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Up to: Mitochondrial oxidative phosphorylation disorder

Mitochondrial respiratory chain complex deficiency

A mitochondrial energy metabolism disorder where respiratory complex (I–V) is dysfunctional, typically due to mutations in genes encoding that specific complex’s proteins or assembly factors.

4 trials tagged with this condition →

  • Mitochondrial complex I deficiency 2 trials Sub-types →
  • Mitochondrial complex IV deficiency, nuclear-type 1 trial Sub-types →
  • SDHC-related Mitochondrial Disease 0 trials
  • Mitochondrial complex III deficiency 0 trials Sub-types →
  • Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1 0 trials
  • Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2 0 trials
  • Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 0 trials
  • Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B 0 trials
  • Mitochondrial complex V (ATP synthase) deficiency, nuclear type 5 0 trials

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