WORDSCOPE MESSAGE : Wordscope Server is currently unavailable (Maintenance) - Please try again in a few minutes !
Boost Your Productivity !Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
Translation of "Déficit en facteur VII " (French → English) :
TERMINOLOGY
see also In-Context Translations below déficit en facteur VII
Factor 7 deficiency
SNOMEDCT-CA (trouble) / 37193007
SNOMEDCT-CA (trouble) / 37193007
Facteur VII de coagulation humain (proconvertine)
Autoprothrombin I
SNOMEDCT-CA (proconvertine) / 30804005
SNOMEDCT-CA (proconvertine) (substance) / 30804005
hyperlaxité de la peau par déficit en facteur de coagulation dépendant de la vitamine K
This syndrome has characteristics of hyperlaxity of the skin involving the entire body. It has been described in six patients. The phenotype is linked to a deficiency in vitamin K-dependent clotting factors and the syndrome has been associated with m
SNOMEDCT-BE (disorder) / 717941005
SNOMEDCT-BE (disorder) / 717941005
syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII
Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may
SNOMEDCT-BE (disorder) / 733028000
SNOMEDCT-BE (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may / 733028000
lipodystrophie par déficit en facteurs de croissance peptidiques
Hoepffner Dreyer Reimers syndrome
SNOMEDCT-BE (disorder) / 724176001
SNOMEDCT-BE (disorder) / 724176001
déficit en facteur C3 du complément
C3 deficiency
SNOMEDCT-BE (disorder) / 771443008
SNOMEDCT-BE (disorder) / 771443008
retard de croissance par déficit du facteur de croissance analogue à l'insuline type 1
Syndrome with the association of intrauterine and postnatal growth retardation, sensorineural deafness and intellectual deficit. The syndrome is extremely rare and only four cases have been reported in the literature so far. Additional clinical featu
SNOMEDCT-BE (disorder) / 724385009
SNOMEDCT-BE (disorder) / 724385009
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
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
déficit combiné en facteurs V et VIII
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
SNOMEDCT-BE (disorder) / 715559004
SNOMEDCT-BE (chromosome 18; q21) or in t / 715559004
déficit héréditaire combiné en facteurs de la coagulation dépendants de la vitamine K
A rare congenital bleeding disorder resulting from variably decreased levels of coagulation factors II, VII, IX and X, as well as natural anticoagulants protein C, protein S and protein Z. Other symptoms are often present, including developmental and
SNOMEDCT-BE (disorder) / 724356003
SNOMEDCT-BE (disorder) / 724356003
www.wordscope.com (v4.0.br.77)
Déficit en facteur VII
Date index:2024-02-03 -
Pour agences de traduction et traducteurs - For translation agencies & translators
Paris - Brussels - Montreal - Genève - Luxembourg - Madrid
Wordscope - Professional computer-assisted translation tools (CAT tools)
