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Aarskog
Cockayne
De Lange
Dubowitz
Dysostosis mandibulo-facialis
Dysostosis mandibulofacialis
Franceschetti
Holt-Oram
Klippel-Trenaunay-Weber
Manisch depressief syndroom
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom van
Syndroom van Franceschetti
Syndroom van Naegeli-Franceschetti-Jadassohn
TAR-syndroom
Treacher Collins
Trombocytopenie met ontbreken van radius
VATER-syndroom

Traduction de «Syndroom van Franceschetti » (Néerlandais → Français) :

syndroom van Franceschetti

érosion récidivante de la membrane antérieure de la cornée


syndroom van | Franceschetti | syndroom van | Treacher Collins

Syndrome de:Franceschetti | Treacher Collins


dysostosis mandibulofacialis | syndroom van Franceschetti

syndrome de Franceschetti et Zwahlen


dysostosis mandibulo-facialis | syndroom van Franceschetti

dysostose mandibulo-faciale


syndroom van Naegeli-Franceschetti-Jadassohn

syndrome de Naegeli-Franceschetti-Jadassohn




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: 2020-12-12
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