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