Boost Your Productivity!Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
https://pro.wordscope.com
https://blog. wordscope .com
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
Stuart-Prower
Triose-phosphate isomerase deficiency
V
VII
X
XII
XIII

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

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


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


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

G6PD-deficiëntie


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


CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency

3-methylglutaconzuuracidurie type 7


Short stature due to primary acid-labile subunit (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3

kleine gestalte door primaire zuurlabiele subeenheiddeficiëntie


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


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


w