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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
Deficiency
Deficiency disease
Factor XI 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
Haemophilia C Plasma thromboplastin antecedent
Hemolytic anemia secondary to G6PD deficiency
Hemophilia C
Hexokinase deficiency
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Krabbe disease
Krabbe's disease
Najjar-Andersen syndrome
Nutrition deficiency disease
Nutritional deficiency disease
PK
PTA
PTA deficiency
Plasma thromboplastin antecedent deficiency
Pyruvate kinase
Rosenthal's syndrome
Triose-phosphate isomerase deficiency

Translation of "PTA deficiency " (English → French) :

factor XI deficiency | hemophilia C | Rosenthal's syndrome | plasma thromboplastin antecedent deficiency | PTA deficiency

déficit en facteur XI | déficience en facteur XI | maladie de Rosenthal | hémophilie C | syndrome de Rosenthal


Haemophilia C Plasma thromboplastin antecedent [PTA] deficiency

Déficit en précurseur de thromboplastine plasmatique [PTA] Hémophilie C


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


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


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


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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