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DOID:0060286 - combined oxidative phosphorylation deficiency
Disease Ontology Definition:n_a
Synonyms:
Echinobase Genes : ears2, gfm1, mrps22, mrpl44, tufm, rmnd1, pnpt1, tsfm, mrpl3, fars2, mrps16
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
mitochondrial metabolism disease (is_a)