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Aarskog
Alfa-L-iduronidase deficiëntie
Cockayne
De Lange
Dubowitz
Dysostosis multiplex
Hurler
Hurler-Scheie
Hurler-syndroom
I-celziekte
Lipochondrodystrofie
Manisch depressief syndroom
Mucolipidose II
Mucolipidose III
Mucopolysaccharidose I
Noonan
Prader-Willi
Pseudosyndroom van Hurler
Robinow-Silverman-Smith
Russell-Silver
Scheie
Seckel
Smith-Lemli-Opitz
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Ziektebeeld

Traduction de «hurler-syndroom » (Néerlandais → Français) :

syndroom van | Hurler | syndroom van | Hurler-Scheie | syndroom van | Scheie

Syndrome de:Hurler | Hurler-Scheie | Scheie


dysostosis multiplex | Hurler-syndroom | lipochondrodystrofie

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.]


alfa-L-iduronidase deficiëntie | Hurler/Scheie syndroom | mucopolysaccharidose I

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






syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi

diabète rénal gluco-phosphoaminé | syndrome de De Toni-Debré-Fanconi


syndroom van | Aarskog | syndroom van | Cockayne | syndroom van | de Lange | syndroom van | Dubowitz | syndroom van | Noonan | syndroom van | Prader-Willi | syndroom van | Robinow-Silverman-Smith | syndroom van | Russell-Silver | syndroom van | Seckel | syndroom van | Smith-Lemli-Opitz

Syndrome de:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz


mucolipidose II [I-celziekte] | mucolipidose III [pseudosyndroom van Hurler]

Mucolipidose II [maladie à inclusion cellulaire] Mucolipidose III [polydystrophie de type Hurler]


SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom

syndrome d'hypertrophie segmentaire-lipomatose-malformation artérioveineuse-naevus épidermique


AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia

pseudohypoparathyroïdie type 1A




datacenter (28): www.wordscope.be (v4.0.br)

'hurler-syndroom' ->

Date index: 2024-10-24
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