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Results 1 - 3 of 3 for Combined oxidative phosphorylation defect type 2
  1. Combined oxidative phosphorylation deficiency 1 
    ... COXPD1 Early fatal progressive hepatoencephalopathy Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Genetic Testing Registry: Hepatoencephalopathy due to combined ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  2. RRM2B gene 
    ... that eye muscles are commonly affected by mitochondrial defects because they are especially ... combined with muscle weakness (encephalomyopathy) and a problem with ...
    https://medlineplus.gov/genetics/gene/rrm2b - Genetics
  3. Primary coenzyme Q10 deficiency 
    ... plays an essential role in a process called oxidative phosphorylation, which converts the energy from food into a ... that a shortage (deficiency) of coenzyme Q10 impairs oxidative phosphorylation and increases the vulnerability of cells to damage ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics