E71.5 - Peroxisomal disorders
- Applicable to Peroxisomal disorders
- The 2025 edition of ICD10-CM E71.5 became effective on October 1, 2024.
- This is the American ICD10-CM version of E71.5 - other international versions of ICD10 E71.5 may differ.
- E71.5 is a Non-Billable / Non-Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- E71.5 Code should not be used for billing or reimbursement purposes as there are multiple ICD-10 CM codes below it that contain a greater level of detail.
- E71.5 - Peroxisomal disorders
- E71.5 - Peroxisomal disorders
- 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
Type 1 Excludes
- Schilder's disease (G37.0)
The following codes above E71.5 contain annotation back-references that may be applicable to E71.5:
Chapter: E00-E89 Endocrine, nutritional and metabolic diseases
Section: E70-E88 Metabolic disorders
Category: E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
Non-Billable/Non-Specific Code
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