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Summary Literature (0)
MIM:610505 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3; COXPD3

Xenbase Genes: tsfm

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012512 - fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3

Disease Ontology (DO):
DOID:0060286 - combined oxidative phosphorylation deficiency
DOID:0111486 - combined oxidative phosphorylation deficiency 3