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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
Factor VII
Factor VII deficiency
Familia
G-6-p-d deficiency
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
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
Krabbe disease
Krabbe's disease
Najjar-Andersen syndrome
Proconvertin
Proconvertin deficiency
Prothrombinogen
SPCA
Serum accelerator
Serum prothrombin conversion accelerator
Stable factor
Stable factor deficiency
Sulfur deficient
Sulfur-deficient
Sulphur deficient
Sulphur-deficient

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

factor VII deficiency | stable factor deficiency | proconvertin deficiency

déficit en facteur VII | déficience en facteur VII | hypoproconvertinémie | maladie congénitale d'Alexander


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


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

déficit congénital en antithrombine III


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 ]


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


factor VII | proconvertin | prothrombinogen | serum accelerator | serum prothrombin conversion accelerator | stable factor

facteur VII | proconvertine


proconvertin [ factor VII | stable factor | serum prothrombin conversion accelerator | SPCA ]

proconvertine [ facteur VII ]


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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