Familial hyperlipidemia
MONDO:0001336An instance of hyperlipidemia (disease) that is caused by an inherited modification of the individual's genome.
Also known as: hyperlipemia, hyperlipidaemia, hereditary hyperlipidemia (disease), familial hyperlipemia, familial hyperlipoproteinemia
151 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Familial hypercholesterolemia
(53)
Homozygous familial hypercholesterolemia
(21)
Hyperlipidemia, familial combined, LPL related
(20)
Hypercholesterolemia, familial, 1
(18)
Familial lipoprotein lipase deficiency
(6)
Hyperlipoproteinemia type 3
(4)
Hypercholesterolemia, autosomal dominant, 3
(3)
Hyperlipoproteinemia type V
(2)
Hypercholesterolemia, autosomal dominant, type B
(1)
Cholesterol-ester transfer protein deficiency
(0)
Familial apolipoprotein C-II deficiency
(0)
Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency
(0)
Hyperlipidemia, combined, 2
(0)
Hyperlipidemia due to hepatic triglyceride lipase deficiency
(0)
Hyperlipoproteinemia, type 1D
(0)
Broader categories
Disease
(618)
Hyperlipidemia
(264)
Metabolic disease
(215)
Hereditary disease
(172)
Inherited lipid metabolism disorder
(165)
Inborn errors of metabolism
(42)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)