Please sign in to follow a disease.

Combined oxidative phosphorylation defect type 24

MONDO:0014547

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the NARS2 gene.

Also known as: COXPD24, NARS2 combined oxidative phosphorylation deficiency, combined oxidative phosphorylation deficiency caused by mutation in NARS2, combined oxidative phosphorylation deficiency type 24, combined oxidative phosphorylation deficiency 24

13 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation defect type 24 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Combined oxidative phosphorylation deficiency (0)

Including sub-types (13) Tagged with Combined oxidative phosphorylation defect type 24 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.