combined oxidative phosphorylation deficiency
MONDO:0000732Mondo
Findings
No curated finding names combined oxidative phosphorylation deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A mitochondrial oxidative phosphorylation disorder in which multiple mitochondrial respiratory chain complexes are affected.
Definition from the Mondo Disease Ontology (MONDO:0000732), read 2026-09-29. CC BY 4.0.
Genes
2 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
- Narrower terms (58)
- combined oxidative phosphorylation defect type 11
- combined oxidative phosphorylation defect type 13
- combined oxidative phosphorylation defect type 14
- combined oxidative phosphorylation defect type 15
- combined oxidative phosphorylation defect type 17
- combined oxidative phosphorylation defect type 2
- combined oxidative phosphorylation defect type 20
- combined oxidative phosphorylation defect type 21
- combined oxidative phosphorylation defect type 23
- combined oxidative phosphorylation defect type 24
- combined oxidative phosphorylation defect type 25
- combined oxidative phosphorylation defect type 26
- combined oxidative phosphorylation defect type 27
- combined oxidative phosphorylation defect type 30
- combined oxidative phosphorylation defect type 4
- combined oxidative phosphorylation defect type 7