Template:Lipid storage disorders

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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