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Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Apertura thoracis inferior
Apertura thoracis superior
Brancher deficiency
Brancher enzyme deficiency
Congenital antithrombin III deficiency
Congenital deficiency of antithrombin III
Deficiency disease
Deficiency in thorax
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
Inferior aperture of thorax
Inferior thoracic aperture
Inferior thoracic opening
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Inlet of thorax
Lower thoracic opening
Najjar-Andersen syndrome
Neutrophil specific granule deficiency
Nutrition deficiency disease
Nutritional deficiency disease
Outlet of thorax
Secondary granule deficiency
Specific granule deficiency
Superior aperture of thorax
Superior thoracic aperture
Superior thoracic opening
Thoracic inlet
Thoracic outlet
Upper thoracic opening

Traduction de «deficiency in thorax » (Anglais → Français) :



inferior aperture of thorax [ inferior thoracic aperture | outlet of thorax | thoracic outlet | lower thoracic opening | inferior thoracic opening | apertura thoracis inferior ]

orifice inférieur du thorax [ apertura thoracis inferior ]


superior aperture of thorax [ superior thoracic aperture | inlet of thorax | superior thoracic opening | upper thoracic opening | thoracic inlet | apertura thoracis superior ]

orifice supérieur du thorax [ apertura thoracis superior ]


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


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


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


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

déficit en granules secondaires


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


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