Übersetzung für "brancher deficiency " (Englisch → Französisch) :

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maladie d'Andersen [ glycogénose musculaire type IV ]

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brancher enzyme deficiency [ amylopectinosis ]

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déficience en enzyme branchante

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G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency

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déficit en G6PD | déficit en glucose-6-phosphate-déshydrogénase

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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

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anémie hémolytique par déficit en G6PD

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

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déficit congénital en antithrombine III

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

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déficient en soufre

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déficit en galactocérébrosidase | leucodystrophie à cellules globoïdes | leucodystrophie de Krabbe | maladie de Krabbe

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

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déficit en granules secondaires

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deficiency disease | nutrition deficiency disease | nutritional deficiency disease

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maladie de carence | maladie par carence alimentaire

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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

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obésité par déficit du récepteur de la mélanocortine 4

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Andere haben gesucht : andersen disease andersen's disease g6pd deficiency gsd iv galc deficiency krabbe disease krabbe's disease najjar-andersen syndrome amylopectinosis amylopectinosis brancher deficiency brancher deficiency brancher enzyme deficiency congenital antithrombin iii deficiency congenital deficiency of antithrombin iii deficiency disease familia g-6-p-d deficiency galactocerebrosidase deficiency galactosylceramide beta-galactosidase deficiency globoid cell leukodystrophy globoid cell leukoencephalopathy glucose 6-dehydrogenase deficiency glucose-6-phosphate dehydrogenase deficiency glycogen storage disease type iv glycogenosis iv inherited antithrombin iii deficiency inherited deficiency in at iii neutrophil specific granule deficiency nutrition deficiency disease nutritional deficiency disease secondary granule deficiency specific granule deficiency sulfur deficient sulfur-deficient sulphur deficient sulphur-deficient

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'brancher deficiency' ->

Date index: 2022-03-07