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Acquired haemolytic icterus
Acquired hemolytic icterus
Fetal icterus
Fetal jaundice
Foetal icterus
Foetal jaundice
HMP
Haemoglobinuria
Haemolytic anaemia
Haemolytic anaemia cold type
Haemolytic anaemia secondary to G6PD deficiency
Haemolytic icterus
Hemolytic anemia secondary to G6PD deficiency
Hemolytic icterus
Icterus
Jaundice
Perinatal haemolytic jaundice
Shunt pathway
Warm type

Traduction de «Haemolytic icterus » (Anglais → Néerlandais) :

acquired haemolytic icterus | acquired hemolytic icterus | haemolytic icterus | hemolytic icterus

hemolytische icterus


Acholuric (familial) jaundice Congenital (spherocytic) haemolytic icterus Minkowski-Chauffard syndrome

acholurische (familiale) geelzucht | congenitale (sferocytaire-) hemolytische-icterus | syndroom van Minkowski-Chauffard


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

fosfaatdehydrogenase-deficiëntie | hemolytische anemie door G6PD-deficiëntie | hemolytische anemie door glucose-6


Autoimmune haemolytic disease (cold type)(warm type) Chronic cold haemagglutinin disease Cold agglutinin:disease | haemoglobinuria | Haemolytic anaemia:cold type (secondary)(symptomatic) | warm type (secondary)(symptomatic)

auto-immune hemolytische-ziekte (koud type)(warm type) | chronische koudehemagglutinineziekte | hemolytische anemie | koud type (secundair)(symptomatisch) | hemolytische anemie | warm type (secundair)(symptomatisch) | koudeagglutinine | hemoglobinurie | koudeagglutinine | ziekte


Hemolytic uremic syndrome with either a family history of haemolytic uremic syndrome or a genetic mutation known to cause haemolytic uremic syndrome, or both.

familiair hemolytisch-uremisch syndroom


fetal icterus | fetal jaundice | foetal icterus | foetal jaundice

foetale icterus




Perinatal haemolytic jaundice

perinatale geelzucht door excessieve hemolyse




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

anemie (door) | enzymdeficiënties, behalve G-6-PD, verband houdend met hexosemonofosfaat-shuntbaan [HMP-shuntbaan] | anemie (door) | hemolytisch niet-sferocytair (hereditair), type I




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'Haemolytic icterus' ->

Date index: 2023-02-27
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