A mitochondrial energy metabolism disorder where respiratory complex (I–V) is dysfunctional, typically due to mutations in genes encoding that specific complex’s proteins or assembly factors.
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combined oxidative phosphorylation deficiency
MONDO:0000732
myopathy, lactic acidosis, and sideroblastic anemia
MONDO:0000863
optic atrophy 3
MONDO:0008133
autosomal dominant optic atrophy, classic form
MONDO:0008134
Leigh syndrome
MONDO:0009723
mitochondrial non-syndromic sensorineural hearing loss
MONDO:0010779