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Blood
Congenital afibrinogenaemia Deficiency AC globulin
Constituency assistant
Deficiency of factor I
Dysostosis multiplex
Element of group VII
Fibrin-stabilizing
Fibrinogen
Gargoylism
Hageman
Hurler syndrome
Hurler's disease
Hurler's syndrome
II
Labile
Lipochondrodystrophy
MLA's assistant
MP
MP's personal assistant
MPS I
MPS I-H
MPS VII
Morquio
Mucopolysaccharidosis I
Mucopolysaccharidosis type I-H
Mucopolysaccharidosis type VII
Parliamentary assistant
Pfaundler-Hurler syndrome
Proaccelerin
Prothrombin
Sanfilippo
Sly disease
Sly syndrome
Stable
Stuart-Prower
V
VII
X
XII
XIII

Traduction de «mps vii » (Anglais → Néerlandais) :

mucopolysaccharidosis type VII | Sly disease | Sly syndrome | MPS VII [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
beta-glucuronidase deficiëntie | mucopolysaccharidose VII | Sly syndroom
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Blood (WBC) screen for MPS type VII
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
screenen op mucopolysacharidose VII in leukocyten in bloed
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A group of tyrosine related oculocutaneous albinism (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
oculocutaan albinisme type 1
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
dysostosis multiplex | gargoylism | Hurler syndrome | Hurler's disease | Hurler's syndrome | lipochondrodystrophy | mucopolysaccharidosis I | mucopolysaccharidosis type I-H | Pfaundler-Hurler syndrome | MPS I [Abbr.] | MPS I-H [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
dysostosis multiplex | Hurler-syndroom | lipochondrodystrofie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Mucopolysaccharidosis, MPS-I
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
mucopolysaccharidose type 1
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
element of group VII
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
elementen uit groep VII
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome:Maroteaux-Lamy (mild)(severe) | Morquio(-like)(classic) | Sanfilippo (type B)(type C)(type D)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
bèta-glucuronidasedeficiëntie | mucopolysaccharidose, type III, IV, VI, VII | syndroom (van) | Maroteaux-Lamy (licht)(ernstig) | syndroom (van) | Morquio(-achtig)(klassiek) | syndroom (van) | Sanfilippo (type B)(type C)(type D)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
MLA's assistant | MP's personal assistant | constituency assistant | parliamentary assistant
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
medewerker van een lid van het parlement | medewerkster van een lid van het parlement | parlementair assistent | parlementair medewerker
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]
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]
Marrakesh Protocol to the General Agreement on Tariffs and Trade 1994 [ MP ]
https://www.termdat.bk.admin.c (...) (...) [HTML] [2018-01-01]
Protocol van Marrakesh bij de Algemene Overeenkomst inzake Tarieven en Handel [ MP | PM ]
https://www.termdat.bk.admin.c (...) (...) [HTML] [2018-01-01]
https://www.termdat.bk.admin.c (...) [HTML] [2018-01-01]


D'autres ont cherché : congenital afibrinogenaemia deficiency ac globulin     deficiency of factor     hageman     hurler syndrome     hurler's disease     hurler's syndrome     mla's assistant     mp's personal assistant     mps i-h     mps vii     morquio     pfaundler-hurler syndrome     sanfilippo     sly disease     sly syndrome     stuart-prower     constituency assistant     dysostosis multiplex     element of group vii     fibrin-stabilizing     fibrinogen     gargoylism     labile     lipochondrodystrophy     parliamentary assistant     proaccelerin     prothrombin     stable     


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Date index: 2022-12-09
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