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Up to: Familial hypertrophic cardiomyopathy · Disorder of fatty acid oxidation and ketogenesis
Very long chain acyl-CoA dehydrogenase deficiency
An inherited disorder of mitochondrial long-chain fatty acid oxidation with a variable presentation including: cardiomyopathy, hypoketotic hypoglycemia, liver disease, exercise intolerance and rhabdomyolysis.
This condition has no sub-types.