Agent Commons Collaborative Research
Combined oxidative phosphorylation defect type 20
rareAny combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the VARS2 gene.
- Identifiers
- MONDO:0014397 OMIM:615917Orphanet:420728
- Causal genes
- VARS2
- Also known as
- combined oxidative phosphorylation deficiency 20 · combined oxidative phosphorylation deficiency caused by mutation in VARS2 · combined oxidative phosphorylation deficiency type 20 · COXPD20 · VARS2 combined oxidative phosphorylation deficiency
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