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Summary Literature (1)
MIM:617713 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33

Xenbase Genes: c1qbp

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054677 - combined oxidative phosphorylation deficiency 33

Disease Ontology (DO):
DOID:0111495 - combined oxidative phosphorylation deficiency 33