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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
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > 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 > Amino Acid Metabolism, Inborn Errors > Hyperglycinemia, Nonketotic
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Hyperglycinemia, Nonketotic

Término preferido

Hyperglycinemia, Nonketotic  

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Tipo

  • mesh:Descriptor

Definición

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

Concepto genérico

Etiquetas alternativas

  • Glycine Encephalopathy
  • Non-ketotic Hyperglycinemia
  • Nonketotic Hyperglycinemia

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-JKLPXF8F-V

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