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Congenital afibrinogenaemia Deficiency AC globulin
Deficiency
Deficiency of A-ase
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

Traduction de «Deficiency A-ase » (Anglais → Néerlandais) :

Deficiency of A-ase
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asparaginasedeficiëntie
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G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
G6PD-deficiëntie
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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
fosfaatdehydrogenase-deficiëntie | hemolytische anemie door G6PD-deficiëntie | hemolytische anemie door glucose-6
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
galactocerebrosidase deficiency | galactosylceramide beta-galactosidase deficiency | Galc deficiency | globoid cell leukodystrophy | globoid cell leukoencephalopathy | Krabbe disease | Krabbe's disease | GCL [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
globoïdcel leukodystrofie | ziekte van Krabbe
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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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
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obesitas als gevolg van melanocortine-4-receptordeficiëntie
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Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
anemie (door) | deficiëntie van | pyruvaatkinase [PK] | anemie (door) | deficiëntie van | triosefosfaatisomerase | anemie (door) | hemolytisch niet-sferocytair (hereditair), type II | anemie (door) | deficiëntie van | hexokinase
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https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency
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3-methylglutaconzuuracidurie type 7
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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
anemie door vitamine B12-deficiëntie als gevolg van tekort aan 'intrinsic factor'
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https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
mobility deficiency | mobility difficulty | mobility disability | mobility impairment
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beperkte mobiliteit | mobiele beperking
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]


D'autres ont cherché : congenital afibrinogenaemia deficiency ac globulin     deficiency of a-ase     deficiency of factor     g6pd deficiency     galc deficiency     hageman     krabbe disease     krabbe's disease     stuart-prower     deficiency     fibrin-stabilizing     fibrinogen     g-6-p-d deficiency     galactocerebrosidase deficiency     galactosylceramide beta-galactosidase deficiency     globoid cell leukodystrophy     globoid cell leukoencephalopathy     glucose 6-dehydrogenase deficiency     glucose-6-phosphate dehydrogenase deficiency     hexokinase deficiency     labile     mobility deficiency     mobility difficulty     mobility disability     mobility impairment     proaccelerin     prothrombin     pyruvate kinase     stable     triose-phosphate isomerase deficiency     Deficiency A-ase     


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Date index: 2024-05-03
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