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Anemia due to riboflavin deficiency
Deficiency
E101ii
G-6-p-d deficiency
G6PD deficiency
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Haemolytic anaemia secondary to G6PD deficiency
Hemolytic anemia secondary to G6PD deficiency
Hexokinase deficiency
Mobility deficiency
Mobility difficulty
Mobility disability
Mobility impairment
PK
Pyruvate kinase
Riboflavin deficiency
Riboflavin-5'-phosphate
Riboflavin-5'-phosphate sodium
Triose-phosphate isomerase deficiency

Vertaling van "riboflavin deficiency " (Engels → Nederlands) :



Anemia due to riboflavin deficiency

anemie door riboflavinedeficiëntie


Providing riboflavin based on suboptimal food or fluid intake, iatrogenic deficiency or medical diagnosis.

behandeling met vitamine B2-supplement


E101ii | riboflavin-5'-phosphate | riboflavin-5'-phosphate sodium

E101ii | riboflavine-5'-fosfaat | riboflavine-5'-fosfaat-natrium


G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency

G6PD-deficiëntie


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


Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child

obesitas als gevolg van melanocortine-4-receptordeficiëntie


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

anemie (door) | deficiëntie van | pyruvaatkinase [PK] | anemie (door) | deficiëntie van | triosefosfaatisomerase | anemie (door) | hemolytisch niet-sferocytair (hereditair), type II | anemie (door) | deficiëntie van | hexokinase


Vitamin B12 deficiency anaemia due to intrinsic factor deficiency

anemie door vitamine B12-deficiëntie als gevolg van tekort aan 'intrinsic factor'


mobility deficiency | mobility difficulty | mobility disability | mobility impairment

beperkte mobiliteit | mobiele beperking




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Date index: 2020-12-13
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