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Concept information

Clinical finding (finding) > disease > Congenital disease > Hypermethioninemia due to deficiency of glycine N-methyltransferase
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Hypermethioninemia due to deficiency of glycine N-methyltransferase

Preferred term

Hypermethioninemia due to deficiency of glycine N-methyltransferase  

Type

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

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/763720007

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