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Summary Literature (0)
MIM:618838 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41; COXPD41

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0030007 - combined oxidative phosphorylation deficiency 41

Disease Ontology (DO):
DOID:0112119 - combined oxidative phosphorylation deficiency 41