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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
Congenital lactase deficiency
Deficiency
Deficiency disease
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
Hexokinase deficiency
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Lactase deficiency
Najjar-Andersen syndrome
Nutrition deficiency disease
Nutritional deficiency disease
PK
Pyruvate kinase
Secondary lactase deficiency
Sulfur deficient
Sulfur-deficient
Sulphur deficient
Sulphur-deficient
Triose-phosphate isomerase deficiency

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



lactase deficiency

déficience en lactase [ carence en lactase | insuffisance en lactase ]


Congenital lactase deficiency

ficit congénital en lactase


Secondary lactase deficiency

ficit secondaire en lactase


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


sulphur deficient [ sulphur-deficient | sulfur-deficient | sulfur deficient ]

déficient en soufre


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 ]


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

déficit congénital en antithrombine III


deficiency disease | nutrition deficiency disease | nutritional deficiency disease

maladie de carence | maladie par carence alimentaire


Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

Anémie (due à):déficit en:hexokinase | pyruvate kinase [PK] | triose-phosphate isomérase | hémolytique non sphérocytaire (héréditaire), type II


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