Fatal infantile cytochrome C oxidase deficiency is a very rare mitochondrial disease characterized clinically by cardioencephalomyopathy resulting in death in infancy.
Comprehensive, easy-to-understand information about this condition
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myopathy, lactic acidosis, and sideroblastic anemia
MONDO:0000863
mitochondrial encephalomyopathy
MONDO:0004675
progressive external ophthalmoplegia
MONDO:0005181
mitochondrial myopathy with a defect in mitochondrial-protein transport
MONDO:0009638
Barth syndrome
MONDO:0010543
mitochondrial myopathy with diabetes
MONDO:0010773