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Aarskog
Benedikt
Chorioretinitis centralis serosa
Claude
Cockayne
De Lange
Dubowitz
Foville
Holt-Oram
Klippel-Trenaunay-Weber
Millard-Gubler
Nagel-patella
Noonan
Oenococcus kitaharae
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
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 Kitahara
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Wallenberg
Weber
Ziektebeeld

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

chorioretinitis centralis serosa | syndroom van Kitahara

Kitahara syndrome




syndroom van Bernard | syndroom van Horner | syndroom van Horner-Bernard

Bernard-Horner syndrome


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


syndroom (van) | Benedikt | syndroom (van) | Claude | syndroom (van) | Foville | syndroom (van) | Millard-Gubler | syndroom (van) | Wallenberg | syndroom (van) | Weber

Syndrome:Benedikt | Claude | Foville | Millard-Gubler | Wallenberg | Weber


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)

'syndroom van kitahara' ->

Date index: 2022-08-12
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