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Abcess of liver
Abscess of the liver
Amyloidosis cutis
Amyloidosis of the liver
Amyloidosis of the skin
Canadian Association for the Study of the Liver
Hepatic abscess
Hepatic amyloidosis
Hepatic metastasis
Liver access
Liver amyloidosis
Liver metastasis
Metastasis in the liver
Primary cancer of the liver
Primary liver cancer

Translation of "amyloidosis the liver " (English → French) :

hepatic amyloidosis [ amyloidosis of the liver | liver amyloidosis ]

amyloïdose hépatique [ amylose hépatique | amyloïdose du foie ]
Animal Diseases
Maladies des animaux


amyloidosis cutis | amyloidosis of the skin

amyloïdose cutanée
IATE - Health
IATE - Health


Squamous cell carcinoma of liver and intrahepatic biliary tract is an extremely rare primary malignant liver and biliary tract epithelial neoplasm originating in the intrahepatic bile duct epithelium histologically characterized by the presence of ke

carcinome épidermoïde du foie et des voies biliaires intrahépatiques
SNOMEDCT-BE (disorder) / 770684008
SNOMEDCT-BE (disorder) / 770684008


hepatic metastasis | liver metastasis | metastasis in the liver

métastase hépatique
IATE - Health
IATE - Health


abscess of the liver | abcess of liver | hepatic abscess | liver access

abcès du foie
médecine
médecine


primary liver cancer [ primary cancer of the liver ]

cancer primitif du foie
Liver and Biliary Ducts
Foie et voies biliaires


Canadian Association for the Study of the Liver

Association canadienne pour l'étude du foie
National Bodies and Committees (Canadian) | Liver and Biliary Ducts
Organismes et comités nationaux canadiens | Foie et voies biliaires


hereditary cerebral hemorrhage with amyloidosis of the Dutch type; HCHWA-Dutch

hémorragie cérébrale héréditaire avec amyloïdose de type hollandais
IATE - Health
IATE - Health


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


A genetic disorder with characteristics of the appearance of numerous cysts spread throughout the liver. Women are predominantly affected and have a larger number of cysts than affected males. Cysts are undetectable early in life and usually appear a

polykystose hépatique isolée
SNOMEDCT-BE (disorder) / 716196007
SNOMEDCT-BE (disorder) / 716196007




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'amyloidosis the liver'

Date index:2022-08-02 -

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