ICD-10-CM category
E75 Disorders of sphingolipid metabolism and other lipid storage disorders
E75 is a category, not a billable code. Report one of the 26 complete codes below.
Codes in E75
- E75.00GM2 gangliosidosis, unspecified
- E75.01Sandhoff disease
- E75.02Tay-Sachs disease
- E75.09Other GM2 gangliosidosis
- E75.10Unspecified gangliosidosis
- E75.11Mucolipidosis IV
- E75.19Other gangliosidosis
- E75.21Fabry (-Anderson) disease
- E75.22Gaucher disease
- E75.23Krabbe disease
- E75.240Niemann-Pick disease type A
- E75.241Niemann-Pick disease type B
- E75.242Niemann-Pick disease type C
- E75.243Niemann-Pick disease type D
- E75.244Niemann-Pick disease type A/B
- E75.248Other Niemann-Pick disease
- E75.249Niemann-Pick disease, unspecified
- E75.25Metachromatic leukodystrophy
- E75.26Sulfatase deficiency
- E75.27Pelizaeus-Merzbacher disease
- E75.28Canavan disease
- E75.29Other sphingolipidosis
- E75.3Sphingolipidosis, unspecified
- E75.4Neuronal ceroid lipofuscinosis
- E75.5Other lipid storage disorders
- E75.6Lipid storage disorder, unspecified
Outside the US? E75 in the international WHO ICD-10 lists its inclusion and exclusion notes.
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ICD-10-CM is developed by the National Center for Health Statistics (NCHS), Centers for Disease Control and Prevention, U.S. Department of Health and Human Services, and is based on the WHO ICD-10. Codes and titles are reproduced unchanged from the FY2026 code list (effective 1 October 2025). Their use here does not imply endorsement by CDC, HHS or the U.S. Government. Changes effective on or after 1 October 2026 may not be reflected yet; check the current release at cdc.gov or cms.gov before submitting claims.
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