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Dysostosis multiplex
Gargoylism
Hurler syndrome
Hurler's disease
Hurler's syndrome
Hurler-Scheie syndrome
Lipochondrodystrophy
MPS I
MPS I S
MPS I-H
Morquio
Mucopolysaccharidosis
Mucopolysaccharidosis I
Mucopolysaccharidosis type I
Mucopolysaccharidosis type I S
Mucopolysaccharidosis type I-H
Pfaundler-Hurler syndrome
Sanfilippo
Scheie syndrome
Touch type
Type at speed
Type quickly
Typing at speed

Translation of "Mucopolysaccharidosis type I " (English → French) :

mucopolysaccharidosis type I | mucopolysaccharidosis type I S | Scheie syndrome | MPS I S [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
maladie de Scheie | mucopolysaccharidose de type I | mucopolysaccharidose de type I S | MPS I-S [Abbr.]
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Hurler-Scheie syndrome | mucopolysaccharidosis type I | mucopolysaccharidosis type I H/S | MPS I-H/S [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
mucopolysaccharidose de type I | mucopolysaccharidose de type I H/S | syndrome de Hurler-Scheie | MPS I-H/S [Abbr.]
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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]
dysostose multiple | gargoylisme | lipochondrodystrophie | maladie de Hurler | mucopolysaccharidose de type I | syndrome de Hurler | syndrome de Pfaundler-Hurler | MPS I [Abbr.] | MPS I-H [Abbr.]
IATE - Health
IATE - Health
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]
Carence en bêta-glucoronidase Mucopolysaccharidoses, type III, IV, VI, VII Syndrome de:Maroteaux-Lamy (léger) (sévère) | Morquio (-semblable à) (classique) | Sanfilippo (type B) (type C) (type D)
WORLD HEALTH ORGANIZATION ICD-10: E76.2
WORLD HEALTH ORGANIZATION ICD-10: E76.2
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Mucopolysaccharidosis, type I
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Mucopolysaccharidose, type I
WORLD HEALTH ORGANIZATION ICD-10: E76.0
WORLD HEALTH ORGANIZATION ICD-10: E76.0
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Mucopolysaccharidosis, type II
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Mucopolysaccharidose, type II
WORLD HEALTH ORGANIZATION ICD-10: E76.1
WORLD HEALTH ORGANIZATION ICD-10: E76.1
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Mucopolysaccharidosis
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
mucopolysaccharidose
SNOMEDCT-BE (disorder) / 11380006
SNOMEDCT-BE (disorder) / 11380006
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Mucopolysaccharidosis, MPS-I
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
mucopolysaccharidose type 1
SNOMEDCT-BE (disorder) / 75610003
SNOMEDCT-BE (disorder) / 75610003
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
touch type | type quickly | type at speed | typing at speed
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
taper vite
skill
Aptitude
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]
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]
albinisme oculo-cutané type 1
SNOMEDCT-BE (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 / 765146000
SNOMEDCT-BE (disorder) / 765146000
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Others have searched : hurler syndrome    hurler's disease    hurler's syndrome    hurler-scheie syndrome    mps    mps i-h    mps i-h s    morquio    pfaundler-hurler syndrome    sanfilippo    scheie syndrome    dysostosis multiplex    gargoylism    lipochondrodystrophy    touch type    type at speed    type quickly    typing at speed    Mucopolysaccharidosis type I    


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'Mucopolysaccharidosis type I'

Date index:2021-05-03 -

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