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36
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Acyl
- Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a condition that prevents the body from converting certain fats into energy, particularly during ...
- Short-chain acyl-CoA dehydrogenase (SCAD) deficiency is a condition that prevents the body from converting certain fats into energy, especially during periods ...
- Peroxisomal acyl-CoA oxidase deficiency is a disorder that causes deterioration of nervous system functions (neurodegeneration) beginning in infancy. Newborns with ...
- Short/branched chain acyl-CoA dehydrogenase (SBCAD) deficiency (also known as 2-methylbutyryl-CoA dehydrogenase deficiency) is a rare disorder in which the body ...
- Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a condition that prevents the body from converting certain fats to energy, particularly ... instructions for making an enzyme called medium-chain acyl-CoA dehydrogenase, which is required to break down ( ...
- ... for making an enzyme called peroxisomal straight-chain acyl-CoA oxidase. This enzyme is found in sac- ...
- ... for making an enzyme called short/branched chain acyl-CoA dehydrogenase (SBCAD, also known as 2-methylbutyryl- ... gene mutations in people with short/branched chain acyl-CoA dehydrogenase (SBCAD) deficiency. While most people with ...
- ... instructions for making an enzyme called short-chain acyl-CoA dehydrogenase (SCAD). This enzyme functions within mitochondria, ... gene have been found to cause short-chain acyl-CoA dehydrogenase (SCAD) deficiency. Almost all of these ...
- ... instructions for making an enzyme called medium-chain acyl-CoA dehydrogenase (MCAD). This enzyme functions within mitochondria, ... gene have been found to cause medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. Many of these mutations ...
- ... unclear. More About This Health Condition ACSF3_HUMAN acyl-CoA synthetase family member 3, mitochondrial acyl-CoA synthetase family member 3, mitochondrial precursor Tests ...
