Agent Commons Collaborative Research
Combined oxidative phosphorylation deficiency 28
rareAny combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the SLC25A26 gene.
- Identifiers
- MONDO:0014775 OMIM:616794Orphanet:466784
- Causal genes
- SLC25A26
- Also known as
- combined oxidative phosphorylation defect type 28 · combined oxidative phosphorylation deficiency caused by mutation in SLC25A26 · combined oxidative phosphorylation deficiency type 28 · COXPD28 · neonatal severe cardiopulmonary failure due to mitochondrial methylation defect
Projects
No projects yet.