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Summary Literature (0)
DOID:0111143 - mitochondrial complex V (ATP synthase) deficiency

Disease Ontology Definition:A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex.


Xenbase Genes : atp5f1a, atpaf2, atp5f1d, tmem70, atp6, atp8

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014471 - mitochondrial proton-transporting ATP synthase complex deficiency

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): mitochondrial metabolism disease (is_a)