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-deficient
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Congenital afibrinogenaemia Deficiency AC globulin
Congenital antithrombin III deficiency
Congenital deficiency of antithrombin III
Deficiency
Deficiency of factor I
Deficient in
Familia
Fibrin-stabilizing
Fibrinogen
G-6-p-d deficiency
G6PD deficiency
GCL
GSD IV
Galactocerebrosidase deficiency
Galactosylceramide beta-galactosidase deficiency
Galc deficiency
Globoid cell leukodystrophy
Globoid cell leukoencephalopathy
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
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Krabbe disease
Krabbe's disease
Labile
Najjar-Andersen syndrome
PK
Poor
Proaccelerin
Prothrombin
Pyruvate kinase
Stable
Stuart-Prower
Sulfur deficient
Sulfur-deficient
Sulphur deficient
Sulphur-deficient
Triose-phosphate isomerase deficiency
V
VII
X
XII
XIII

Traduction de «Hexokinase deficiency » (Anglais → Français) :

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]
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]
sulphur deficient [ sulphur-deficient | sulfur-deficient | sulfur deficient ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
déficient en soufre
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
congenital antithrombin III deficiency | congenital deficiency of antithrombin III | inherited antithrombin III deficiency | inherited deficiency in AT III
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
déficit congénital en antithrombine III
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [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]
galactocerebrosidase deficiency | galactosylceramide beta-galactosidase deficiency | Galc deficiency | globoid cell leukodystrophy | globoid cell leukoencephalopathy | Krabbe disease | Krabbe's disease | GCL [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
déficit en galactocérébrosidase | leucodystrophie à cellules globoïdes | leucodystrophie de Krabbe | maladie de Krabbe
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
poor [ -deficient | deficient in ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
déficitaire en [ pauvre en ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [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]
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]


D'autres ont cherché : andersen disease     andersen's disease     congenital afibrinogenaemia deficiency ac globulin     deficiency of factor     g6pd deficiency     gsd iv     galc deficiency     hageman     krabbe disease     krabbe's disease     najjar-andersen syndrome     stuart-prower     amylopectinosis     amylopectinosis brancher deficiency     brancher deficiency     brancher enzyme deficiency     congenital antithrombin iii deficiency     congenital deficiency of antithrombin iii     deficiency     deficient in     familia     fibrin-stabilizing     fibrinogen     g-6-p-d deficiency     galactocerebrosidase deficiency     galactosylceramide beta-galactosidase deficiency     globoid cell leukodystrophy     globoid cell leukoencephalopathy     glucose 6-dehydrogenase deficiency     glucose-6-phosphate dehydrogenase deficiency     glycogen storage disease type iv     glycogenosis iv     hexokinase deficiency     inherited antithrombin iii deficiency     inherited deficiency in at iii     labile     proaccelerin     prothrombin     pyruvate kinase     stable     sulfur deficient     sulfur-deficient     sulphur deficient     sulphur-deficient     triose-phosphate isomerase deficiency     Hexokinase deficiency     


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Date index: 2023-02-23
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