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Summary Literature (0)
MIM:618120 - MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5

Xenbase Genes: atp5f1d

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0020858 - mitochondrial complex 5 (ATP synthase) deficiency nuclear type 5

Disease Ontology (DO):
DOID:0070463 - mitochondrial complex V (ATP synthase) deficiency nuclear type 5