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Congenital afibrinogenaemia Deficiency AC globulin
DAF syndrome
Deficiency
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
G-6-p-d deficiency
G6PD deficiency
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
Labile
Lipid histiocytosis
Lipoid histiocytosis
Mobility deficiency
Mobility difficulty
Mobility disability
Mobility impairment
Niemann-Pick disease
PK
Proaccelerin
Prothrombin
Pyruvate kinase
Sphingomyelin lipidosis
Sphingomyelinase deficiency
Sphingomyelinase level
Stable
Stuart-Prower
Triose-phosphate isomerase deficiency
V
VII
X
XII
XIII

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

DAF syndrome | lipid histiocytosis | lipoid histiocytosis (classical phosphatide) | Niemann-Pick disease | sphingomyelin lipidosis | sphingomyelinase deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
ziekte van Niemann-Pick
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
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]
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
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Sphingomyelinase level
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
bepalen van sfingomyelinase
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
obesitas als gevolg van melanocortine-4-receptordeficiëntie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
3-methylglutaconzuuracidurie type 7
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [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]
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'
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
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
beperkte mobiliteit | mobiele beperking
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]


Anderen hebben gezocht naar : congenital afibrinogenaemia deficiency ac globulin     daf syndrome     deficiency of factor     g6pd deficiency     hageman     niemann-pick disease     sphingomyelinase level     stuart-prower     deficiency     fibrin-stabilizing     fibrinogen     g-6-p-d deficiency     glucose 6-dehydrogenase deficiency     glucose-6-phosphate dehydrogenase deficiency     hexokinase deficiency     labile     lipid histiocytosis     lipoid histiocytosis     mobility deficiency     mobility difficulty     mobility disability     mobility impairment     proaccelerin     prothrombin     pyruvate kinase     sphingomyelin lipidosis     sphingomyelinase deficiency     stable     triose-phosphate isomerase deficiency     Sphingomyelinase deficiency     


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Date index: 2024-01-01
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