Combined Oxidative Phosphorylation Defect Type 8 C4518839
A rare genetic disorder impairing cellular energy production, often affecting muscles, brain, and other organs. Treatment aims to manage symptoms and support affected body systems.
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