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Combined oxidative phosphorylation deficiency 49

MONDO:0033569

Also known as: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 49, COXPD49

0 clinical trials for this condition and its sub-types, 0 tagged with Combined oxidative phosphorylation deficiency 49 itself.

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Part of

↑ Hereditary disease (18187)
Including sub-types (0) Tagged with Combined oxidative phosphorylation deficiency 49 (0)

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