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Template
:
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
NCL
Infantile
Jansky–Bielschowsky disease
Batten disease
Other
Cerebrotendinous xanthomatosis
Cholesteryl ester storage disease
(
Lysosomal acid lipase deficiency
/
Wolman disease
)
Sea-blue histiocytosis
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