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Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Hyperglycinemia, Nonketotic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Hyperglycinemia, Nonketotic
Nutritional and Metabolic Diseases > Metabolic Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > Hyperglycinemia, Nonketotic
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > Hyperglycinemia, Nonketotic
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > Hyperglycinemia, Nonketotic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > Hyperglycinemia, Nonketotic

Preferred term

Hyperglycinemia, Nonketotic  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Encephalopathies, Glycine
  • Encephalopathy, Glycine
  • Glycine Encephalopathies
  • Glycine Encephalopathy
  • Hyperglycinemia, Non-ketotic
  • Hyperglycinemias, Non-ketotic
  • Non ketotic Hyperglycinemia
  • Non-ketotic Hyperglycinemia
  • Nonketotic Hyperglycinemia
  • Non-ketotic Hyperglycinemias

Note

  • Do not confuse with HYPERGLYCEMIC HYPEROSMOLAR NONKETOTIC COMA

Scope note

  • An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system.

History note

  • 2000

In other languages

URI

http://www.yso.fi/onto/mesh/D020158

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