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E75.240 Niemann-Pick disease type A
BackE75Disorders of sphingolipid metabolism and other lipid storage disordersCategory7 →E75.0GM2 gangliosidosisCategory4 →E75.00GM2 gangliosidosis, unspecifiedCategoryE75.01Sandhoff diseaseCategoryE75.02Tay-Sachs diseaseCategoryE75.09Other GM2 gangliosidosisCategoryE75.1Other and unspecified gangliosidosisCategory3 →E75.10Unspecified gangliosidosisCategoryE75.11Mucolipidosis IVCategoryE75.19Other gangliosidosisCategoryE75.2Other sphingolipidosisCategory9 →E75.21Fabry (-Anderson) diseaseCategoryE75.22Gaucher diseaseCategoryE75.23Krabbe diseaseCategoryE75.24Niemann-Pick diseaseCategory7 →E75.240Niemann-Pick disease type ACategoryE75.241Niemann-Pick disease type BCategoryE75.242Niemann-Pick disease type CCategoryE75.243Niemann-Pick disease type DCategoryE75.244Niemann-Pick disease type A/BCategoryE75.248Other Niemann-Pick diseaseCategoryE75.249Niemann-Pick disease, unspecifiedCategoryE75.25Metachromatic leukodystrophyCategoryE75.26Sulfatase deficiencyCategoryE75.27Pelizaeus-Merzbacher diseaseCategoryE75.28Canavan diseaseCategoryE75.29Other sphingolipidosisCategoryE75.3Sphingolipidosis, unspecifiedCategoryE75.4Neuronal ceroid lipofuscinosisCategoryE75.5Other lipid storage disordersCategoryE75.6Lipid storage disorder, unspecifiedCategory
CategoryCODABLE
E75.240
Niemann-Pick disease type A
EXAMPLES
Acid sphingomyelinase deficiency type A (ASMD type A)
Infantile neurovisceral acid sphingomyelinase deficiency
Infantile neurovisceral acid sphingomyelinase deficiency
- Chapter
- IV · Endocrine, nutritional and metabolic diseases
- Section
- E70-E88
- Valid from
Source
CMS ICD-10-CM Tabular List, edition FY2026.