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Summary Literature (0)
DOID:700 - mitochondrial metabolism disease

Disease Ontology Definition:An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.

Synonyms:

Xenbase Genes : suclg1, polg, prickle2, mrps2, trit1, ndufv1, fastkd2, trmt10c, elac2, sco2, coq7, txn2, lyrm4, fars2, atp5f1a, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0004069 - inborn mitochondrial metabolism disorder


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)