E75 Disord of sphingolipid metab and oth lipid storage disorders
ICD-10-CM category E75 sits in Chapter 4 (Endocrine, nutritional and metabolic diseases, E00-E89). It contains 26 billable codes for FY2027, effective October 1, 2026 to September 30, 2027. Always code to the most specific code available: a code with more characters that describes the diagnosis more precisely takes priority over a shorter one.
Subcategories
E75.0 GM2 gangliosidosisE75.1 Other and unspecified gangliosidosisE75.2 Other sphingolipidosisE75.24 Niemann-Pick disease
Billable codes in E75
| Code | Description |
|---|---|
E75.00 | GM2 gangliosidosis, unspecified |
E75.01 | Sandhoff disease |
E75.02 | Tay-Sachs disease |
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 |
E75.240 | 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 |
Search within ICD-10-CM for E75 and related codes
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