E71.5 – Peroxisomal disorders
Coding Notes
Active
Non-billable / Non-specific, not valid for HIPAA-covered transactions
Type 1 Excludes
Schilder's disease (G37.0)
Child Codes
Sibling Codes
Parent Sibling Codes
View in Tabular
| Code | Title |
|---|---|
| E00-E89 | Endocrine, nutritional and metabolic diseases (E00-E89) |
| E70-E88 | Metabolic disorders (E70-E88) |
| E71 | Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism |
| E71.5 |
Peroxisomal disorders
Type 1 Excludes
Schilder's disease (G37.0)
|
| E71.50 | Peroxisomal disorder, unspecified |
| E71.51 | Disorders of peroxisome biogenesis |
| E71.510 | Zellweger syndrome |
| E71.511 | Neonatal adrenoleukodystrophy |
| E71.518 | Other disorders of peroxisome biogenesis |
| E71.52 | X-linked adrenoleukodystrophy |
| E71.520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71.521 | Adolescent X-linked adrenoleukodystrophy |
| E71.522 | Adrenomyeloneuropathy |
| E71.528 | Other X-linked adrenoleukodystrophy |
| E71.529 | X-linked adrenoleukodystrophy, unspecified type |
| E71.53 | Other group 2 peroxisomal disorders |
| E71.54 | Other peroxisomal disorders |
| E71.540 | Rhizomelic chondrodysplasia punctata |
| E71.541 | Zellweger-like syndrome |
| E71.542 | Other group 3 peroxisomal disorders |
| E71.548 | Other peroxisomal disorders |