Mitochondrial Complex I Deficiency Nuclear Type 13 C4748770
A rare genetic condition where cells cannot produce energy properly due to defects in the first protein complex of the mitochondria. It can affect the brain, muscles, and heart. Care involves supportive treatment and metabolic monitoring.
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 25, 2026. · Read our editorial policy