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ADA
ADA Committee
ADA deficiency
Accommodation Deficiency Adjustment Committee
Ada program entity
Ada program module
Ada program unit
Adenosine deaminase
Adenosine deaminase deficiency
Congenital antithrombin III deficiency
Congenital deficiency of antithrombin III
Deficiency
Deficiency disease
G-6-p-d deficiency
G6PD deficiency
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Hexokinase deficiency
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Nutrition deficiency disease
Nutritional deficiency disease
PK
Pyruvate kinase
Triose-phosphate isomerase deficiency

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

ADA deficiency | adenosine deaminase deficiency

déficience en adénosine-désaminase | déficit en adénosine désaminase | déficit ADA | déficience en ADA


Adenosine deaminase [ADA] deficiency

Déficit en adénosine désaminase [ADA]


Accommodation Deficiency Adjustment Committee [ ADA Committee ]

Comité du rajustement compensatoire en matière de logement


combined immunodeficiency secondary to ADA enzyme deficiency

déficit immunitaire combiné sévère associé à un déficit en adénosine désaminase


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


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

déficit congénital en antithrombine III


Ada program entity [ Ada program module | Ada program unit ]

module de programme Ada [ entité de programme Ada ]


deficiency disease | nutrition deficiency disease | nutritional deficiency disease

maladie de carence | maladie par carence alimentaire


Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

Anémie (due à):déficit en:hexokinase | pyruvate kinase [PK] | triose-phosphate isomérase | hémolytique non sphérocytaire (héréditaire), type II


Vitamin B12 deficiency anaemia due to intrinsic factor deficiency

Anémie par carence en vitamine B12 due à une carence en facteur intrinsèque


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