Peroxisome Biogenesis Disorder 11b C3554001
A rare genetic condition where cells cannot form working peroxisomes, leading to buildup of harmful substances. Affected children often experience neurological problems, vision loss, and hearing difficulties. Care involves supportive treatments and monitoring of multiple organs.
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 27, 2026. · Read our editorial policy