ICD-10-CM › E00-E89 › E70-E88 › E75.2 Other sphingolipidosis › E75.27
E75.27
Pelizaeus-Merzbacher disease
ValidICD-10-CM diagnosis code.
Valid for claims with a date of service in the current code year.
What has happened to this code
Every change the publisher made, from 2024 to now.
- FY2024 Added to the code set Pelizaeus-Merzbacher disease
Official coding rules
Published by CDC for FY2027. A rule attached to a category binds every code beneath it, so the rules inherited from this code's ancestors are shown with the code they come from.
Inherited from E75 Disorders of sphingolipid metabolism and other lipid storage disorders
Excludes1 - never coded here
- mucolipidosis, types I-III (E77.0-E77.1)
- Refsum's disease (G60.1)
Inherited from the E70-E88 section Metabolic disorders (E70-E88)
Excludes1 - never coded here
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
Excludes2 - not included here
- Ehlers-Danlos syndromes (Q79.6-)
How CDC's index refers to this code
Wording from the official alphabetic index. Much of it appears nowhere in the code description, which is why a search for the everyday phrase so often finds nothing.
- Merzbacher-Pelizaeus disease
- Pelizaeus-Merzbacher disease
- Aplasia > Pelizaeus-Merzbacher
Codes in the same group
| Code | Description | Status |
|---|---|---|
| E75.21 | Fabry (-Anderson) disease | Valid |
| E75.22 | Gaucher disease | Valid |
| E75.23 | Krabbe disease | Valid |
| E75.24 | Niemann-Pick disease | Not billable |
| E75.25 | Metachromatic leukodystrophy | Valid |
| E75.26 | Sulfatase deficiency | Valid |
| E75.28 | Canavan disease | Valid |
| E75.29 | Other sphingolipidosis | Valid |