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Category:Lipid storage disorders

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Lysosomal storage diseases: Inborn errors of lipid metabolism (Lipid storage disorders)

Sphingolipidoses
(to ceramide)

From ganglioside (gangliosidoses)	Ganglioside: GM1 gangliosidoses GM2 gangliosidoses (Sandhoff disease Tay–Sachs disease AB variant)
From globoside	Globotriaosylceramide: Fabry's disease
From sphingomyelin	Sphingomyelin: phospholipid: Niemann–Pick disease (SMPD1-associated type C) Glucocerebroside: Gaucher's disease
From sulfatide (sulfatidoses leukodystrophy)	Sulfatide: Metachromatic leukodystrophy Multiple sulfatase deficiency Galactocerebroside: Krabbe disease
To sphingosine	Ceramide: Farber disease

Other

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Subcategories

This category has only the following subcategory.

T

Tay–Sachs disease (4 P)

Pages in category "Lipid storage disorders"

The following 31 pages are in this category, out of 31 total. This list may not reflect recent changes.

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