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Concept information

disease > metabolic diseases > inborn error metabolism > metabolism disorder urea cycle > N-acetylglutamate synthase deficiency
... > artificial nutrition > enteral nutrition > indication for enteral nutrition > at risk of malnutrition and functional gastrointestinal tract > inborn error metabolism > metabolism disorder urea cycle > N-acetylglutamate synthase deficiency
... > patient care management > delivery of health care > nutritional support > enteral nutrition > indication for enteral nutrition > at risk of malnutrition and functional gastrointestinal tract > inborn error metabolism > metabolism disorder urea cycle > N-acetylglutamate synthase deficiency
... > artificial nutrition > enteral nutrition > indication for enteral nutrition for children > inborn error metabolism > metabolism disorder urea cycle > N-acetylglutamate synthase deficiency
... > patient care management > delivery of health care > nutritional support > enteral nutrition > indication for enteral nutrition for children > inborn error metabolism > metabolism disorder urea cycle > N-acetylglutamate synthase deficiency
disease > hereditary disease > inborn error metabolism > metabolism disorder urea cycle > N-acetylglutamate synthase deficiency

Término preferido

N-acetylglutamate synthase deficiency  

Concepto genérico

Etiquetas alternativas

  • hyperammonemia due to N-Acetylglutamate synthetase deficiency
  • N-Acetylglutamate synthetase deficiency

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/BL8-VBKPTTT9-F

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