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90-Mo
99-Mo
Congenital afibrinogenaemia Deficiency AC globulin
Deficiency
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
G-6-p-d deficiency
G6PD deficiency
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Haemolytic anaemia secondary to G6PD deficiency
Hageman
Hemolytic anemia secondary to G6PD deficiency
Hexokinase deficiency
II
Labile
MOS digital element
MOS switch
MOS switching transistor
Mo-1 deficiency
Mo-cap
Motion capture
Motion capturing
PK
Proaccelerin
Prothrombin
Pyruvate kinase
Stable
Stuart-Prower
Switching MOST
Triose-phosphate isomerase deficiency
V
VII
X
XII
XIII

Vertaling van "Mo-1 deficiency " (Engels → Nederlands) :

Mo-1 deficiency
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
leukocytadhesiedeficiëntie type I
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
G6PD-deficiëntie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
haemolytic anaemia secondary to G6PD deficiency | haemolytic anaemia secondary to glucose-6-phosphate dehydrogenase deficiency | hemolytic anemia secondary to G6PD deficiency | hemolytic anemia secondary to glucose-6-phosphate dehydrogenase deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
fosfaatdehydrogenase-deficiëntie | hemolytische anemie door G6PD-deficiëntie | hemolytische anemie door glucose-6
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
MOS digital element | MOS switch | MOS switching transistor | switching MOST
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
MOS-schakeltransistor
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
99-Mo
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
molybdeen-99
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
90-Mo
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
molybdeen-90
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
anemie (door) | deficiëntie van | pyruvaatkinase [PK] | anemie (door) | deficiëntie van | triosefosfaatisomerase | anemie (door) | hemolytisch niet-sferocytair (hereditair), type II | anemie (door) | deficiëntie van | hexokinase
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
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]
motion capturing | Mo-cap | motion capture
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
MoCap | motion capture
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]


Anderen hebben gezocht naar : congenital afibrinogenaemia deficiency ac globulin     deficiency of factor     g6pd deficiency     hageman     mos digital element     mos switch     mos switching transistor     mo-1 deficiency     mo-cap     stuart-prower     deficiency     fibrin-stabilizing     fibrinogen     g-6-p-d deficiency     glucose 6-dehydrogenase deficiency     glucose-6-phosphate dehydrogenase deficiency     hexokinase deficiency     labile     motion capture     motion capturing     proaccelerin     prothrombin     pyruvate kinase     stable     switching most     triose-phosphate isomerase deficiency     Mo-1 deficiency     


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Date index: 2022-10-12
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