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DOID:0060536 - mitochondrial complex I deficiency
Disease Ontology Definition:A mitochondrial metabolism disease characterized by a wide range of manifestations including marked and often fatal lactic acidosis, cardiomyopathy, leukoencephalopathy, pure myopathy and hepatopathy with tubulopathy. Among the numerous clinical phenotypes observed are Leigh syndrome, Leber hereditary optic neuropathy and MELAS syndrome. It can have material basis in mutations in multiple different genes, both nuclear-encoded and mitochondrial-encoded.
Synonyms: isolated NADH-CoQ reductase deficiency, isolated NADH-coenzyme Q reductase deficiency, isolated NADH-ubiquinone reductase deficiency, isolated mitochondrial respiratory chain complex I deficiency,
Xenbase Genes
:
ndufv1,
ndufs8,
ndufs4,
ndufb9,
ndufs1,
ndufv2,
nubpl,
ndufb3,
ndufs2,
ndufaf5,
ndufs3,
ndufaf3,
ndufa6,
ndufa11,
ndufaf1,
| MONDO:0009640 - obsolete mitochondrial complex I deficiency, nuclear type |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
mitochondrial metabolism disease (is_a)