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Combined oxidative phosphorylation deficiency

MONDO:0000732

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

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation deficiency itself.

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Part of

↑ Mitochondrial oxidative phosphorylation disorder (58)

Sub-types of Combined oxidative phosphorylation deficiency

Combined oxidative phosphorylation defect type 11 0 trials
Combined oxidative phosphorylation defect type 13 0 trials
Combined oxidative phosphorylation defect type 14 0 trials
Combined oxidative phosphorylation defect type 15 0 trials
Combined oxidative phosphorylation defect type 17 0 trials
Combined oxidative phosphorylation defect type 2 0 trials
Combined oxidative phosphorylation defect type 20 0 trials
Combined oxidative phosphorylation defect type 21 0 trials
Combined oxidative phosphorylation defect type 23 0 trials
Combined oxidative phosphorylation defect type 24 0 trials
Combined oxidative phosphorylation defect type 25 0 trials
Combined oxidative phosphorylation defect type 26 0 trials
Combined oxidative phosphorylation defect type 27 0 trials
Combined oxidative phosphorylation defect type 30 0 trials
Combined oxidative phosphorylation defect type 4 0 trials
Combined oxidative phosphorylation defect type 7 0 trials
Combined oxidative phosphorylation defect type 8 0 trials
Combined oxidative phosphorylation defect type 9 0 trials
Combined oxidative phosphorylation deficiency 19 0 trials
Combined oxidative phosphorylation deficiency 28 0 trials
Combined oxidative phosphorylation deficiency 29 0 trials
Combined oxidative phosphorylation deficiency 32 0 trials
Combined oxidative phosphorylation deficiency 33 0 trials
Combined oxidative phosphorylation deficiency 34 0 trials
Combined oxidative phosphorylation deficiency 35 0 trials
Combined oxidative phosphorylation deficiency 36 0 trials
Combined oxidative phosphorylation deficiency 37 0 trials
Combined oxidative phosphorylation deficiency 38 0 trials
Combined oxidative phosphorylation deficiency 39 0 trials
Combined oxidative phosphorylation deficiency 40 0 trials
Combined oxidative phosphorylation deficiency 41 0 trials
Combined oxidative phosphorylation deficiency 42 0 trials
Combined oxidative phosphorylation deficiency 43 0 trials
Combined oxidative phosphorylation deficiency 44 0 trials
Combined oxidative phosphorylation deficiency 45 0 trials
Combined oxidative phosphorylation deficiency 46 0 trials
Combined oxidative phosphorylation deficiency 47 0 trials
Combined oxidative phosphorylation deficiency 48 0 trials
Combined oxidative phosphorylation deficiency 51 0 trials
Combined oxidative phosphorylation deficiency 52 0 trials
Combined oxidative phosphorylation deficiency 53 0 trials
Combined oxidative phosphorylation deficiency 54 0 trials
Combined oxidative phosphorylation deficiency 55 0 trials
Combined oxidative phosphorylation deficiency 56 0 trials
Combined oxidative phosphorylation deficiency 57 0 trials
Combined oxidative phosphorylation deficiency 58 0 trials
Combined oxidative phosphorylation deficiency 59 0 trials
Combined oxidative phosphorylation deficiency 60 0 trials
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
8 sub-types
Severe X-linked mitochondrial encephalomyopathy 0 trials

Including sub-types (13) Tagged with Combined oxidative phosphorylation deficiency (0)

Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 4 Completed 2 Terminated 1

New DNA test could end years of uncertainty for mitochondrial disease patients

Diagnosis Not yet recruiting

This pilot study aims to develop a new digital PCR technique to more accurately diagnose mitochondrial diseases. Researchers will test the method on blood, urine, saliva, and muscle fiber samples from 4 patients. If validated, the technique could be faster and cheaper than curren…

Sponsor: Centre Hospitalier Universitaire de Nice • Aim: Diagnosis

Last updated Jun 27, 2026 12:04 UTC