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DOID:700 - mitochondrial metabolism disease
Disease Ontology Definition:An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.
Synonyms:
Echinobase Genes : sdhd, nfu1, ttc19, agk, coq2, ears2, bcs1l, gfm1, sucla2, cox10, uqcrc2, atpaf2, cox15, mrps22, sco1,
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
inherited metabolic disorder (is_a)