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Chronic familial erythremia
Congenital non-spherocytic anaemia
Congenital nonspherocytic anemia
Cooley's anemia
Cooley's syndrome
Cooley's-disease
Cooley-Lee syndrome
Dameshek's syndrome
Deficiency
Erythroblastic anemia
HMP
Heinz hereditary bodies anemia
Hereditary leptocytosis
Hereditary non spherocytic hemolytic anemia
Hereditary nonspherocytic anemia
Hexokinase deficiency
Marcocytic hereditary hemolytic anemia
Mediterranean anemia
Mediterranean disease
PK
Primary erythroblastic anemia
Pyruvate kinase
Shunt pathway
Target cell anemia
Target-oval cell syndrome
Thalassaemia major
Thalassemia major
Thalassemic syndrome
Triose-phosphate isomerase deficiency

Translation of "Hereditary nonspherocytic anemia " (English → French) :

congenital non-spherocytic anaemia | congenital nonspherocytic anemia | hereditary nonspherocytic anemia

anémie hémolytique congénitale non sphérocytaire
médecine > sémiologie et pathologie
médecine > sémiologie et pathologie


marcocytic hereditary hemolytic anemia

anémie hémolytique héréditaire et macrocytaire
IATE - Health
IATE - Health


Heinz hereditary bodies anemia

anémie hémolytique héréditaire à corpuscules de Heinz
IATE - Health
IATE - Health


Cooley's anemia | Cooley's-disease | Cooley's syndrome | Cooley-Lee syndrome | Dameshek's syndrome | chronic familial erythremia | erythroblastic anemia | hereditary leptocytosis | Mediterranean anemia | Mediterranean disease | primary erythroblastic anemia | target cell anemia | target-oval cell syndrome | thalassaemia major | thalassemia major | thalassemic syndrome

maladie de Cooley | anémie de Cooley | anémie érythroblastique familiale primitive | anémie méditerranéenne | anémie microcytaire familiale | érythrémie chronique familiale | hémo-ostéopathie de Cooley | leptocytose héréditaire | maladie méditerranéenne | syndrome de Cooley-Lee | thalassanémie | thalassémie érythroblastique familiale génotypique | thalassémie majeure | anémie érythrémique
biologie > cytogénétique | médecine > hématologie et sérologie
biologie > cytogénétique | médecine > hématologie et sérologie


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


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
WORLD HEALTH ORGANIZATION ICD-10: D55.2
WORLD HEALTH ORGANIZATION ICD-10: D55.2


hereditary non spherocytic hemolytic anemia

anémie héréditaire hémolytique et asphérocytaire
IATE - Health
IATE - Health


A rare hereditary red cell membrane defect characterized by the presence of oval-shaped erythrocytes. Most patients are asymptomatic or occasionally have mild symptoms such as pallor, jaundice, anemia and gallstones. The disease is common in Southeas

ovalocytose de l'Asie du Sud-Est
SNOMEDCT-BE (disorder) / 723623002
SNOMEDCT-BE (disorder) / 723623002




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'Hereditary nonspherocytic anemia'

Date index:2022-06-30 -

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