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-deficient
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Congenital antithrombin III deficiency
Congenital deficiency of antithrombin III
DAF syndrome
Deficiency disease
Deficient in
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
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Lipid histiocytosis
Lipoid histiocytosis
Najjar-Andersen syndrome
Neutrophil specific granule deficiency
Niemann-Pick disease
Nutrition deficiency disease
Nutritional deficiency disease
Poor
Secondary granule deficiency
Specific granule deficiency
Sphingomyelin lipidosis
Sphingomyelinase deficiency
Sulfur deficient
Sulfur-deficient
Sulphur deficient
Sulphur-deficient

Vertaling van "sphingomyelinase deficiency " (Engels → Frans) :

DAF syndrome | lipid histiocytosis | lipoid histiocytosis (classical phosphatide) | Niemann-Pick disease | sphingomyelin lipidosis | sphingomyelinase deficiency

histiocytose lipoïdique essentielle | maladie de Niemann-Pick | sphingomyélinose


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


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


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 ]


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

déficient en soufre


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

déficit congénital en antithrombine III


secondary granule deficiency | specific granule deficiency | neutrophil specific granule deficiency

déficit en granules secondaires


deficiency disease | nutrition deficiency disease | nutritional deficiency disease

maladie de carence | maladie par carence alimentaire


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

obésité par déficit du récepteur de la mélanocortine 4


poor [ -deficient | deficient in ]

déficitaire en [ pauvre en ]


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