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- Familial_hypertriglyceridemia abstract "Familial hypertriglyceridemia is an autosomal dominant condition occurring in approximately 1% of the population. Triglyceride levels, but not cholesterol, are elevated as a result of excess hepatic production of VLDL or heterozygous LPL deficiency. The condition is associated with premature coronary disease, though treatment sometimes differs from hypercholesterolemia. Affected individuals are at risk for chylomicronemia syndrome, characterized by elevated chylomicrons in the blood. They are also at risk of pancreatitis, especially when triglyceride levels exceed 1000mg/dL.".
- Familial_hypertriglyceridemia wikiPageID "22992129".
- Familial_hypertriglyceridemia wikiPageLength "1167".
- Familial_hypertriglyceridemia wikiPageOutDegree "6".
- Familial_hypertriglyceridemia wikiPageRevisionID "698510760".
- Familial_hypertriglyceridemia wikiPageWikiLink Category:Lipid_metabolism_disorders.
- Familial_hypertriglyceridemia wikiPageWikiLink Category:Skin_conditions_resulting_from_errors_in_metabolism.
- Familial_hypertriglyceridemia wikiPageWikiLink Cutaneous_condition.
- Familial_hypertriglyceridemia wikiPageWikiLink Hyperlipidemia.
- Familial_hypertriglyceridemia wikiPageWikiLink Lipoprotein_lipase_deficiency.
- Familial_hypertriglyceridemia wikiPageWikiLinkText "Familial hypertriglyceridemia".
- Familial_hypertriglyceridemia wikiPageUsesTemplate Template:Cutaneous-condition-stub.
- Familial_hypertriglyceridemia wikiPageUsesTemplate Template:Lipid_metabolism_disorders.
- Familial_hypertriglyceridemia wikiPageUsesTemplate Template:Reflist.
- Familial_hypertriglyceridemia subject Category:Lipid_metabolism_disorders.
- Familial_hypertriglyceridemia subject Category:Skin_conditions_resulting_from_errors_in_metabolism.
- Familial_hypertriglyceridemia hypernym Condition.
- Familial_hypertriglyceridemia type Disease.
- Familial_hypertriglyceridemia type Disorder.
- Familial_hypertriglyceridemia type Error.
- Familial_hypertriglyceridemia type Thing.
- Familial_hypertriglyceridemia type Q12136.
- Familial_hypertriglyceridemia comment "Familial hypertriglyceridemia is an autosomal dominant condition occurring in approximately 1% of the population. Triglyceride levels, but not cholesterol, are elevated as a result of excess hepatic production of VLDL or heterozygous LPL deficiency. The condition is associated with premature coronary disease, though treatment sometimes differs from hypercholesterolemia. Affected individuals are at risk for chylomicronemia syndrome, characterized by elevated chylomicrons in the blood.".
- Familial_hypertriglyceridemia label "Familial hypertriglyceridemia".
- Familial_hypertriglyceridemia sameAs Q5432941.
- Familial_hypertriglyceridemia sameAs m.064pj8r.
- Familial_hypertriglyceridemia sameAs Q5432941.
- Familial_hypertriglyceridemia wasDerivedFrom Familial_hypertriglyceridemia?oldid=698510760.
- Familial_hypertriglyceridemia isPrimaryTopicOf Familial_hypertriglyceridemia.