... (MCAD) deficiency is a condition that prevents the body from converting certain fats to energy, particularly during periods without food ...
Medium-chain acyl-coenzyme A dehydrogenase deficiency (MCAD) Classification and external resources; Specialty: endocrinology: ICD-10: E71.311: ICD-9-CM: 277.85: OMIM ...
Medium chain acyl-CoA dehydrogenase (MCAD) deficiency is a rare genetic metabolic disorder characterized by a deficiency of the enzyme medium chain acyl ...
Introduction . Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is a rare genetic condition where a person has problems breaking down fatty acids for energy.
Medium-chain acyl-coenzyme A dehydrogenase (MCAD) deficiency is a disorder of mitochondrial fatty acid β-oxidation. Fatty acid β-oxidation fuels hepatic ...
The natural history of medium-chain acyl CoA dehydrogenase deficiency in the Netherlands: clinical presentation and outcome. J Pediatr. 2006 May. 148(5) ...
Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a condition that prevents the body from converting certain fats to energy, ...
Medium chain acyl dehydrogenase deficiency (MCADD) is a rare inherited disorder┬áwhere your body┬ácannot metabolise (break down) fat properly.┬á
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency; Classification and external resources; ICD-9-CM: 277.85: ... Medium chain acyl dehydrogenase deficiency;
ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN; ACADM Alternative titles; symbols: MEDIUM-CHAIN ACYL-CoA DEHYDROGENASE; MCAD; MCADH: HGNC Approved Gene Symbol: ACADM ...