E75.- Disorders of sphingolipid metabolism and other lipid storage disorders

Excludes

  • Mucolipidosis, types I-III (E77.0–E77.1)
  • Refsum’s disease (G60.1)
  • 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
      • E75.29
    Other sphingolipidosis
    • E75.3
    Sphingolipidosis, unspecified
    • E75.4
    Neuronal ceroid lipofuscinosis
    • E75.5
    Other lipid storage disorders
    • E75.6
    Lipid storage disorder, unspecified