Combined oxidative phosphorylation deficiency 29

MONDO:0014781

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the TXN2 gene.

Also known as: COXPD29, TXN2 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency 29, combined oxidative phosphorylation deficiency 29; COXPD29, combined oxidative phosphorylation deficiency caused by mutation in TXN2, combined oxidative phosphorylation deficiency type 29

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation deficiency 29 itself.

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↑ Autosomal recessive disease (999) ↑ Inherited neurodegenerative disorder (808) ↑ Combined oxidative phosphorylation deficiency (0)

Including sub-types (13) Tagged with Combined oxidative phosphorylation deficiency 29 (0)

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