Sphingolipidoses

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Sphingolipidoses Classification and external resources
ICD-10	E75.3
ICD-9	272.7
DiseasesDB	33438
MeSH	D013106

Sphingolipidoses are a class of disorders relating to Sphingolipid metabolism.

Examples include:

• Fabry's disease
• Gangliosidosis
  • GM1 gangliosidoses
  • GM2 gangliosidoses
    • Tay-Sachs disease
    • Sandhoff disease
• Gaucher's disease
• Krabbe disease
• Metachromatic leukodystrophy
• Niemann-Pick disease

[edit] See also

• Lipid storage disorder

[edit] External links

• MeSH Sphingolipidoses
• -382402491 at GPnotebook

v • d • e Inborn error of lipid metabolism - Lysosomal storage diseases - lipid storage disorders (E75, 272.7-272.8, 330.0-330.1) Sphingolipidoses Gangliosidoses: GM1 gangliosidoses, GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease, AB variant) Fabry's disease - Gaucher's disease sulfated: Leukodystrophy (Metachromatic leukodystrophy, Krabbe disease) ceramide: Farber disease phospholipid: Niemann-Pick disease Neuronal ceroid lipofuscinosis Infantile - Jansky-Bielschowsky disease - Batten disease Other Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman disease) see also glycolipid metabolism enzymes