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Up to: Inherited lipid metabolism disorder · Lysosomal storage disease
Lysosomal lipid storage disorder
An inherited metabolic disorder in which harmful amounts of lipids accumulate in cells and tissues. Because of a functionally impaired hydrolase or auxiliary protein, their lipid substrates cannot be degraded, accumulate in the lysosome, and slowly spread to other intracellular membranes.
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Sphingolipidosis 6 trials · 166 incl. sub-types Sub-types →
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Cerebral lipidosis with dementia 0 trials · 38 incl. sub-types Sub-types →
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Neuronal ceroid lipofuscinosis 6 trials · 23 incl. sub-types Sub-types →
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Xanthomatosis 2 trials · 8 incl. sub-types Sub-types →
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Lysosomal acid lipase deficiency 4 trials · 6 incl. sub-types Sub-types →
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Neutral lipid storage disease 1 trial · 2 incl. sub-types Sub-types →
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Triglyceride storage disease 0 trials Sub-types →