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Combined oxidative phosphorylation deficiency 50

MONDO:0033570

Also known as: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 50, COXPD50

0 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation deficiency 50 itself.

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Part of

↑ Hereditary disease (18235)
Including sub-types (0) Tagged with Combined oxidative phosphorylation deficiency 50 (0)

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