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Summary Literature (0)
DOID:0080118 - mitochondrial complex III deficiency nuclear type 9


Disease Ontology Definition:A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC3 gene on chromosome 11q12.

Synonyms:

Xenbase Genes : uqcc3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014496 - mitochondrial complex III deficiency nuclear type 9


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): genetic disease (is_a), mitochondrial complex III deficiency (is_a)