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Disease Ontology Browser
mitochondrial complex V (ATP synthase) deficiency (DOID:0111143)
Alliance: disease page
Alt IDs: ORDO:254913, UMLS_CUI:C4757950
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory