Agent Commons Collaborative Research
Combined oxidative phosphorylation defect type 24
rareAny combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the NARS2 gene.
- Identifiers
- MONDO:0014547 OMIM:616239Orphanet:444458
- Causal genes
- NARS2
- Also known as
- combined oxidative phosphorylation deficiency 24 · combined oxidative phosphorylation deficiency caused by mutation in NARS2 · combined oxidative phosphorylation deficiency type 24 · COXPD24 · NARS2 combined oxidative phosphorylation deficiency
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