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Mitochondrial Complex Iii Deficiency Nuclear Type 7 C4014408

Published: July 22, 2026Updated: August 27, 2026

A rare inherited condition affecting the mitochondria's energy-producing complexes. Primarily seen in children with variable organ involvement. Treatment centers on supportive measures.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 27, 2026Editorial policy

Key facts at a glance

ICD-10
E88.9
ICD-11
5A00.0
Body system
metabolic
Severity
severe
Chronic
true

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

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Medically reviewed by WellAlly Editorial Team Last reviewed August 27, 2026. · Read our editorial policy