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Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Drug-induced enzyme deficiency anaemia
Enzyme deficiency
Familia
GSD IV
Glycogen storage disease type IV
Glycogenosis IV
HMP
Najjar-Andersen syndrome
Shunt pathway

Translation of "Brancher enzyme deficiency " (English → French) :

brancher enzyme deficiency [ amylopectinosis ]

déficience en enzyme branchante
Blood
Sang


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 ]
Endocrine System and Metabolism | Liver and Biliary Ducts
Systèmes endocrinien et métabolique | Foie et voies biliaires


enzyme deficiency

déficience enzymatique
IATE - Health
IATE - Health


combined immunodeficiency secondary to ADA enzyme deficiency

déficit immunitaire combiné sévère associé à un déficit en adénosine désaminase
Immunology
Immunologie


Anaemia (due to):enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway | haemolytic nonspherocytic (hereditary), type I

Anémie (due à):déficit enzymatique, excepté G6PD, de la voie de l'hexose monophosphate [HMP] | hémolytique non sphérocytaire (héréditaire), type I
WORLD HEALTH ORGANIZATION ICD-10: D55.1
WORLD HEALTH ORGANIZATION ICD-10: D55.1


Congenital adrenogenital disorders associated with enzyme deficiency

Anomalies génito-surrénaliennes congénitales liées à un déficit enzymatique
WORLD HEALTH ORGANIZATION ICD-10: E25.0
WORLD HEALTH ORGANIZATION ICD-10: E25.0


Drug-induced enzyme deficiency anaemia

Anémie par déficit enzymatique, due à des médicaments
WORLD HEALTH ORGANIZATION ICD-10: D59.2
WORLD HEALTH ORGANIZATION ICD-10: D59.2




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'Brancher enzyme deficiency'

Date index:2022-12-16 -

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