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Translation of "hypoplasia " (English → French) :
TERMINOLOGY
see also In-Context Translations below hypoplasia | tissue or organ underdevelopment
hypoplasie | développement insuffisant d'un tissu ou d'un organe
UGENT - Medical terms -
UGENT - Medical terms -
Aplasia and hypoplasia of cementum Dilaceration of tooth Enamel hypoplasia (neonatal)(postnatal)(prenatal) Regional odontodysplasia Turner's tooth
Aplasie et hypoplasie du cément Dent hypoplasique de Turner Dislocation du germe dentaire Hypoplasie de l'émail (néonatale) (post-natale) (prénatale) Odontodysplasie régionale
WORLD HEALTH ORGANIZATION ICD-10: K00.4
WORLD HEALTH ORGANIZATION ICD-10: K00.4
A rare genetic developmental defect during embryogenesis syndrome with characteristics of postaxial polydactyly and other abnormalities of the hands and feet (for example brachydactyly, broad toes), hypoplasia and fusion of the vertebral bodies, as w
syndrome de polydactylie postaxiale-anomalies dentaires et vertébrales
SNOMEDCT-BE (for example brachydactyly, broad toes), hypoplasia and fusion of the vertebral bodies, as w / 773279006
SNOMEDCT-BE (disorder) / 773279006
A form of non-rhizomelic chondrodysplasia punctata, a primary bone dysplasia, with characteristics of hypoplasia of the distal phalanges of the fingers, nasal hypoplasia, epiphyseal stippling appearing in the first year of life, as well as mild and n
chondrodysplasie ponctuée avec brachytéléphalangie
SNOMEDCT-BE (disorder) / 778067002
SNOMEDCT-BE (disorder) / 778067002
A rare genetic ocular disease with characteristics of congenital nystagmus (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an
syndrome d'hypoplasie fovéale-cataracte présénile
SNOMEDCT-BE (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an / 778042000
SNOMEDCT-BE (disorder) / 778042000
A form of syndromic craniosynostosis with characteristics of craniosynostosis, mild facial dysmorphism (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a f
syndrome de craniosynostose-calcifications intracrâniennes
SNOMEDCT-BE (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a f / 720816004
SNOMEDCT-BE (disorder) / 720816004
A subtype of junctional epidermolysis bullosa (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A ge
epidermolyse bulleuse jonctionnelle type non-Herlitz
SNOMEDCT-BE (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A ge / 724225008
SNOMEDCT-BE (disorder) / 724225008
Nail-patella syndrome is a rare hereditary patellar dysostosis with characteristics of nail hypoplasia or aplasia, aplastic or hypoplastic patellae, elbow dysplasia, and the presence of iliac horns as well as renal and ocular anomalies.
syndrome nail-patella
SNOMEDCT-BE (disorder) / 22199006
SNOMEDCT-BE (disorder) / 22199006
A chromosomal anomaly with characteristics of severe developmental delay and/or intellectual disability, typical facial dysmorphic features, brain anomalies, seizures, cleft palate, clubfeet, nail hypoplasia and congenital heart disease.
syndrome de microdélétion 1q41q42
SNOMEDCT-BE (disorder) / 716515000
SNOMEDCT-BE (disorder) / 716515000
A very rare X-linked recessive disorder considered to be a severe variant of dyskeratosis congenita, characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.
syndrome de Hoyeraal-Hreidarsson
SNOMEDCT-BE (disorder) / 707276009
SNOMEDCT-BE (disorder) / 707276009
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'hypoplasia'
Date index:2022-04-09 -
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