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Afibrinogenaemia
Congenital afibrinogenaemia
Congenital afibrinogenaemia Deficiency AC globulin
DIC
Defibrination syndrome
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
Following conditions classifiable to O00-O07
Fulminans
Hageman
II
Intravascular coagulation
Labile
Proaccelerin
Prothrombin
Stable
Stuart-Prower
V
VII
X
XII
XIII

Traduction de «afibrinogenaemia » (Anglais → Français) :

afibrinogenaemia
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
afibrinogénémie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Afibrinogenaemia, acquired Consumption coagulopathy Diffuse or disseminated intravascular coagulation [DIC] Fibrinolytic haemorrhage, acquired Purpura:fibrinolytic | fulminans
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Afibrinogénémie acquise Coagulation intravasculaire diffuse ou disséminée [CIVD] Coagulopathie de consommation Hémorragie fibrinolytique acquise Purpura:fibrinolytique | fulminans
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Afibrinogenaemia | Defibrination syndrome | Intravascular coagulation | following conditions classifiable to O00-O07
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Afibrinogénémie | Coagulation intravasculaire | Syndrome de défibrination | survenant après les états classés en O00-O07
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
congenital afibrinogenaemia
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afibrinogénémie congénitale
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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]


D'autres ont cherché : afibrinogenaemia     congenital afibrinogenaemia deficiency ac globulin     defibrination syndrome     deficiency of factor     fibrinolytic haemorrhage acquired purpura fibrinolytic     hageman     intravascular coagulation     stuart-prower     congenital afibrinogenaemia     fibrin-stabilizing     fibrinogen     following conditions classifiable to o00-o07     fulminans     labile     proaccelerin     prothrombin     stable     


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Date index: 2021-06-10
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