Biological Sciences and Healthcare, part 1

... > 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 > Isolated long chain hydroxyacyl-CoA dehydrogenase 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 > Isolated long chain hydroxyacyl-CoA dehydrogenase 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 > Isolated long chain hydroxyacyl-CoA dehydrogenase 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 > Isolated long chain hydroxyacyl-CoA dehydrogenase 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 > Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency