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Angioma capillare et venosum calcificans
Angiomatosis meningo-oculofacialis
Congenital alveolar dysplasia
Congenital dysplasia of hip joint
Congenital ectodermal dysplasia
Congenital neuroectodermal dysplasia
Cutaneocerebral angioma
Dimitri-disease
Ectodermal dysplasia
Encephalotrigeminal angiomatosis
Encephalotrigeminal syndrome
Kalischer's syndrome
Krabbe's II syndrome
Neurocutaneous syndrome
Parkes Weber's syndrome
Siemens'syndrome
Sturge's disease
Sturge's syndrome
Sturge-Kalischer-Weber syndrome
Sturge-Weber disease
Sturge-Weber syndrome
Sturge-Weber-Dimitri syndrome
Vara
Weber-Dimitri syndrome

Translation of "congenital neuroectodermal dysplasia " (English → French) :

Sturge-Weber syndrome | Dimitri-disease | Kalischer's syndrome | Krabbe's II syndrome | Parkes Weber's syndrome | Sturge's syndrome | Sturge's disease | Sturge-Kalischer-Weber syndrome | Sturge-Weber disease | Sturge-Weber-Dimitri syndrome | Weber-Dimitri syndrome | angioma capillare et venosum calcificans | angiomatosis meningo-oculofacialis | congenital neuroectodermal dysplasia | cutaneocerebral angioma | encephalotrigeminal angiomatosis | encephalotrigeminal syndrome | neurocutaneous syndrome

syndrome de Sturge-Weber | angiomatose encéphalotrigéminée de Sturge-Weber-Krabbe | angiomatose méningo-oculo-faciale | angiomatose neuro-cutanée | angiomatose neuro-oculo-cutanée | maladie de Sturge-Weber-Krabbe | neuro-ectodermo-dysplasie congénitale | syndrome de Brushfield-Wyatt | syndrome neuro-cutané | syndrome de Parkes-Weber | syndrome de Sturge-Weber-Krabbe | syndrome de Weber-Dimitri
biologie > embryologie | médecine > sémiologie et pathologie
biologie > embryologie | médecine > sémiologie et pathologie


congenital ectodermal dysplasia | ectodermal dysplasia | Siemens'syndrome

syndrome de Christ-Siemens
IATE - Health
IATE - Health


congenital ectodermal dysplasia

syndrome ectodermique
IATE - Health
IATE - Health


Anteversion of femoral neck Congenital acetabular dysplasia Congenital coxa:valga | vara

Antéversion du col du fémur Coxa:valga | vara | congénitale | Dysplasie acétabulaire congénitale
WORLD HEALTH ORGANIZATION ICD-10: Q65.8
WORLD HEALTH ORGANIZATION ICD-10: Q65.8


Congenital alveolar dysplasia

syndrome de détresse respiratoire du nouveau-né
SNOMEDCT-BE (disorder) / 46775006
SNOMEDCT-BE (disorder) / 46775006


congenital dysplasia of hip joint

dysplasie congénitale de la hanche
IATE - Health
IATE - Health


A very rare congenital malformation of the digits with the absence of the middle phalanges (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families.

brachydactylie type A5
SNOMEDCT-BE (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families. / 720570007
SNOMEDCT-BE (disorder) / 720570007




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'congenital neuroectodermal dysplasia'

Date index:2021-12-09 -

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