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disease > metabolic diseases > inborn error metabolism > metabolism disorder urea cycle > carbamoyl-phosphate synthase 1 deficiency
... > artificial nutrition > enteral nutrition > indication for enteral nutrition > at risk of malnutrition and functional gastrointestinal tract > inborn error metabolism > metabolism disorder urea cycle > carbamoyl-phosphate synthase 1 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 > carbamoyl-phosphate synthase 1 deficiency
... > artificial nutrition > enteral nutrition > indication for enteral nutrition for children > inborn error metabolism > metabolism disorder urea cycle > carbamoyl-phosphate synthase 1 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 > carbamoyl-phosphate synthase 1 deficiency
disease > hereditary disease > inborn error metabolism > metabolism disorder urea cycle > carbamoyl-phosphate synthase 1 deficiency

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carbamoyl-phosphate synthase 1 deficiency  

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http://data.loterre.fr/ark:/67375/BL8-CM2X9D72-M

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