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DOID:0112100 - mitochondrial type mitochondrial complex I deficiency
Disease Ontology Definition:A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the mitochondrial genome.
Synonyms: MC1DM,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
mitochondrial complex I deficiency (is_a)