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]

déficit en CA-VA

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

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

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

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

encéphalopathie hyperammoniémique par déficit en anhydrase carbonique VA

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

metabolic disorder

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

perturbation du métabolisme

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

Disorders of:histidine metabolism | tryptophan metabolism

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

Anomalies du métabolisme de:histidine | tryptophane

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

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

Anderen hebben gezocht naar : 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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Date index: 2021-06-06