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Amylopectinosis
Amylopectinosis brancher deficiency
Anaemia due to glucose-6-phosphate dehydrogenase
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Congenital antithrombin III deficiency
Congenital deficiency of antithrombin III
Deficiency
Deficiency disease
Familia
Favism G6PD deficiency anaemia
G-6-p-d deficiency
G6PD
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
Glucose-6-phosphate deshydrogenase deficiency
Glycogen storage disease type IV
Glycogenosis IV
HMP
Haemolytic anaemia secondary to G6PD deficiency
Hemolytic anemia secondary to G6PD deficiency
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Krabbe disease
Krabbe's disease
Najjar-Andersen syndrome
Nutrition deficiency disease
Nutritional deficiency disease
Shunt pathway

Traduction de «G6PD deficiency » (Anglais → Français) :

G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency

déficit en G6PD | déficit en glucose-6-phosphate-déshydrogénase


Favism G6PD deficiency anaemia

Anémie par carence en G6PD Favisme


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

anémie hémolytique par déficit en G6PD


glucose-6-phosphate deshydrogenase deficiency | G6PD deficiency

déficit en G6PD | G 6 PD | G-6-PD | G-6-P-D


Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency

Anémie due à une carence en glucose-6-phosphate déshydrogénase [G6PD]


Anaemia (due to):enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway | haemolytic nonspherocytic (hereditary), type I

Anémie (due à):déficit enzymatique, excepté G6PD, de la voie de l'hexose monophosphate [HMP] | hémolytique non sphérocytaire (héréditaire), type I


congenital antithrombin III deficiency | congenital deficiency of antithrombin III | inherited antithrombin III deficiency | inherited deficiency in AT III

déficit congénital en antithrombine III


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 ]

maladie d'Andersen [ glycogénose musculaire type IV ]


galactocerebrosidase deficiency | galactosylceramide beta-galactosidase deficiency | Galc deficiency | globoid cell leukodystrophy | globoid cell leukoencephalopathy | Krabbe disease | Krabbe's disease | GCL [Abbr.]

déficit en galactocérébrosidase | leucodystrophie à cellules globoïdes | leucodystrophie de Krabbe | maladie de Krabbe


deficiency disease | nutrition deficiency disease | nutritional deficiency disease

maladie de carence | maladie par carence alimentaire


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