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Biological Sciences and Healthcare, part 1

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Concept information

... > Clinical finding (finding) > disease > Metabolic disease > Disorder of organic acid metabolism > Disorder of fatty acid metabolism > Fatty acid oxidation defect (disorder) > Mitochondrial trifunctional protein deficiency > 3-Ketoacyl-CoA triolase deficiency
... > Clinical finding (finding) > disease > Metabolic disease > Inborn error of metabolism > Disorder of fatty acid metabolism > Fatty acid oxidation defect (disorder) > Mitochondrial trifunctional protein deficiency > 3-Ketoacyl-CoA triolase deficiency
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Inborn error of metabolism > Disorder of fatty acid metabolism > Fatty acid oxidation defect (disorder) > Mitochondrial trifunctional protein deficiency > 3-Ketoacyl-CoA triolase deficiency
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of lipoprotein AND/OR lipid metabolism > Disorder of fatty acid metabolism > Fatty acid oxidation defect (disorder) > Mitochondrial trifunctional protein deficiency > 3-Ketoacyl-CoA triolase deficiency
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Fatty acid oxidation defect (disorder) > Mitochondrial trifunctional protein deficiency > 3-Ketoacyl-CoA triolase deficiency

Preferred term

3-Ketoacyl-CoA triolase deficiency  

Type

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

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URI

http://www.irandoc.acir/onto/irandoc/307130006

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