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Colon disease
Colonopathy
Diverticular disease of the colon
Functional cardiac disease
Functional colonic disease
Other congenital functional disorders of colon

Translation of "Functional colonic disease " (English → French) :

functional colonic disease

colopathie fonctionnelle
IATE - Health
IATE - Health


colonopathy | colon disease

colopathie | affection du côlon
UGENT - Medical terms -
UGENT - Medical terms -


functional cardiac disease

maladie fonctionelle cardiaque
IATE - Health
IATE - Health


Anomalies of pupillary function in diseases classified elsewhere

Anomalies fonctionnelles de la pupille au cours de maladies classées ailleurs
WORLD HEALTH ORGANIZATION ICD-10: H58.0*
WORLD HEALTH ORGANIZATION ICD-10: H58.0*


diverticular disease of the colon

maladie diverticulaire du côlon
IATE - Health
IATE - Health


diverticular disease of the colon

diverticulose colique | maladie diverticulaire
médecine > gériatrie
médecine > gériatrie


International Society for the Study of Diseases of the Colon and Rectum

Société internationale pour l'étude des maladies du côlon et du rectum
International Bodies and Committees
Organismes et comités internationaux


Definition: Dementia in Alzheimer's disease with onset before the age of 65, with a relatively rapid deteriorating course and with marked multiple disorders of the higher cortical functions. | Alzheimer's disease, type 2 Presenile dementia, Alzheimer's type Primary degenerative dementia of the Alzheimer's type, presenile onset

Définition: Démence de la maladie d'Alzheimer survenant avant l'âge de 65 ans, évoluant assez rapidement vers une détérioration et comportant de multiples perturbations marquées des fonctions corticales supérieures. | Démence dégénérative primaire de type Alzheimer, à début présénile Démence présénile, de type Alzheimer Maladie d'Alzheimer, type 2
WORLD HEALTH ORGANIZATION ICD-10: F00.0*
WORLD HEALTH ORGANIZATION ICD-10: F00.0*


Other congenital functional disorders of colon

Autres anomalies fonctionnelles congénitales du côlon
WORLD HEALTH ORGANIZATION ICD-10: Q43.2
WORLD HEALTH ORGANIZATION ICD-10: Q43.2


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




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'Functional colonic disease'

Date index:2022-02-17 -

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