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Explore conditions, clinical trials, and the organisations running them.
Up to: Inborn errors of metabolism
Inherited lipid metabolism disorder
An inherited metabolic disorder caused by an enzyme deficiency, resulting in an inability to oxidize fatty acids for energy production.
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Lysosomal lipid storage disorder 2 trials · 192 incl. sub-types Sub-types →
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Familial hyperlipidemia 8 trials · 130 incl. sub-types Sub-types →
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Syndromic dyslipidemia 0 trials · 73 incl. sub-types Sub-types →
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Sterol metabolism disorder 0 trials · 60 incl. sub-types Sub-types →
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Steroid inherited metabolic disorder 0 trials · 39 incl. sub-types Sub-types →
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Inherited fatty acid metabolism disorder 7 trials · 21 incl. sub-types Sub-types →
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Disorder of phospholipids, sphingolipids and fatty acids biosynthesis 0 trials · 15 incl. sub-types Sub-types →
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Hypolipoproteinemia 2 trials · 7 incl. sub-types Sub-types →
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Glucocorticoid resistance 3 trials
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CYP7B1-related disorder of oxysterol accumulation 0 trials · 2 incl. sub-types Sub-types →
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Disorder of plasmalogens biosynthesis 0 trials · 2 incl. sub-types Sub-types →
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Inborn disorder of ketolysis 0 trials · 1 incl. sub-types Sub-types →
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Lipoid proteinosis 0 trials