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Traduction de «Mucopolysaccharidosis type I » (Anglais → Français) :

mucopolysaccharidosis type I | mucopolysaccharidosis type I S | Scheie syndrome | MPS I S [Abbr.]

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maladie de Scheie | mucopolysaccharidose de type I | mucopolysaccharidose de type I S | MPS I-S [Abbr.]

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Hurler-Scheie syndrome | mucopolysaccharidosis type I | mucopolysaccharidosis type I H/S | MPS I-H/S [Abbr.]

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mucopolysaccharidose de type I | mucopolysaccharidose de type I H/S | syndrome de Hurler-Scheie | MPS I-H/S [Abbr.]

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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)

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

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Mucopolysaccharidosis, type I

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Mucopolysaccharidose, type I

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Mucopolysaccharidosis, type II

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Mucopolysaccharidose, type II

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Mucopolysaccharidosis

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mucopolysaccharidose

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Mucopolysaccharidosis, MPS-I

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mucopolysaccharidose type 1

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touch type | type quickly | type at speed | typing at speed

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taper vite

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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

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albinisme oculo-cutané type 1

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D'autres ont cherché : 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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Date index: 2023-10-03