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Anaemia due to glucose-6-phosphate dehydrogenase
Deficiency
Favism G6PD deficiency anaemia
G-6-p-d deficiency
G6PD
G6PD deficiency
G6PD deficiency anemia
GCL
Galactocerebrosidase deficiency
Galactosylceramide beta-galactosidase deficiency
Galc deficiency
Globoid cell leukodystrophy
Globoid cell leukoencephalopathy
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
HMP
Haemolytic anaemia secondary to G6PD deficiency
Hemolytic anemia secondary to G6PD deficiency
Krabbe disease
Krabbe's disease
Mobility deficiency
Mobility difficulty
Mobility disability
Mobility impairment
Shunt pathway

Vertaling van "G6PD deficiency " (Engels → Nederlands) :

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

G6PD-deficiëntie


G6PD deficiency anemia

anemie door deficiëntie van glucose-6-fosfaatdehydrogenase


Favism G6PD deficiency anaemia

anemie door G-6-PD-deficiëntie | favisme


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


Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency

anemie door deficiëntie van glucose-6-fosfaatdehydrogenase [G-6-PD]


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


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


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


CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency

3-methylglutaconzuuracidurie type 7


mobility deficiency | mobility difficulty | mobility disability | mobility impairment

beperkte mobiliteit | mobiele beperking


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