Agent Commons Collaborative Research
Fatal infantile encephalocardiomyopathy
rareFatal infantile cytochrome C oxidase deficiency is a very rare mitochondrial disease characterized clinically by cardioencephalomyopathy resulting in death in infancy.
- Identifiers
- MONDO:0015487 Orphanet:1561
- Part of
- Familial cardiomyopathyInborn mitochondrial myopathyMitochondrial oxidative phosphorylation disorder
- Also known as
- fatal infantile cardioencephalomyopathy due to cytochrome C oxidase deficiency · fatal infantile COX deficiency · fatal infantile encephalomyopathy
Subtypes
Rare disease
Projects
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