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Translation of "Dysplasia " (English → French) :
TERMINOLOGY
see also In-Context Translations below dysplasia | abnormality of development
dysplasie | malformation
UGENT - Medical terms -
UGENT - Medical terms -
Omodysplasia is a rare skeletal dysplasia characterised by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalised form (also referred to as micromelic dysplasia with disloca
omodysplasie
SNOMEDCT-BE / 725164008
SNOMEDCT-BE (disorder) / 725164008
A rare genetic immuno-osseous dysplasia disorder with characteristics of pre and post-natal growth retardation, hypotonia, borderline to moderate intellectual disability, retinal dystrophy, spondyloepiphyseal dysplasia (epiphyseal dysplasia, epiphyse
syndrome de Roifman
SNOMEDCT-BE (epiphyseal dysplasia, epiphyse / 773404000
SNOMEDCT-BE (disorder) / 773404000
Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome
syndrome de dysplasie spondylo-épiphysaire, dystrophie rétinienne, déficit immunitaire
SNOMEDCT-BE (epiphyseal dysplasia, epiphyse / 773404000
SNOMEDCT-BE (disorder) / 773404000
A rare familial skeletal dysplasia with characteristics of multiple epiphyseal dysplasia with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. A mutation in PTHR1 gene is responsible for this synd
syndrome d'Eiken
SNOMEDCT-BE (disorder) / 720863002
SNOMEDCT-BE (disorder) / 720863002
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
Multiple epiphyseal dysplasia with severe proximal femoral dysplasia
dysplasie épiphysaire multiple avec dysplasie fémorale sévère
SNOMEDCT-BE (disorder) / 763893008
SNOMEDCT-BE (disorder) / 763893008
Aortic valve dysplasia
dysplasie valvulaire aortique
SNOMEDCT-BE (disorder) / 253604004
SNOMEDCT-BE (disorder) / 253604004
A lethal skeletal dysplasia with characteristics of cloverleaf skull anomaly, facial dysmorphism, limb shortness, splenic hypo/aplasia and radiological anomalies including thin tubular bones with flared metaphyses and deficient calvarial mineralisati
ostéocraniosténose
SNOMEDCT-BE (disorder) / 722109008
SNOMEDCT-BE (disorder) / 722109008
Rare syndrome with characteristics of the combination of polyvalvular heart disease, short stature, facial anomalies and intellectual deficit. Dysplasia may involve the mitral, tricuspidal, aortic and pulmonary valves. Dysmorphic facial anomalies are
syndrome de la maladie cardiaque polyvalvulaire
SNOMEDCT-BE (disorder) / 723448007
SNOMEDCT-BE (disorder) / 723448007
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'Dysplasia'
Date index:2022-08-31 -
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