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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)
Clinical finding (finding) > disease > Metabolic disease > Neonatal metabolic disorder (disorder) > Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)
... > Clinical finding (finding) > disease > Disorder of fetus or newborn (disorder) > Neonatal disease > Neonatal metabolic disorder (disorder) > Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)
Clinical finding (finding) > Newborn finding > Neonatal disease > Neonatal metabolic disorder (disorder) > Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)
... > Clinical finding (finding) > disease > Metabolic disease > Enzymopathy > Acyl-CoA dehydrogenase deficiency > Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)

Preferred term

Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)  

Type

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

Clinical course

URI

http://www.irandoc.acir/onto/irandoc/723552005

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