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Aarskog
Bèta-glucuronidasedeficiëntie
Cockayne
De Lange
Dubowitz
Holt-Oram
Klippel-Trenaunay-Weber
Manisch depressief syndroom
Maroteaux-Lamy
Morquio
Mucopolysaccharidose IV
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Sanfilippo
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Horner
Syndroom van Horner-Bernard
Syndroom van Morquio
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziektebeeld

Traduction de «syndroom van morquio » (Néerlandais → Français) :

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)

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)


mucopolysaccharidose IV | syndroom van Morquio

maladie de Morquio | maladie de Morquio-Brailsford | maladie de Morquio-Ulrich | mucopolysaccharidose de type IV






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 Bernard | syndroom van Horner | syndroom van Horner-Bernard

syndrome de Bernard | syndrome oculo-sympathique


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


syndroom (van) | Holt-Oram | syndroom (van) | Klippel-Trenaunay-Weber | syndroom (van) | nagel-patella | syndroom (van) | Rubinstein-Taybi | syndroom (van) | sirenomelie | TAR-syndroom [trombocytopenie met ontbreken van radius] | VATER-syndroom

Ostéo-onychodysostose Syndrome de:Holt-Oram | Klippel-Trénaunay-Weber | onycho-arthro-ostéodysplasie | Rubinstein-Taybi | sirénomélie | thrombopénie avec absence de radius | VATER


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




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Date index: 2021-07-08
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