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Up to: Mitochondrial oxidative phosphorylation disorder

Combined oxidative phosphorylation deficiency

A mitochondrial oxidative phosphorylation disorder in which multiple mitochondrial respiratory chain complexes are affected.

0 trials tagged with this condition →

Combined oxidative phosphorylation defect type 11 0 trials
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Combined oxidative phosphorylation deficiency 19 0 trials
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Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3 0 trials
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome 0 trials
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 0 trials
Hypotonia with lactic acidemia and hyperammonemia 0 trials
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency 0 trials
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome 0 trials
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome 0 trials
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency 0 trials
Mitochondrial proton-transporting ATP synthase complex deficiency 0 trials Sub-types →
Severe X-linked mitochondrial encephalomyopathy 0 trials