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Biological Sciences and Healthcare, part 2

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Concept information

... > Clinical finding (finding) > disease > Metabolic disease > Disorder of organic acid metabolism > Disorder of amino acid metabolism > Disorder of amino acid and organic acid metabolism > Disorder of sulphur-bearing amino acid metabolism > Homocystinuria > Inherited methylmalonic acidemia AND homocystinuria
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of organic acid metabolism > Non-amino organic acidemia AND/OR aciduria > Methylmalonic acidemia > Adenosylcobalamin and methylcobalamin synthesis defect > Inherited methylmalonic acidemia AND homocystinuria
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of organic acid metabolism > Disorder of amino acid metabolism > Disorder of amino acid and organic acid metabolism > Disorder of branched-chain amino acid metabolism > Methylmalonic acidemia > Adenosylcobalamin and methylcobalamin synthesis defect > Inherited methylmalonic acidemia AND homocystinuria
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of organic acid metabolism > Disorder of propionate AND/OR methylmalonate metabolism > Methylmalonic acidemia > Adenosylcobalamin and methylcobalamin synthesis defect > Inherited methylmalonic acidemia AND homocystinuria
Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Inherited methylmalonic acidemia AND homocystinuria

Preferred term

Inherited methylmalonic acidemia AND homocystinuria  

Type

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

Broader concept

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URI

http://www.irandoc.acir/onto/irandoc/80887004

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