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| リンク元 | 「スフィンゴリピドーシス」 | 
| 関連記事 | 「症」 | 
| Disease | Enzyme Deficiency | Lipid Accumulating | Clinical Symptoms | 
| Tay-Sachs disease | Hexosaminidase A | Cer-Glc-Gal(NeuAc)-: : GalNAc GM2 Ganglioside  | 
Mental retardation, blindness, muscular weakness. | 
| Fabry's disease | α-Galactosidase | Cer-Glc-Gal-: : Gal Globotriaosylceramide  | 
Skin rash, kidney failure (full symptoms only in males; X-linked recessive). | 
| Metachromatic leukodystrophy | Arylsulfatase A | Cer-Gal-: : OSO3 3-Sulfogalactosylceramide  | 
Mental retardation and psychologic disturbances in adults; demyelination. | 
| Krabbe's disease | β-Galactosidase | Cer-: : Gal Galactosylceramide  | 
Mental retardation; myelin almost absent. | 
| Gaucher's disease | β-Glucosidase | Cer-: : Glc Glucosylceramide  | 
Enlarged liver and spleen, erosion of long bones, mental retardation in infants. | 
| Niemann-Pick disease | Sphingomyelinase | Cer-: : P-choline Sphingomyelin  | 
Enlarged liver and spleen, mental retardation; fatal in early life. | 
| Farber's disease | Ceramidase | Acyl-: : Sphingosine Ceramide  | 
Hoarseness, dermatitis, skeletal deformation, mental retardation; fatal in early life. | 
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