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Congenital afibrinogenaemia Deficiency AC globulin
Deficiency
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
G-6-p-d deficiency
G6PD deficiency
GCL
Galactocerebrosidase deficiency
Galactosylceramide beta-galactosidase deficiency
Galc deficiency
Globoid cell leukodystrophy
Globoid cell leukoencephalopathy
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Haemolytic anaemia secondary to G6PD deficiency
Hageman
Hemolytic anemia secondary to G6PD deficiency
Hexokinase deficiency
II
Krabbe disease
Krabbe's disease
Labile
Mobility deficiency
Mobility difficulty
Mobility disability
Mobility impairment
PK
Proaccelerin
Prothrombin
Pyruvate kinase
Stable
Strontium deficiency
Strontium ranelate
Stuart-Prower
Triose-phosphate isomerase deficiency
V
VII
X
XII
XIII

Traduction de «strontium deficiency » (Anglais → Néerlandais) :



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


galactocerebrosidase deficiency | galactosylceramide beta-galactosidase deficiency | Galc deficiency | globoid cell leukodystrophy | globoid cell leukoencephalopathy | Krabbe disease | Krabbe's disease | GCL [Abbr.]

globoïdcel leukodystrofie | ziekte van Krabbe




Drug reaction with eosinophilia and systemic symptoms due to strontium ranelate

DRESS-syndroom door strontiumranelaat


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'


Congenital afibrinogenaemia Deficiency:AC globulin | proaccelerin | Deficiency of factor:I [fibrinogen] | II [prothrombin] | V [labile] | VII [stable] | X [Stuart-Prower] | XII [Hageman] | XIII [fibrin-stabilizing] | Dysfibrinogenaemia (congenital) Hypoproconvertinaemia Owren's disease

congenitale afibrinogenemie | deficiëntie van | AC globuline | deficiëntie van | proaccelerine | deficiëntie van factor | I [fibrinogeen] | deficiëntie van factor | II [protrombine] | deficiëntie van factor | V [labiel] | deficiëntie van factor | VII [stabiel] | deficiëntie van factor | X [Stuart-Prower] | deficiëntie van factor | XII [Hageman] | deficiëntie van factor | XIII [fibrinestabiliserend] | dysfibrinogenemie (congenitaal) | hypoproconvertinemie | ziekte van Owren


mobility deficiency | mobility difficulty | mobility disability | mobility impairment

beperkte mobiliteit | mobiele beperking


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