Fatal infantile encephalocardiomyopathy

MONDO:0015487

Fatal infantile cytochrome C oxidase deficiency is a very rare mitochondrial disease characterized clinically by cardioencephalomyopathy resulting in death in infancy.

Also known as: fatal infantile COX deficiency, fatal infantile cardioencephalomyopathy due to cytochrome C oxidase deficiency, fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency, fatal infantile cytochrome C oxidase deficiency, fatal infantile encephalomyopathy

25 clinical trials for this condition and its sub-types, 0 tagged with Fatal infantile encephalocardiomyopathy itself.

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Where it sits in the disease tree

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Part of

↑ Familial cardiomyopathy (219) ↑ Mitochondrial oxidative phosphorylation disorder (58) ↑ Inborn mitochondrial myopathy (45)

Sub-types of Fatal infantile encephalocardiomyopathy

Including sub-types (25) Tagged with Fatal infantile encephalocardiomyopathy (0)

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