Disorders of sphingolipid metabolism and other lipid storage disorders - E75

 Type 1 Excludes

• mucolipidosis, types I-III (E77.0-E77.1)
• Refsum's disease (G60.1)

 Codes

• E75.0 - GM2 gangliosidosis
• E75.00 - GM2 gangliosidosis, unspecified
• E75.01 - Sandhoff disease
• E75.02 - Tay-Sachs disease
• E75.09 - Other GM2 gangliosidosis
• E75.1 - Other and unspecified gangliosidosis
• E75.10 - Unspecified gangliosidosis
• E75.11 - Mucolipidosis IV
• E75.19 - Other gangliosidosis
• E75.2 - Other sphingolipidosis
• E75.21 - Fabry (-Anderson) disease
• E75.22 - Gaucher disease
• E75.23 - Krabbe disease
• E75.24 - Niemann-Pick disease
• E75.240 - Niemann-Pick disease type A
• E75.241 - Niemann-Pick disease type B
• E75.242 - Niemann-Pick disease type C
• E75.243 - Niemann-Pick disease type D
• E75.244 - Niemann-Pick disease type A/B
• E75.248 - Other Niemann-Pick disease
• E75.249 - Niemann-Pick disease, unspecified
• E75.25 - Metachromatic leukodystrophy
• E75.26 - Sulfatase deficiency
• E75.27 - Pelizaeus-Merzbacher disease
• E75.28 - Canavan disease
• E75.29 - Other sphingolipidosis
• E75.3 - Sphingolipidosis, unspecified
• E75.4 - Neuronal ceroid lipofuscinosis
• E75.5 - Other lipid storage disorders
• E75.6 - Lipid storage disorder, unspecified