Boost Your Productivity!Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
https://pro.wordscope.com
https://blog. wordscope .com
Anaemia Addison
Biermer
Congenital Factor VIII deficiency
Congenital afibrinogenaemia Deficiency AC globulin
Congenital clotting factor deficiency
Congenital coagulation factor deficiency
Congenital intrinsic factor deficiency
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
Hageman
Hereditary deficiency of other clotting factors
II
Labile
Pernicious
Proaccelerin
Prothrombin
Stable
Stuart-Prower
V
VII
X
XII
XIII

Vertaling van "Congenital clotting factor deficiency " (Engels → Nederlands) :

congenital clotting factor deficiency | congenital coagulation factor deficiency

erfelijke stollingsfactordeficiëntie


Anaemia:Addison | Biermer | pernicious (congenital) | Congenital intrinsic factor deficiency

anemie van | Addison | anemie van | Biermer | congenitale 'intrinsic factor'-deficiëntie | pernicieuze anemie (congenitaal)


Hereditary deficiency of other clotting factors

hereditaire deficiëntie van andere stollingsfactoren


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

lichaamshuidhyperlaxiteit als gevolg van vitamine K-afhankelijke coagulatiefactordeficiëntie


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

congenitale afibrinogenemie | deficiëntie van | AC globuline | deficiëntie van | proaccelerine | deficiëntie van factor | I [fibrinogeen] | deficiëntie van factor | II [protrombine] | deficiëntie van factor | V [labiel] | deficiëntie van factor | VII [stabiel] | deficiëntie van factor | X [Stuart-Prower] | deficiëntie van factor | XII [Hageman] | deficiëntie van factor | XIII [fibrinestabiliserend] | dysfibrinogenemie (congenitaal) | hypoproconvertinemie | ziekte van Owren


congenital Factor VIII deficiency

congenitale factor VIII deficiëntie


Congenital multiple pituitary hormone deficiency including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Rare when compared with t

gecombineerde hypofysehormoondeficiënties, genetische vormen




datacenter (1): www.wordscope.nl (v4.0.br)

'Congenital clotting factor deficiency' ->

Date index: 2022-05-22
w