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Disease Ontology Browser
mitochondrial complex V (ATP synthase) deficiency nuclear type 3 (DOID:0060332)
Synonyms: MC5DN3
Alt IDs: OMIM:614053, ICD10CM:E88.8, ORDO:254913
Definition: A mitochondrial metabolism disease that has material basis in mutation in the ATP5E gene on chromosome 20q13.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory