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Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Congenital antithrombin III deficiency
Congenital deficiency of antithrombin III
Deficiency
Familia
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
Hemolytic anemia secondary to G6PD deficiency
Hexokinase deficiency
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Najjar-Andersen syndrome
PK
PN
Pyridoxine
Pyridoxine deficiency
Pyridoxine deficiency anaemia
Pyridoxine-responsive NEC
Pyruvate kinase
Sideroblastic anaemia NOS
Sulfur deficient
Sulfur-deficient
Sulphur deficient
Sulphur-deficient
Triose-phosphate isomerase deficiency

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

pyridoxine deficiency anaemia
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
anémie par carence en vitamine B6
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Pyridoxine deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Carence en pyridoxine
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
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]
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]
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]
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]
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]
pyridoxine [ PN | 3-hydroxy-4,5-dimethylol-alpha-picoline | 5-hydroxy-6-methyl-3,4-pyridinedimethanol | 2-methyl-3-hydroxy-4,5-dihydroxymethylpridine | 2-methyl-4,5-bis(hydroxymethyl)-3-hydroxypyridine | 2-methyl-3-hydroxy-4,5-bis-(hydroxymethyl)pyridine | 2-methyl-3-hydroxy-4,5-di- ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
pyridoxine [ PN | 3-hydroxy-4,5-diméthylol-alpha-picoline | 5-hydroxy-6-méthyl-3,4-pyridinediméthanol | 2-méthyl-3-hydroxy-4,5-dihydroxyméthylpyridine | 2-méthyl-4,5-bis(hydroxyméthyl)-3-hydroxypyridine | 2-méthyl-3-hydroxy-4,5-bis-(hydroxyméthyl)pyridine | 2-méthyl-3-hydroxy-4,5-di ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [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]
Sideroblastic anaemia:NOS | pyridoxine-responsive NEC
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anémie sidéroblastique:SAI | réagissant à la pyridoxine NCA
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     g6pd deficiency     gsd iv     najjar-andersen syndrome     pyridoxine deficiency     sideroblastic anaemia nos     amylopectinosis     amylopectinosis brancher deficiency     brancher deficiency     brancher enzyme deficiency     congenital antithrombin iii deficiency     congenital deficiency of antithrombin iii     deficiency     familia     g-6-p-d deficiency     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     pyridoxine     pyridoxine deficiency anaemia     pyruvate kinase     sulfur deficient     sulfur-deficient     sulphur deficient     sulphur-deficient     triose-phosphate isomerase deficiency     


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Date index: 2021-05-16
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