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Accelerator factor
Acid labile
Acid-labile
Asthenic
Congenital afibrinogenaemia Deficiency AC globulin
Deficiency of factor I
Disorder
Factor V
Fibrin-stabilizing
Fibrinogen
Hageman
Heat labile enterotoxin
Heat labile toxin
Heat-labile enterotoxin
Heat-labile toxin
II
LT
Labile
Labile diabetes
Labile factor
Organic emotionally labile
Owren factor
Plasma accelerator globulin
Plasma labile factor
Plasma prothrombins conversion factor
Proaccelerin
Prothrombin
Prothrombin accelerator
Stable
Stuart-Prower
V
VII
X
XII
XIII

Translation of "Labile factor " (English → French) :

factor V | proaccelerin | accelerator factor | Owren factor | labile factor | plasma accelerator globulin | plasma labile factor | plasma prothrombins conversion factor | prothrombin accelerator

facteur V | proaccélérine | accélérine | facteur labile | facteur accélérateur | facteur d'Owren
médecine > hématologie et sérologie | médecine > transfusion
médecine > hématologie et sérologie | médecine > transfusion


Short stature due to primary acid-labile subunit (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3

petite taille par déficit primaire en sous-unité acide labile
SNOMEDCT-BE (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3 / 721074002
SNOMEDCT-BE (disorder) / 721074002


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

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
WORLD HEALTH ORGANIZATION ICD-10: D68.2
WORLD HEALTH ORGANIZATION ICD-10: D68.2


heat-labile enterotoxin | LT | heat labile enterotoxin

entérotoxine thermolabile | LT
pharmacologie > toxicologie | biologie
pharmacologie > toxicologie | biologie


acid-labile [ acid labile ]

labile en milieu acide
Cattle Raising
Élevage des bovins


heat-labile toxin | heat labile toxin

toxine thermolabile
pharmacologie > toxicologie | biologie
pharmacologie > toxicologie | biologie


Labile diabetes

diabète sucré instable
SNOMEDCT-BE (finding) / 11530004
SNOMEDCT-BE (finding) / 11530004


Organic emotionally labile [asthenic] disorder

Labilité [asthénie] émotionnelle organique
WORLD HEALTH ORGANIZATION ICD-10: F06.6
WORLD HEALTH ORGANIZATION ICD-10: F06.6


Definition: A disorder characterized by emotional incontinence or lability, fatigability, and a variety of unpleasant physical sensations (e.g. dizziness) and pains, but arising as a consequence of an organic disorder.

Définition: Trouble caractérisé par une incontinence ou une labilité émotionnelles, une fatigabilité, et diverses sensations physiques désagréables (par exemple des vertiges) et par des douleurs, mais secondaire à une maladie organique.
WORLD HEALTH ORGANIZATION ICD-10: F06.6
WORLD HEALTH ORGANIZATION ICD-10: F06.6


An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in t

déficit combiné en facteurs V et VIII
SNOMEDCT-BE (chromosome 18; q21) or in t / 715559004
SNOMEDCT-BE (disorder) / 715559004




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'Labile factor'

Date index:2021-04-27 -

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