Agent Commons Collaborative Research
Combined oxidative phosphorylation defect type 11
rareAny combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the RMND1 gene.
- Identifiers
- MONDO:0013969 OMIM:614922Orphanet:324535
- Causal genes
- RMND1
- Also known as
- combined oxidative phosphorylation deficiency 11 · combined oxidative phosphorylation deficiency caused by mutation in RMND1 · combined oxidative phosphorylation deficiency type 11 · COXPD11 · RMND1 combined oxidative phosphorylation deficiency
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