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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
II
Labile
Pernicious
Proaccelerin
Prothrombin
Stable
Stuart-Prower
V
VII
X
XII
XIII

Vertaling van "congenital intrinsic factor deficiency " (Engels → Nederlands) :

Anaemia:Addison | Biermer | pernicious (congenital) | Congenital intrinsic factor deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
anemie van | Addison | anemie van | Biermer | congenitale 'intrinsic factor'-deficiëntie | pernicieuze anemie (congenitaal)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
congenital clotting factor deficiency | congenital coagulation factor deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
erfelijke stollingsfactordeficiëntie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
anemie door vitamine B12-deficiëntie als gevolg van tekort aan 'intrinsic factor'
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
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]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
congenital Factor VIII deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
congenitale factor VIII deficiëntie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
gecombineerde hypofysehormoondeficiënties, genetische vormen
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : anaemia addison     biermer     congenital afibrinogenaemia deficiency ac globulin     congenital intrinsic factor deficiency     deficiency of factor     hageman     stuart-prower     congenital factor viii deficiency     congenital clotting factor deficiency     congenital coagulation factor deficiency     fibrin-stabilizing     fibrinogen     labile     pernicious     proaccelerin     prothrombin     stable     


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Date index: 2021-10-15
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