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5C53.2 Disorders of mitochondrial oxidative phosphorylation

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

An inborn error of metabolism in cellular respiration (oxidative phosphorylation) in the mitochondria, where a series of enzymes catalyze the transfer of electrons to molecular oxygen and the generation of energy-storing ATP

code elsewhere

• Neuropathy, ataxia, and retinitis pigmentosa  (8C73.1)

sections/codes in this section (5C53.2-5C53.2)

• Mitochondrial DNA depletion syndromes  (5C53.20)
• Multiple mitochondrial DNA deletion syndromes  (5C53.21)
• Coenzyme Q10 deficiency  (5C53.22)
• Mitochondrial protein translation defects  (5C53.23)
• Leigh syndrome  (5C53.24)
• Isolated ATP synthase deficiency  (5C53.25)
• Other specified disorders of mitochondrial oxidative phosphorylation  (5C53.2Y)
• Disorders of mitochondrial oxidative phosphorylation, unspecified  (5C53.2Z)

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