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Translation of "Cancers multiples " (French → English) :
TERMINOLOGY
see also In-Context Translations below Cachexie maligne Cancer | Cancer généralisé | Cancers multiples | Carcinomatose | Carcinome | Tumeur maligne généralisée | de siège non précisé (primitif) (secondaire) | Siège primitif inconnu
Cancer | Carcinoma | Carcinomatosis | Generalized:cancer | malignancy | Malignancy | Multiple cancer | unspecified site (primary)(secondary) | Malignant cachexia Primary site unknown
WORLD HEALTH ORGANIZATION ICD-10: C80
WORLD HEALTH ORGANIZATION ICD-10: C80
Définition: Trouble, caractérisé à un moment quelconque au cours de la maladie, mais pas nécessairement de façon simultanée, par des tics moteurs multiples et par un ou plusieurs tics vocaux. Le trouble s'aggrave habituellement durant l'adolescence et persiste souvent à l'âge adulte. Les tics vocaux sont souvent multiples, avec des vocalisations, des râclements de gorge, et des grognements explosifs et répétés et parfois une émission de mots ou de phrases obscènes, associés, dans certains cas, à une échopraxie gestuelle pouvant également être obscène (copropraxie).
Definition: A form of tic disorder in which there are, or have been, multiple motor tics and one or more vocal tics, although these need not have occurred concurrently. The disorder usually worsens during adolescence and tends to persist into adult life. The vocal tics are often multiple with explosive repetitive vocalizations, throat-clearing, and grunting, and there may be the use of obscene words or phrases. Sometimes there is associated gestural echopraxia which may also be of an obscene nature (copropraxia).
WORLD HEALTH ORGANIZATION ICD-10: F95.2
WORLD HEALTH ORGANIZATION ICD-10: F95.2
Définition: Les principales caractéristiques sont des
symptômes physiques multiples, récurrents et variables dans le temps, persistant au moins deux ans. Dans la plupart des cas, les sujets entretiennent, depuis longtemps, des relations complexes avec les services médicaux, spécialisés et non spécialisés, et ont subi de nombreuses investigations ou interventions exploratrices négatives. Les symptômes peuvent renvoyer à n'importe quel système ou partie du corps. Le trouble a une évolution chronique et fluctuante, et s'accompagne souvent d'une altération du comportement social, interpersonnel et familial. Quand le trouble est de durée plus
...[+++] brève (moins de deux ans) ou quand il se caractérise par des symptômes moins évidents, on doit faire un diagnostic de trouble somatoforme indifférencié (F45.1). | Syndrome de Briquet Trouble psychosomatique multiple
Definition: Th
e main features are multiple, recurrent and frequently changing physical symptoms of at least two years' duration. Most patients have a long and complicated history of contact with both primary and specialist medical care services, during which many negative investigations or fruitless exploratory operations may have been carried out. Symptoms may be referred to any part or system of the body. The course of the disorder is chronic and fluctuating, and is often associated with disruption of social, interpersonal, and family behaviour. Short-lived (less than two years) and le
ss striking symptom ...[+++]patterns should be classified under undifferentiated somatoform disorder (F45.1). | Briquet's disorder Multiple psychosomatic disorderWORLD HEALTH ORGANIZATION ICD-10: F45.0
WORLD HEALTH ORGANIZATION ICD-10: F45.0
multiples plaies ouvertes au niveau de multiples régions du corps
Multiple open wounds of multiple body regions
SNOMEDCT-CA (trouble) / 762398003
SNOMEDCT-CA (trouble) / 762398003
cancer des trompes
Malignant tumour of fallopian tube
SNOMEDCT-BE (disorder) / 363444001
SNOMEDCT-BE (disorder) / 363444001
cancer du côlon héréditaire non polyposique
Lynch syndrome
SNOMEDCT-BE (disorder) / 315058005
SNOMEDCT-BE (disorder) / 315058005
syndrome héréditaire de prédisposition au cancer de l'ovaire
Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec
SNOMEDCT-BE (disorder) / 771080008
SNOMEDCT-BE (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec / 771080008
syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire
Breast cancer is the most common cancer in women, accounting for 25% of all new cases of cancer. Most cases are sporadic, while 5-10% are estimated to be due to an inherited predisposition. Autosomal dominant alterations in two genes, BRCA1 and BRCA2
SNOMEDCT-BE (disorder) / 718220008
SNOMEDCT-BE (disorder) / 718220008
dépistage d'un cancer
Screening for cancer
SNOMEDCT-BE (procedure) / 15886004
SNOMEDCT-BE (procedure) / 15886004
cancer de la verge
Penile Ca
SNOMEDCT-BE (disorder) / 363516004
SNOMEDCT-BE (disorder) / 363516004
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Cancers multiples
Date index:2021-06-28 -
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