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Affections du nerf crânien VII
Afibrinogénémie congénitale Carence en AC-globuline
Carence en facteur I
Déficit en facteur VII
Facteur VII de coagulation humain
Fibrinogène
Hageman
II
Labile
Morquio
Nerf crânien VII
Proaccélérine
Prothrombine
Sanfilippo
Stabilisant de la fibrine
Stable
Stuart-Prower
V
VII
X
XII
XIII

Translation of "VII " (French → English) :

TERMINOLOGY
see also In-Context Translations below
Facteur VII de coagulation humain (proconvertine)
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Autoprothrombin I
SNOMEDCT-CA (proconvertine) / 30804005
SNOMEDCT-CA (proconvertine) (substance) / 30804005
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https://browser.ihtsdotools.or (...) [HTML]
Nerf crânien VII
https://icd.who.int/browse10/2 (...) (...) [HTML]
7th cranial nerve
WORLD HEALTH ORGANIZATION ICD-10: S04.5
WORLD HEALTH ORGANIZATION ICD-10: S04.5
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
affections du nerf crânien VII
https://icd.who.int/browse10/2 (...) (...) [HTML]
disorders of 7th cranial nerve
WORLD HEALTH ORGANIZATION ICD-10: G51
WORLD HEALTH ORGANIZATION ICD-10: G51
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Carence en bêta-glucoronidase Mucopolysaccharidoses, type III, IV, VI, VII Syndrome de:Maroteaux-Lamy (léger) (sévère) | Morquio (-semblable à) (classique) | Sanfilippo (type B) (type C) (type D)
https://icd.who.int/browse10/2 (...) (...) [HTML]
Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome:Maroteaux-Lamy (mild)(severe) | Morquio(-like)(classic) | Sanfilippo (type B)(type C)(type D)
WORLD HEALTH ORGANIZATION ICD-10: E76.2
WORLD HEALTH ORGANIZATION ICD-10: E76.2
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
déficit en facteur VII
https://browser.ihtsdotools.or (...) (...) [HTML]
Factor 7 deficiency
SNOMEDCT-CA (trouble) / 37193007
SNOMEDCT-CA (trouble) / 37193007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Afibrinogénémie congénitale Carence en:AC-globuline | proaccélérine | Carence en facteur:I [fibrinogène] | II [prothrombine] | V [labile] | VII [stable] | X [Stuart-Prower] | XII [Hageman] | XIII [stabilisant de la fibrine] | Disfibrinogénémie (congénitale) Hypoproconvertinémie Maladie de Owren
https://icd.who.int/browse10/2 (...) (...) [HTML]
Congenital afibrinogenaemia Deficiency:AC globulin | proaccelerin | Deficiency of factor:I [fibrinogen] | II [prothrombin] | V [labile] | VII [stable] | X [Stuart-Prower] | XII [Hageman] | XIII [fibrin-stabilizing] | Dysfibrinogenaemia (congenital) Hypoproconvertinaemia Owren's disease
WORLD HEALTH ORGANIZATION ICD-10: D68.2
WORLD HEALTH ORGANIZATION ICD-10: D68.2
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
IN-CONTEXT TRANSLATIONS


Others have searched : afibrinogénémie congénitale carence en ac-globuline    carence en facteur    hageman    morquio    nerf crânien vii    sanfilippo    stuart-prower    affections du nerf crânien vii    déficit en facteur vii    fibrinogène    labile    proaccélérine    prothrombine    stabilisant de la fibrine    stable    VII    


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VII

Date index:2021-12-14 -

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