Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Hypertriglyceridemia

Hypertriglyceridemia is a lipid disorder characterized by elevated triglycerides.

Systematic

Hyperlipemia
Chylomicronemia
Familial combined Hyperlipemia
Hypercholesterolemia
Hypertriglyceridemia
APOA5
APOE
Combined lipase deficiency
LMF1
GPIHBP1
LIPC
LIPE
LPL
Plasma triglyceride level quantitative trait locus
ANGPTL4
Transient infantile hypertriglyceridemia
GPD1
Lysosomal acid lipase deficiency

References:

1.

Karathanasis SK et al. () Linkage of human apolipoproteins A-I and C-III genes.

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2.

Kao JT et al. (2003) A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia.

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3.

Breckenridge WC et al. (1978) Hypertriglyceridemia associated with deficiency of apolipoprotein C-II.

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4.

Goldstein JL et al. (1973) Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia.

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5.

Duggirala R et al. (2000) A major susceptibility locus influencing plasma triglyceride concentrations is located on chromosome 15q in Mexican Americans.

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6.

Brunzell JD et al. (1975) Evidence for diabetes mellitus and genetic forms of hypertriglyceridemia as independent entities.

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7.

Wen XY et al. (2003) Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans.

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8.

Johansen CT et al. (2010) Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.

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9.

Namboodiri KK et al. (1977) Segregation and linkage analyses of a large pedigree with hypertriglyceridemia.

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10.

Glueck CJ et al. (1980) Pancreatitis, familial hypertriglyceridemia, and pregnancy.

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11.

Orphanet article

Orphanet ID 300293 [^]
12.

OMIM.ORG article

Omim 145750 [^]
13.

Wikipedia article

Wikipedia EN (Hypertriglyceridemia) [^]
Update: April 29, 2019