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Concept information

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

Preferred term

citrullinemia  

Broader concept

Related concepts

Entry terms

  • argininosuccinate synthase deficiency disease
  • argininosuccinate synthetase deficiencies
  • argininosuccinic acid synthase deficiency disease
  • argininosuccinic acid synthetase deficiency
  • argininosuccinic acid synthetase deficiency disease

In other languages

  • citrullinémie

    French

  • déficit en argininosuccinate synthase
  • déficit en argininosuccinate synthétase
  • déficit enzymatique complet en argininosuccinate synthase

URI

http://data.loterre.fr/ark:/67375/BL8-T5J5VKST-F

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