency (also known as "familial chylomicronemia syndrome", "chylomicronemia", "chylomicronemia syndrome" and "hyperlipoproteinemia type Ia") is a rare autosomal recessive lipid disorder 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.".
- Q2349695 icd10 "E78".
- Q2349695 meshId "D008072".
- Q2349695 omim "238600".
- Q2349695 wikiPageExternalLink fcs.raredr.com.
- Q2349695 wikiPageExternalLink content.aspx?sectionid=62637184&bookid=971&Resultclick=2&q=Lipoprotein+Lipase+Deficiency.
- Q2349695 wikiPageExternalLink NBK1308.
- Q2349695 wikiPageExternalLink lipoprotein-lipase-deficiency.
- Q2349695 wikiPageWikiLink Q1079120.
- Q2349695 wikiPageWikiLink Q11358.
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- Q2349695 wikiPageWikiLink Q641605.
- Q2349695 wikiPageWikiLink Q6531938.
- Q2349695 wikiPageWikiLink Q6853484.
- Q2349695 wikiPageWikiLink Q76560.
- Q2349695 wikiPageWikiLink Q8591772.
- Q2349695 wikiPageWikiLink Q8750387.
- Q2349695 wikiPageWikiLink Q954845.
- Q2349695 wikiPageWikiLink Q955332.
- Q2349695 icd "E78".
- Q2349695 meshid "D008072".
- Q2349695 name "Lipoprotein lipase deficiency".
- Q2349695 omim "238600".
- Q2349695 type Disease.
- Q2349695 type Thing.
- Q2349695 type Q12136.
- Q2349695 comment "Lipoprotein lipase deficiency (also known as "familial chylomicronemia syndrome", "chylomicronemia", "chylomicronemia syndrome" and "hyperlipoproteinemia type Ia") is a rare autosomal recessive lipid disorder 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.".
- Q2349695 label "Lipoprotein lipase deficiency".
- Q2349695 name "Lipoprotein lipase deficiency".