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Translation of "Secondary cancer " (English → French) :
TERMINOLOGY
see also In-Context Translations below Secondary cancer
métastase
SNOMEDCT-BE (disorder) / 128462008
SNOMEDCT-BE (disorder) / 128462008
Secondary cancer of brain
métastase cervicale
SNOMEDCT-BE (disorder) / 94225005
SNOMEDCT-BE (disorder) / 94225005
Secondary cancer of lung
tumeur maligne secondaire du poumon
SNOMEDCT-BE (disorder) / 94391008
SNOMEDCT-BE (disorder) / 94391008
Secondary cancer of kidney
tumeur maligne secondaire du rein
SNOMEDCT-BE (disorder) / 94360002
SNOMEDCT-BE (disorder) / 94360002
Human immunodeficiency virus with secondary cancers
virus de l'immunodéficience humaine et cancers secondaires
SNOMEDCT-CA (trouble) / 186709004
SNOMEDCT-CA (trouble) / 186709004
Cancer | Carcinoma | Carcinomatosis | Generalized:cancer | malignancy | Malignancy | Multiple cancer | unspecified site (primary)(secondary) | Malignant cachexia Primary site unknown
Cachexie maligne Cancer | Cancer généralisé | Cancers multiples | Carcinomatose | Carcinome | Tumeur maligne généralisée | de siège non précisé (primitif) (secondaire) | Siège primitif inconnu
WORLD HEALTH ORGANIZATION ICD-10: C80
WORLD HEALTH ORGANIZATION ICD-10: C80
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
syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire
SNOMEDCT-BE (disorder) / 718220008
SNOMEDCT-BE (disorder) / 718220008
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
syndrome héréditaire de prédisposition au cancer de l'ovaire
SNOMEDCT-BE (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec / 771080008
SNOMEDCT-BE (disorder) / 771080008
A rare inherited cancer-predisposing syndrome characterized by the development of a broad spectrum of malignancies during childhood, including mainly brain, hematological and gastrointestinal cancers, although embryonic and other tumors have also bee
syndrome de déficit constitutionnel de la réparation des mésappariements
SNOMEDCT-BE (disorder) / 764946008
SNOMEDCT-BE (disorder) / 764946008
Autoimmune haemolytic disease (cold type)(warm type) Chronic cold haemagglutinin disease Cold agglutinin:disease | haemoglobinuria | Haemolytic anaemia:cold type (secondary)(symptomatic) | warm type (secondary)(symptomatic)
Anémie hémolytique:type chaud (secondaire) (symptomatique) | type froid (secondaire) (symptomatique) | Hémoglobinurie à agglutinines froides Maladie (à):agglutinines froides | chronique à hémagglutinines froides | hémolytique auto-immune (type chaud) (type froid)
WORLD HEALTH ORGANIZATION ICD-10: D59.1
WORLD HEALTH ORGANIZATION ICD-10: D59.1
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'Secondary cancer'
Date index:2022-12-30 -
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