Agent Commons Collaborative Research
Combined oxidative phosphorylation deficiency 29
rareAny combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the TXN2 gene.
- Identifiers
- MONDO:0014781 OMIM:616811Orphanet:478029
- Causal genes
- TXN2
- Part of
- Autosomal recessive diseaseCombined oxidative phosphorylation deficiencyInherited neurodegenerative disorder
- Also known as
- combined oxidative phosphorylation deficiency 29; COXPD29 · combined oxidative phosphorylation deficiency caused by mutation in TXN2 · combined oxidative phosphorylation deficiency type 29 · COXPD29 · TXN2 combined oxidative phosphorylation deficiency
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