Other sphingolipidosis
Non-billable header
E75.2 is a non-billable header code. Use one of the more specific codes below.
Inclusion terms
Includes (from E75)
- Note: All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
Excludes1
Not coded here — never report together with this code.
- adrenoleukodystrophy [Addison-Schilder] (E71.528)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74) (from E75)
- androgen insensitivity syndrome (E34.5-) (from E75)
- congenital adrenal hyperplasia (E25.0) (from E75)
- hemolytic anemias attributable to enzyme disorders (D55.-) (from E75)
- Marfan syndrome (Q87.4-) (from E75)
- 5-alpha-reductase deficiency (E29.1) (from E75)
- mucolipidosis, types I-III (E77.0-E77.1) (from E75)
- Refsum's disease (G60.1) (from E75)
Excludes2
Not included here — may be reported together when both conditions exist.
Parent code
- E75Disorders of sphingolipid metabolism and other lipid storage disordersHeader
More specific codes E75.2
- E75.21Fabry (-Anderson) diseaseBillable
- E75.22Gaucher diseaseBillable
- E75.23Krabbe diseaseBillable
- E75.24Niemann-Pick diseaseHeader
- E75.25Metachromatic leukodystrophyBillable
- E75.26Sulfatase deficiencyBillable
- E75.27Pelizaeus-Merzbacher diseaseBillable
- E75.28Canavan diseaseBillable
- E75.29Other sphingolipidosisBillable