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Aarskog
Cockayne
De Lange
Dominant erfelijk
Dubowitz
Holt-Oram
Klippel-Trenaunay-Weber
LBWC
Nagel-patella
Noonan
Prader-Willi
Recessief erfelijk
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sensorische neuropathie
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Adams
Syndroom van Adams-Stokes
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Horner
Syndroom van Horner-Bernard
Syndroom van Morgagni
Syndroom van Nelaton
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziekte van Adams-Stokes
Ziekte van Morvan
Ziektebeeld

Traduction de «Syndroom van Nelaton » (Néerlandais → Anglais) :

sensorische neuropathie | dominant erfelijk | sensorische neuropathie | recessief erfelijk | syndroom van Nelaton | ziekte van Morvan
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
syndroom | ziektebeeld
http://users.ugent.be/~rvdstic (...) (...) [HTML] [2018-01-01]
syndrome
http://users.ugent.be/~rvdstic (...) (...) [HTML] [2018-01-01]
http://users.ugent.be/~rvdstic (...) [HTML] [2018-01-01]
syndroom van Bernard | syndroom van Horner | syndroom van Horner-Bernard
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
Bernard-Horner syndrome
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
A.-F.syndrome | cystine storage disease
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
syndroom van Adams | syndroom van Adams-Stokes | syndroom van Morgagni | ziekte van Adams-Stokes
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
Adams-Stokes disease | Adams-Stokes syndrome | Spens syndrome
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Syndrome:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
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
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Syndrome:Holt-Oram | Klippel-Trénaunay-Weber | nail patella | Rubinstein-Taybi | sirenomelia | thrombocytopenia with absent radius [TAR] | VATER
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
LBWC (limb body wall complex)-syndroom
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Limb body wall complex
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Pseudohypoparathyroidism type Ia
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


D'autres ont cherché : aarskog     cockayne     dubowitz     holt-oram     lbwc     noonan     prader-willi     rubinstein-taybi     russell-silver     seckel     smith-lemli-opitz     tar-syndroom     vater-syndroom     de lange     dominant erfelijk     nagel-patella     recessief erfelijk     sensorische neuropathie     sirenomelie     syndroom     syndroom van abderhalden-fanconi     syndroom van adams     syndroom van adams-stokes     syndroom van bernard     syndroom van debré-fanconi     syndroom van debré-de toni-fanconi     syndroom van horner     syndroom van horner-bernard     syndroom van morgagni     syndroom van nelaton     trombocytopenie met ontbreken van radius     ziekte van adams-stokes     ziekte van morvan     ziektebeeld     Syndroom van Nelaton     


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Date index: 2022-10-19
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