Index to Diseases and Injuries
Disorder › peroxisomal
Index code:E71.50
- biogenesis
- neonatal adrenoleukodystrophy E71.511
- specified disorder NEC E71.518
- Zellweger syndrome E71.510
- rhizomelic chondrodysplasia punctata E71.540
- specified form NEC E71.548
- group 1 E71.518
- group 2 E71.53
- group 3 E71.542
- X-linked adrenoleukodystrophy E71.529
- adolescent E71.521
- adrenomyeloneuropathy E71.522
- childhood E71.520
- specified form NEC E71.528
- Zellweger-like syndrome E71.541
Use the index to find a code, then confirm it in the Tabular List before assigning it. A code ending in a dash is incomplete, and a code in [brackets] is a manifestation code reported after the underlying condition. Search the whole index.
Frequently asked questions
What is the ICD-10-CM code for Disorder › peroxisomal?
The ICD-10-CM Alphabetic Index directs "Disorder › peroxisomal" to E71.50. Subterms below it may lead to a more specific code. Always confirm the code in the Tabular List before assigning it.
ICD-10-CM Index to Diseases and Injuries maintained by CDC/NCHS (public domain), from the CMS FY2027 release.