Inherited disorder characterised by episodes of metabolic crisis and acute encephalopathy. Life-threatening episodes manifest with poor feeding, vomiting, weight loss, lethargy, tachypnea, seizures or coma and are caused by hyperammonaemia, metabolic

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déficit en CA-VA

SNOMEDCT-BE (disorder) / 764456001

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Inherited disorder characterized by episodes of metabolic crisis and acute encephalopathy. Life-threatening episodes manifest with poor feeding, vomiting, weight loss, lethargy, tachypnea, seizures or coma and are caused by hyperammonemia, metabolic

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encéphalopathie hyperammoniémique par déficit en anhydrase carbonique VA

SNOMEDCT-BE (disorder) / 764456001

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metabolic disorder

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perturbation du métabolisme

médecine

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Disorders of:histidine metabolism | tryptophan metabolism

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Anomalies du métabolisme de:histidine | tryptophane

WORLD HEALTH ORGANIZATION ICD-10: E70.8

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Others have searched : disorder of tyrosine metabolism disorders of tyrosine metabolism disorders of histidine metabolism disorder of cholesterol metabolism inborn error of metabolism inborn metabolic disorder metabolic disorder tryptophan metabolism Disorders tyrosine metabolism

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'Disorders tyrosine metabolism'

Date index:2021-03-22 -

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Translation of "Disorders tyrosine metabolism " (English → French) :

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