Template:Lipid storage disorders: Difference between revisions

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Latest revision as of 19:30, 8 March 2025

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

* Cerebrotendinous xanthomatosis

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