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Concept information

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

Preferred term

hyperornithinemia hyperammonemia homocitrullinuria  

Broader concept

Related concepts

Synonym(s)

  • HHH syndrome
  • hyperornithinemia-hyperammonemia-homocitrullinemia syndrome
  • triple H syndrome

In other languages

URI

http://data.loterre.fr/ark:/67375/BL8-K1R6R4QB-5

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