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Aarskog
Alfa-L-iduronidase deficiëntie
Cockayne
De Lange
Dubowitz
Holt-Oram
Hurler
Hurler-Scheie
Klippel-Trenaunay-Weber
LBWC
Mucopolysaccharidose I
Mucopolysaccharidose I-S
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Scheie
Scheie syndroom
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziektebeeld

Vertaling van "Scheie syndroom " (Nederlands → Engels) :

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

Syndrome:Hurler | Hurler-Scheie | Scheie


alfa-L-iduronidase deficiëntie | mucopolysaccharidose I-S | Scheie syndroom

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


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

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




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

A.-F.syndrome | cystine storage disease


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: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

Syndrome:Holt-Oram | Klippel-Trénaunay-Weber | nail patella | Rubinstein-Taybi | sirenomelia | thrombocytopenia with absent radius [TAR] | VATER


LBWC (limb body wall complex)-syndroom

Limb body wall complex


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

Pseudohypoparathyroidism type Ia


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

A rare genetic, poly malformative syndrome with characteristics of progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous




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

'Scheie syndroom' ->

Date index: 2021-08-19
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