ICD-10-CM category
E75: Disorders of sphingolipid metabolism and other lipid storage disorders
Codes under E75 (Disorders of sphingolipid metabolism and other lipid storage disorders). A ✓ marks a billable (fully specified) code; category codes without a ✓ are not billable on their own.
| Code | Description | Billable |
|---|---|---|
| E75.0 | GM2 gangliosidosis | — |
| E75.00 | GM2 gangliosidosis, unspecified | ✓ |
| E75.01 | Sandhoff disease | ✓ |
| E75.1 | Other and unspecified gangliosidosis | — |
| E75.02 | Tay-Sachs disease | ✓ |
| E75.2 | Other sphingolipidosis | — |
| E75.3 | Sphingolipidosis, unspecified | ✓ |
| E75.4 | Neuronal ceroid lipofuscinosis | ✓ |
| E75.5 | Other lipid storage disorders | ✓ |
| E75.6 | Lipid storage disorder, unspecified | ✓ |
| E75.09 | Other GM2 gangliosidosis | ✓ |
| E75.10 | Unspecified gangliosidosis | ✓ |
| E75.11 | Mucolipidosis IV | ✓ |
| E75.19 | Other gangliosidosis | ✓ |
| E75.21 | Fabry (-Anderson) disease | ✓ |
| E75.22 | Gaucher disease | ✓ |
| E75.23 | Krabbe disease | ✓ |
| E75.24 | Niemann-Pick disease | — |
| E75.25 | Metachromatic leukodystrophy | ✓ |
| E75.26 | Sulfatase deficiency | ✓ |
| E75.27 | Pelizaeus-Merzbacher disease | ✓ |
| E75.28 | Canavan disease | ✓ |
| E75.29 | Other sphingolipidosis | ✓ |
| 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 | ✓ |
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Informational only, not coding or medical advice. Verify against the official ICD-10-CM (FY2026) and your payer's guidelines.
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