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Translation of "Hypoplasie " (French → English) :
TERMINOLOGY
see also In-Context Translations below hypoplasie | développement insuffisant d'un tissu ou d'un organe
hypoplasia | tissue or organ underdevelopment
UGENT - Medical terms -
UGENT - Medical terms -
hypoplasie pulmonaire primitive
Primary pulmonary hypoplasia
SNOMEDCT-BE (disorder) / 277656005
SNOMEDCT-BE (disorder) / 277656005
hypoplasie dermique en aires
Focal dermal hypoplasia
SNOMEDCT-BE (disorder) / 205573006
SNOMEDCT-BE (disorder) / 205573006
hypoplasie rénale
Contracted kidney
SNOMEDCT-BE (finding) / 236448000
SNOMEDCT-BE (finding) / 236448000
Aplasie et hypoplasie du cément Dent hypoplasique de Turner Dislocation du germe dentaire Hypoplasie de l'émail (néonatale) (post-natale) (prénatale) Odontodysplasie régionale
Aplasia and hypoplasia of cementum Dilaceration of tooth Enamel hypoplasia (neonatal)(postnatal)(prenatal) Regional odontodysplasia Turner's tooth
WORLD HEALTH ORGANIZATION ICD-10: K00.4
WORLD HEALTH ORGANIZATION ICD-10: K00.4
polymicrogyrie avec hypoplasie du nerf optique
A rare genetic syndrome with characteristics of severe developmental delay, neonatal hypotonia, seizures, optic nerve hypoplasia and distinct central nervous system malformations including extensive bilateral polymicrogyria, dysplastic or absent corp
SNOMEDCT-BE (disorder) / 771336003
SNOMEDCT-BE (disorder) / 771336003
syndrome de pseudoanodontie-hypoplasie maxillaire-genu valgum
Stoelinga de Koomen Davis syndrome
SNOMEDCT-BE (disorder) / 723442008
SNOMEDCT-BE (disorder) / 723442008
syndrome d'hypoplasie du radius-pouces triphalangés-hypospadias-progénie
This syndrome has manifestation of symmetric, nonopposable triphalangeal thumbs and radial hypoplasia. It has been described in eight patients (five females and three males) spanning generations of a family. The affected males also presented with hyp
SNOMEDCT-BE (disorder) / 716092007
SNOMEDCT-BE / 716092007
syndrome de microcéphalie-hypoplasie cérébelleuse-trouble de la conduction cardiaque
A rare genetic congenital anomalies/dysmorphic syndrome characterized by growth failure, global developmental delay, profound intellectual disability, autistic behavior, acquired second-degree heart block with bradycardia and vasomotor instability. H
SNOMEDCT-BE (disorder) / 764732004
SNOMEDCT-BE (disorder) / 764732004
syndrome d'hypoplasie péroné-cubitus-anomalies rénales
This syndrome has features of fibuloulnar dysostosis with renal anomalies. It has been described in two siblings born to nonconsanguinous parents. The syndrome is lethal at birth (respiratory failure). Clinical manifestations include ear and facial a
SNOMEDCT-BE (disorder) / 716094008
SNOMEDCT-BE (respiratory failure). Clinical manifestations include ear and facial a / 716094008
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Hypoplasie
Date index:2021-05-09 -
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