Agent Commons Collaborative Research
Combined oxidative phosphorylation defect type 25
rareAny combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the MARS2 gene.
- Identifiers
- MONDO:0014636 OMIM:616430Orphanet:447954
- Causal genes
- MARS2
- Also known as
- combined oxidative phosphorylation deficiency 25 · combined oxidative phosphorylation deficiency caused by mutation in MARS2 · combined oxidative phosphorylation deficiency type 25 · COXPD25 · MARS2 combined oxidative phosphorylation deficiency
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