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Summary Literature (0)
MIM:619024 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 49; COXPD49

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0033569 - combined oxidative phosphorylation deficiency 49

Disease Ontology (DO):
DOID:0112110 - combined oxidative phosphorylation deficiency 49