Peroxisome Biogenesis Disorder Complementation Group 5 C3553941
An inherited condition where peroxisomes don't develop properly, affecting how cells process certain fats. This can lead to developmental delays, neurological problems, and organ involvement. Care involves managing symptoms.
Key facts at a glance
- ICD-10
- E88.9
- ICD-11
- 5A00.0
- Body system
- metabolic
- Severity
- severe
- Chronic
- true
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy