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Autoimmune primary ovarian failure
Autosomal dominant primary microcephaly
Autosomal recessive primary microcephaly
Cancer
Carate
Carcinoma
Carcinomatosis
Chancre
Deciduous
Dentia praecox Natal
First
First vaccination
Generalized cancer
Malignancy
Malignant cachexia Primary site unknown
Multiple cancer
Neonatal
Of pinta
Papule
Persistent
Premature eruption of tooth
Primary
Primary
Primary tooth
Primary vaccination
Retained
Shedding of primary
Tooth
Unspecified site

Translation of "Primary " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Chancre (primary) | Papule (primary) | of pinta [carate]

Chancre (initial) | Papule (initiale) | de la pinta [caraté]
WORLD HEALTH ORGANIZATION ICD-10: A67.0
WORLD HEALTH ORGANIZATION ICD-10: A67.0




primary | first

primaire | qui apparaît en premier lieu
UGENT - Medical terms -
UGENT - Medical terms -


Primary (idiopathic) autoimmune hemolytic anemia

anémie hémolytique auto-immune primaire (idiopathique)
SNOMEDCT-BE (idiopathic) autoimmune hemolytic anemia / 127049002
SNOMEDCT-BE (idiopathique) / 127049002


Dentia praecox Natal | Neonatal | tooth | Premature:eruption of tooth | shedding of primary [deciduous] tooth | Retained [persistent] primary tooth

Chute prématurée des dents temporaires Dent:natale | néonatale | précoce | Eruption dentaire prématurée Rétention dentaire [dents temporaires persistantes]
WORLD HEALTH ORGANIZATION ICD-10: K00.6
WORLD HEALTH ORGANIZATION ICD-10: K00.6


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


Autoimmune primary ovarian failure

Insuffisance ovarienne prématurée auto-immune
SNOMEDCT-BE (disorder) / 237790001
SNOMEDCT-BE (disorder) / 237790001


A surgically correctable form of primary hyperaldosteronism characterised by renin suppression, unilateral aldosterone hypersecretion, and moderate to severe hypertension secondary to hyperplasia of the adrenal gland. May be associated with hypokalae

hyperplasie surrénalienne unilatérale primitive
SNOMEDCT-BE (disorder) / 715868005
SNOMEDCT-BE (disorder) / 715868005


Autosomal recessive primary microcephaly

microcéphalie primaire autosomique récessive
SNOMEDCT-BE (disorder) / 715981004
SNOMEDCT-BE (disorder) / 715981004


Autosomal dominant primary microcephaly

microcéphalie primaire autosomique dominante
SNOMEDCT-BE (disorder) / 778070003
SNOMEDCT-BE (disorder) / 778070003
IN-CONTEXT TRANSLATIONS


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'Primary'

Date index:2023-04-01 -

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