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

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

hyperammoniëmische encefalopathie door carboanhydrase VA-deficiëntie

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Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism

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stofwisselingsstoornissen van aminozuren met vertakte keten en van vetzuren

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transitory endocrine and metabolic disturbances caused by the infant's response to maternal endocrine and metabolic factors, or its adjustment to extrauterine existence

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

voorbijgaande endocriene stoornissen en stofwisselingsstoornissen veroorzaakt door de reactie van de zuigeling op endocriene factoren en stofwisselingsfactoren van moeder, of op de aanpassing aan het extra-uteriene bestaan

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A type of metabolic myopathy described only in two sisters to date, presenting during childhood, and characterized clinically by growth failure, severe muscle weakness, and moderate sensorineural deafness and biochemically by metabolic acidosis, elev

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syndroom van mitochondriale myopathie, lactaatacidose en doofheid

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Tryptophan in oral dosage form

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product dat tryptofaan in orale vorm bevat

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describe the molecular basis of a disease to a patient | explain the metabolic basis of a disease to a patient | explain molecular basis of diseases to patients | explain the molecular basis of a disease to patients

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moleculaire basis van een ziekte aan patiënten uitleggen | uitleg geven aan patiënten over de moleculaire basis van een ziekte

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Anderen hebben gezocht naar : disorders of histidine metabolism tryptophan in oral dosage form basal metabolic rate glucose metabolism metabolism of glucose resting metabolic rate tryptophan tryptophan metabolism tryptophane Tryptophan metabolism

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Date index: 2023-05-01