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Translation of "nec with hepatic failure " (English → French) :
TERMINOLOGY
see also In-Context Translations below hepatic:coma NOS | encephalopathy NOS | hepatitis:acute | fulminant | malignant | NEC, with hepatic failure | liver (cell) necrosis with hepatic failure yellow liver atrophy or dystrophy
atrophie ou dystrophie jaune du foie coma | encéphalopathie | hépatique SAI | hépatite:aiguë | fulminante | maligne | NCA, avec insuffisance hépatique | nécrose des hépatocytes avec insuffisance hépatique
WORLD HEALTH ORGANIZATION ICD-10: K72
WORLD HEALTH ORGANIZATION ICD-10: K72
Alcoholic hepatic failure:NOS | acute | chronic | subacute | with or without hepatic coma
Insuffisance hépatique alcoolique:SAI | aiguë | avec ou sans coma hépatique | chronique | subaiguë
WORLD HEALTH ORGANIZATION ICD-10: K70.4
WORLD HEALTH ORGANIZATION ICD-10: K70.4
A mitochondrial fatty acid oxidation disorder characterized by hyperinsulinemic hypoglycemia with seizures, and in one case fulminant hepatic failure. Less than 10 cases have been reported to date. The disease can present in infancy or early childhoo
hyperinsulinisme par déficit en 3-hydroxylacyl-CoA déshydrogénase des acides gras à chaîne courte
SNOMEDCT-BE (disorder) / 721236002
SNOMEDCT-BE (disorder) / 721236002
A rare genetic hepatic disease characterized by massive hepatomegaly, moderate to severe transient hypertriglyceridemia and hepatic steatosis (followed by fibrosis) manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fa
hypertriglycéridémie transitoire et stéatose hépatique du nourrisson
SNOMEDCT-CA (followed by fibrosis) manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fa / 773649005
SNOMEDCT-CA (trouble) / 773649005
A rare genetic parenchymal hepatic disease with characteristics of acute liver failure that occurs in the first year of life, which manifests with failure to thrive, hypotonia, moderate global developmental delay, seizures, abnormal liver function te
syndrome d'insuffisance hépatique aigüe infantile-manifestations multisystémiques
SNOMEDCT-BE (disorder) / 774207004
SNOMEDCT-BE (disorder) / 774207004
An extremely rare genetic endocrine disease with characteristics of primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia w
adrénomyodystrophie
SNOMEDCT-BE (disorder) / 763311001
SNOMEDCT-BE (disorder) / 763311001
www.wordscope.com (v4.0.br.77)
'nec with hepatic failure'
Date index:2022-02-14 -
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