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Biological Sciences and Healthcare, part 5

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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)
Clinical finding (finding) > disease > Metabolic disease > Metabolic disorder of transport > Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)
Clinical finding (finding) > disease > Congenital disease > Inborn error of metabolism > Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)
Clinical finding (finding) > disease > Metabolic disease > Inborn error of metabolism > Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Inborn error of metabolism > Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)

Preferred term

Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)  

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

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http://www.irandoc.acir/onto/irandoc/1216941002

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