1.01.f

Disorders of glycine and serine metabolism

  • Nonketotic hyperglycinemia due to glycine decarboxylase deficiency (Glycine encephalopathy)
  • Nonketotic hyperglycinemia due to aminomethyltransferase deficiency (Glycine encephalopathy)
  • 3-phosphoglycerate dehydrogenase deficiency
  • Phosphoserine aminotransferase deficiency
  • Phosphoserine phosphatase deficiency
  • ASCT1 transporter deficiency (Spastic tetraplegia, thin corpus callosum, and progressive microcephaly)
  • Mitochondrial serine hydroxymethyltransferase deficiency

Subnetworks

AOA 1

AOA

Aminoacid and organic acids related disorders

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