DISEASES

Disease-gene associations mined from literature

Human genes for familial hypertriglyceridemia

Familial hypertriglyceridemia [DOID:0050527]

A lipid metabolism disorder characterized by elevated triglyceride levels as a result of excess hepatic production of VLDL or heterozygous LPL deficiency.

Synonyms:  familial hypertriglyceridemia,  DOID:0050527,  Pure hyperglyceridemia

Linkouts:  OMIM