| E75 |
Disorders of sphingolipid metabolism and other lipid storage disorders |
| 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 |
| E75.29 |
Other sphingolipidosis |
| E75.3 |
Sphingolipidosis, unspecified |
| E75.4 |
Neuronal ceroid lipofuscinosis |
| E75.5 |
Other lipid storage disorders |
| E75.6 |
Lipid storage disorder, unspecified |
