HADHA
Encyclopedia
HADHA is a gene associated with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, often shortened to LCHAD deficiency, is a rare autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats into energy...
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See also
- Mitochondrial trifunctional proteinMitochondrial trifunctional proteinMitochondrial trifunctional protein is a protein which catalyzes several reactions in beta oxidation. It has two subunits:* HADHA* HADHBThe three functions are long-chain 3-hydroxy acyl-coenzyme A dehydrogenase, 2-enoyl coenzyme A hydratase, and long-chain 3-ketoacyl CoA...