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Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Congenital afibrinogenaemia Deficiency AC globulin
Deficiency
Deficiency of factor I
Familia
Fibrin-stabilizing
Fibrinogen
G-6-p-d deficiency
G6PD deficiency
GSD IV
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Glycogen storage disease type IV
Glycogenosis IV
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
Najjar-Andersen syndrome
PK
Proaccelerin
Prothrombin
Pyruvate kinase
Stable
Stuart-Prower
Switching MOST
Triose-phosphate isomerase deficiency
V
VII
X
XII
XIII

Traduction de «Mo-1 deficiency » (Anglais → Français) :

Mo-1 deficiency
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
déficit d'adhésion leucocytaire 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]
déficit en G6PD | déficit en glucose-6-phosphate-déshydrogénase
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]
anémie hémolytique par déficit en G6PD
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]
transistor MOS de commutation
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child
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obésité par déficit du récepteur de la mélanocortine 4
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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]
Anémie (due à):déficit en:hexokinase | pyruvate kinase [PK] | triose-phosphate isomérase | hémolytique non sphérocytaire (héréditaire), type II
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Andersen's disease [ Andersen disease | Najjar-Andersen syndrome | glycogenosis IV | glycogen storage disease type IV | GSD IV | alpha 1,4-glucan-6-glucosyl transferase deficiency | amylopectinosis brancher deficiency | brancher enzyme deficiency | brancher deficiency | amylopectinosis | familia ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
maladie d'Andersen [ glycogénose musculaire type IV ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anémie par carence en vitamine B12 due à une carence en facteur intrinsèque
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [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]
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]
CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
acidurie 3-méthylglutaconique type 7
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


D'autres ont cherché : andersen disease     andersen's disease     congenital afibrinogenaemia deficiency ac globulin     deficiency of factor     g6pd deficiency     gsd iv     hageman     mos digital element     mos switch     mos switching transistor     mo-1 deficiency     najjar-andersen syndrome     stuart-prower     amylopectinosis     amylopectinosis brancher deficiency     brancher deficiency     brancher enzyme deficiency     deficiency     familia     fibrin-stabilizing     fibrinogen     g-6-p-d deficiency     glucose 6-dehydrogenase deficiency     glucose-6-phosphate dehydrogenase deficiency     glycogen storage disease type iv     glycogenosis iv     hexokinase deficiency     labile     proaccelerin     prothrombin     pyruvate kinase     stable     switching most     triose-phosphate isomerase deficiency     Mo-1 deficiency     


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Date index: 2023-08-25
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